The authors thank the ESRF for beamtime.

NOTE: The production, purification, and crystallization of GCSH are described in Supplementary File 1.
1. Brief description of the offline preparation and crystal mounting
<ol>
	<li>Position a nylon loop or another crystal mounting support already fixed to a SPINE pin under one or more crystals and lift them out of the precipitation solution (20 &#181;L of 0.5 M sodium formate pH 4.0 + 25 &#181;L of protein solution).
	<ol>
		<li>Remove the bulk liquid around the crystal(s) by touching the mount with a paper wick to suck off any excess liquid.</li>
	</ol>
	</li>
	<li>Soak the crystal(s) in the cryoprotective solution containing the precipitation solution plus 30% glycerol; then, remove both the crystal support and the crystal(s).
	<ol>
		<li>Remove the bulk liquid around the crystal(s) by touching the mount with a paper wick to suck off any excess liquid.</li>
	</ol>
	</li>
	<li>Plunge the mount into a SPINE vial filled with liquid nitrogen and store it, along with any other crystals similarly prepared, in a European Molecular Biology Laboratory (EMBL)/ESRF sample changer puck9 at liquid nitrogen temperature. 
	NOTE: The crystal(s) are stable in this condition until the beamtime is available.</li>
</ol>
2. Requesting beamtime on MASSIF-1
<ol>
	<li>Request beamtime as early as possible on the ESRF homepage (at http://www.esrf.eu/UsersAndScience/UserGuide/Applying). 
	NOTE: There are a number of possible modes of access to the ESRF MX beamlines. Laboratories can apply collectively as part of a Block Allocation Group (BAG), to have beamtime allocated for 2 years. If groups wish to apply individually, they can apply for rolling access, which allows them rapid access to the beamlines after peer review. The group&#8217;s proposal will be reviewed and cleared by the ESRF Safety Group who may request additional details. If the proposal is accepted, an experiment number and password will be communicated. Proprietary research can be performed by purchasing beamtime.</li>
	<li>Complete the required safety training online (at http://www.esrf.eu/UsersAndScience/UserGuide/Preparing/SafetyTraining).</li>
	<li>Book beamtime on the MASSIF-1 Calendar. 
	NOTE: It is possible to book up to a maximum of 50 sample holders to be analyzed per shift.</li>
	<li>Fill in the A-form to declare a mail-in experiment (http://www.esrf.eu/UsersAndScience/UserGuide/Preparing/new-a-form), along with the required safety information, for the samples that are to be measured.</li>
</ol>
3. Creation of a diffraction plan in ISPyB
NOTE: The diffraction plan holds all the information needed for a sample in ISPyB and can contain additional information to tailor the experiment performed for each sample.
<ol>
	<li>Open ISPyB (at https://exi.esrf.fr/).</li>
	<li>Choose MX experiments.</li>
	<li>Log in with the experiment number and password.</li>
	<li>Click on Shipment | Add new and provide the necessary information. Click Save.</li>
	<li>Click Add parcel and fill in the information requested. Click Save.</li>
	<li>Then, click Add container, give the puck barcode as the name, and choose SPINE puck. Click Save.</li>
	<li>Click on the container symbol and Edit, and fill in the necessary information, like protein name, preferred workflow, crystal position in the puck, etc., concerning the samples.</li>
	<li>Choose the protein (for example, GCSH or lysozyme) that has been approved by the ESRF safety group.</li>
	<li>Enter a unique sample name to identify each individual sample. It is possible to optionally scan the pin barcode. The rest of the information below is optional.</li>
	<li>Enter the optional information.
	<ol>
		<li>For each individual sample, enter the experiment type (i.e., MXPressE_SAD, SCORE, or MXPressO, etc., default MXPressE) under Exp. Type. This defines which automatic workflow will be used to process each crystal. Given that the GCSH crystals are needles, choose MXPressP.</li>
		<li>Enter a space group (for example, P1, C2, or P212121), if known. If present, this will be used for data collection strategy calculations and by the automatic data processing pipelines available.</li>
		<li>Enter the desired resolution (default: dmin = 2.0&#8197;&#197;). This defines the crystal-to-detector distance for the initial mesh scans, characterization, and default data collection.</li>
		<li>Set the desired threshold resolution (for example, 1.5 &#197; or 2.3&#197;), to prevent the collection of full datasets from crystals which do not diffract to this limit. This can save data storage space and analysis time.</li>
		<li>Set the required completeness (default: 0.99). Set the required multiplicity (default: 4). If more than one crystal is contained on the sample support, set the maximum number of crystals to be analyzed. The default value is 1 or 5 for MXPressP.</li>
		<li>Select the appropriate beam size (default: 50&#8197;&#181;m). If a specific value is not selected, the X-ray-centering and data collection strategy calculations will be performed with a beam size of 50 &#181;m. 
		NOTE: During any subsequent collection of complete data sets, the beam size will be adapted automatically.</li>
		<li>Put in the space group, if known, in the forced space group column. Set the radiation-sensitivity of the crystals (0.5&#8211;2.0 for low to high sensitivity, with a default value of 1).</li>
	</ol>
	</li>
	<li>If desired, set the total rotation angle to be collected for the full dataset collection (default: the total rotation angle determined by eEDNA).</li>
	<li>Save the values. Click on Return to Shipments. Press Send Shipment to ESRF.</li>
	<li>Print the shipping label and send the samples. Users should arrange a pickup with a courier, using the ESRF account details. 
	NOTE: It is very important to select Include return label to allow the seamless return of samples (see https://www.esrf.eu/MXDewarReimbursement).</li>
</ol>
4. Data collection, viewing, and retrieval
NOTE: On the day of the experiment, samples are transferred to the MASSIF-1 High Capacity Dewar (HCD). Beamline scientists then launch the data collection, which can be followed by users remotely. For each different sample type users receive an e-mail informing them that the data collection has started. As previously noted, the execution of all steps in all workflows can be followed online and in real-time by the user via ISPyB, from which the results can be viewed and downloaded.
<ol>
	<li>For each sample analyzed, examine the results of the automatic experiment in ISPyB (https://exi.esrf.fr/).
	<ol>
		<li>Log in, using the experiment number and password, and click on the desired experimental session at ID30A-1.</li>
		<li>Select the preferred (top-scoring) autoprocessing pipeline (for example, Grenades or XDS_APP) and download the data written out in the correct space group with the highest completeness and highest resolution by clicking on Last Collect Results and, then, Download. 
		NOTE: All mesh, line, and characterization images are in a subdirectory for each sample, called /MXPressE_01. The ESRF automatically runs five separate processing packages, namely EDNA_proc12, Grenades12, XDS_APP14, autoPROC15, and XIA216. Data integration is based on XDS, with the exception of XIA2, which is based on DIALS. All packages are also run in anomalous and nonanomalous modes, allowing the automatic detection of an anomalous signal, if present in the data, to be used in SAD phasing protocols. Each package uses different parameters and decision trees, meaning that some packages run better with certain samples. However, this can make for a large number of results when the number of packages and possible space groups is accounted for. The results are, therefore, ranked based roughly on resolution and other quality metrics, such as Rmerge in the lowest resolution shell, CC(1/2), and completeness. This is aimed at guiding the user to the best data sets, but all possible space groups and results should be inspected carefully.</li>
	</ol>
	</li>
	<li>Unzip the downloaded folder, which will include all log files and unmerged XDS_ASCII.HKL and merged and scaled .mtz files. 
	NOTE: In case the structure (in PDB format) of the protein of interest or a close homolog was uploaded to ISPyB at the start of the experiment, the autoprocessing pipeline at ESRF will automatically perform a molecular replacement (MR) run using this structure as the search model on the best scoring solution. The results of the MR pipeline are displayed in ISPyB and can be found in the processed data folder (for example, /data/visitor/mx2112/id30a1/20180711/PROCESSED_DATA/GCSH/GCSH-x5/autoprocessing_GCSH-x5_run1_1/grenades_fastproc/user_nohet.pdb_mrpipe_dir/). Here, the final model will be named coot1.pdb and the reflection data sidechains.mtz. Note that the pipeline might reduce the symmetry of the cell (primitive cell reduction) in order to increase the likelihood of finding a solution. In the case here, the MR pipeline wrote out the solution in a monoclinic cell (C2) rather than in an orthorhombic cell (C2221). Details on how to perform a molecular replacement run manually (exemplified for the second best-scoring autoprocessing solution) are included in the Supplementary Files.</li>
</ol>

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W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fully+automatic+characterization+and+data+collection+from+crystals+of+biological+macromolecules.">Fully automatic characterization and data collection from crystals of biological macromolecules.</a> Acta Crystallographica Section D Biological Crystallography. 71 (8), 1757-1767 (2015).</li><li>Cipriani, F., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=CrystalDirect:+a+new+method+for+automated+crystal+harvesting+based+on+laser-induced+photoablation+of+thin+films.">CrystalDirect: a new method for automated crystal harvesting based on laser-induced photoablation of thin films.</a> Acta Crystallographica Section D Biological Crystallography. 68, 1393-1399 (2012).</li><li>Nurizzo, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=RoboDiff:+combining+a+sample+changer+and+goniometer+for+highly+automated+macromolecular+crystallography+experiments.">RoboDiff: combining a sample changer and goniometer for highly automated macromolecular crystallography experiments.</a> Acta Crystallographica Section D Structural Biology. 72 (8), 966-975 (2016).</li><li>Bowler, M. W., Svensson, O., Nurizzo, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fully+automatic+macromolecular+crystallography:+the+impact+of+MASSIF-1+on+the+optimum+acquisition+and+quality+of+data.">Fully automatic macromolecular crystallography: the impact of MASSIF-1 on the optimum acquisition and quality of data.</a> Crystallography Reviews. 22 (4), 233-249 (2016).</li><li>Brockhauser, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+use+of+workflows+in+the+design+and+implementation+of+complex+experiments+in+macromolecular+crystallography.">The use of workflows in the design and implementation of complex experiments in macromolecular crystallography.</a> Acta Crystallographica Section D Biological Crystallography. 68 (8), 975-984 (2012).</li><li>Svensson, O., Gilski, M., Nurizzo, D., Bowler, M. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Multi-position+data+collection+and+dynamic+beam+sizing:+recent+improvements+to+the+automatic+data-collection+algorithms+on+MASSIF-1.">Multi-position data collection and dynamic beam sizing: recent improvements to the automatic data-collection algorithms on MASSIF-1.</a> Acta Crystallographica Section D Structural Biology. 74, 433-440 (2018).</li><li>Cipriani, F., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Automation+of+sample+mounting+for+macromolecular+crystallography.">Automation of sample mounting for macromolecular crystallography.</a> Acta Crystallographica Section D Biological Crystallography. 62 (10), 1251-1259 (2006).</li><li>Delageniere, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=ISPyB:+an+information+management+system+for+synchrotron+macromolecular+crystallography.">ISPyB: an information management system for synchrotron macromolecular crystallography.</a> Bioinformatics. 27 (22), 3186-3192 (2011).</li><li>Monaco, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Automatic+processing+of+macromolecular+crystallography+X-ray+diffraction+data+at+the+ESRF.">Automatic processing of macromolecular crystallography X-ray diffraction data at the ESRF.</a> Journal of Applied Crystallography. 46 (3), 804-810 (2013).</li><li>Kikuchi, G., Motokawa, Y., Yoshida, T., Hiraga, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Glycine+cleavage+system:+reaction+mechanism,+physiological+significance,+and+hyperglycinemia.">Glycine cleavage system: reaction mechanism, physiological significance, and hyperglycinemia.</a> Proceedings of the Japan Academy. Series B, Physical and Biological Sciences. 84 (7), 246-263 (2008).</li><li>Sparta, K. M., Krug, M., Heinemann, U., Mueller, U., Weiss, M. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=XDSAPP2.0.">XDSAPP2.0.</a> Journal of Applied Crystallography. 49 (3), 1085-1092 (2016).</li><li>Vonrhein, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Data+processing+and+analysis+with+the+autoPROC+toolbox.">Data processing and analysis with the autoPROC toolbox.</a> Acta Crystallographica Section D Biological Crystallography. 67 (4), 293-302 (2011).</li><li>Winter, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=xia2:+an+expert+system+for+macromolecular+crystallography+data+reduction.">xia2: an expert system for macromolecular crystallography data reduction.</a> Journal of Applied Crystallography. 43 (1), 186-190 (2010).</li><li>Higashiura, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=High-resolution+X-ray+crystal+structure+of+bovine+H-protein+at+0.88+&#197;+resolution.">High-resolution X-ray crystal structure of bovine H-protein at 0.88 &#197; resolution.</a> Acta Crystallographica Section D Biological Crystallography. 66 (6), 698-708 (2010).</li><li>Sanishvili, R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+7+&#181;m+mini-beam+improves+diffraction+data+from+small+or+imperfect+crystals+of+macromolecules.">A 7 &#181;m mini-beam improves diffraction data from small or imperfect crystals of macromolecules.</a> Acta Crystallographica Section D Biological Crystallography. 64 (4), 425-435 (2008).</li><li>Bowler, M. 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The authors have nothing to disclose.

Fully automatic beamlines provide automated characterization and data collection from large numbers of macromolecular crystals without the presence of a scientist, either at the beamline or remotely, being required. Using completely automated beamlines has many advantages compared to manual operation. For example, the automated sample centering, based on X-ray mesh and line scans, is more precise than that performed with the human eye as it is not affected by thermal or optical effects. Indeed, these mesh and line scans provide additional data (i.e., detailed dimensions of the crystal and the best diffracting region of the crystal) which are important in determining the correct beam size to use for data collection&#8212;especially for small crystals18&#8212;and often result in an improved quality of the obtained diffraction data. Moreover, by taking advantage of the user-defined parameters in the setup of automatic experiments, the steps in specific workflows can be tailored to best suit the system under study, thus further optimizing the experiment success rate.
Taking together, the reliability of the workflows available, the straightforward access to the beamline (users self-schedule, using a calendar [see above]), and the fully automated approach of MASSIF-1 provides a rigorous, high-throughput, and time-saving alternative to classical hands-on MX experiments and the potential to implement more advanced procedures and applications into automatic workflows. In the near future, crystal cartography in 3D19 will be implemented to improve the accuracy of X-ray centering, while more complex protocols, such as crystal dehydration experiments20, will be automated. It is hoped that fully autonomous data collection will become a standard method in MX, providing high-quality data for small-molecule fragment screens, optimizing the screening of large numbers of poorly diffracting crystals and automatically providing phase information to solve crystal structures de novo. In combination with developments in the automated harvesting of crystals21, the possibility of protein crystal structure solution as an automated service could well become a reality.

Determining the three-dimensional structure of specific proteins is crucial in biology. The information that is derived from doing so sheds light on the biological function and on the shape and specificity of active and/or binding sites contained in the molecule under study. In many cases, this allows mechanisms of action to be determined or, where appropriate, potential therapeutic molecules to be developed. MX is the technique most commonly used to obtain structural information, but a bottleneck is the determination of the optimal conditions to obtain well-diffracting crystals. Therefore, crystallization trials are carried out in numerous different conditions and are then screened, to find the best crystals to be used for diffraction data collection. The automation of the setup of crystallization trials1 has clearly helped in this regard. However, the subsequent steps (i.e., crystal mounting, diffraction screening, and diffraction data collection) are usually carried out manually, taking up a lot of time, effort, and resources. The automation of diffraction screening and data collection would, therefore, mean an enormous gain in time and efficiency.
Diffraction screening and data collection in MX is most often carried out at synchrotron MX beamlines at which automation has largely facilitated this process. However, in most cases, it is necessary for the scientist to be present at the beamline during an experiment or to operate it remotely. Recently, a new generation of completely automated MX beamlines has been developed2. Here, users do not need to be present, either physically or remotely, during an experimental session. This allows scientists to spend more time on less routine tasks, rather than spending entire days, and often nights, screening crystals and collecting diffraction data. The world&#39;s first fully automated beamline is the Massively Automated Sample Selection Integrated Facility (MASSIF-1, ID30A-1)2,3 at the European Synchrotron Radiation Facility (ESRF). It has a unique sample environment in which a high-capacity sample-containing dewar operates in tandem with a robotic sample changer that also acts as the beamline&#39;s goniometer4,5. MASSIF-1 is an undulator beamline equipped with a single-photon-counting hybrid pixel detector6, that operates at a fixed wavelength of 0.969&#8197;&#197; (12.84&#8197;keV) with an intense X-ray beam (2 x 1012 photons/s). The beam size at the sample position can be adjusted between a minimum of 10 &#181;m (round beam) to a maximum of 100 &#181;m x 65 &#181;m (horizontal by vertical beam size). On average, the beamline can process, in a completely automatic fashion (see below), 120 crystals in 24 h. The operation of the beamline is based on a series of workflows7, each of which takes intelligent decisions based on the outcome of previous steps in the workflow, to ensure the measurement of the best possible data from the sample under study. In particular, the evaluation of the diffraction characteristics of an individual sample takes into account crystal volume and flux and ensures, where the crystal is larger than the X-ray beam, that only the best region of the crystal is used for subsequent data collection. Diffraction data sets are, thus, optimized for maximum resolution with minimized radiation damage2,3. Demanding data collection protocols, such as pseudo-helical (multi-position) data collection strategies for both native and single-wavelength anomalous diffraction (SAD) data collection, are also available8.
Completely automatic experiments at MASSIF-1 involve cryocooling and mounting the crystals on a magnetic sample mount suitable for the desired beamline equipment standard pins SPINE9, entering the desired experimental parameters in the &#39;diffraction plan&#39; table in the Integrated System for Protein Crystallography beamlines (ISPyB)10, a web-based information management system for MX experiments, and sending the samples to the beamline. At the ESRF, all costs of the transport of the samples to/from the beamline are supported by the ESRF User Office (see the website of the ESRF11 for details). At MASSIF-1, no restrictions are placed on the loop size or crystal quality. When choosing a diffraction plan for a given crystal, the user can either use default settings or choose from specific workflows, which can be customized for each sample. Several preprogrammed workflows are available. In the MXPressE3 workflow, the sample-containing loop is first aligned to the sample position using optical centering. Then, X-ray-based centering ensures that the best region of the crystal is centered to the X-ray beam. Data collection strategies are then calculated using eEDNA, a framework for developing plugin-based applications especially for online data analysis in the X-ray experiments field, taking into account crystal volume and the real-time flux at the beamline. Following the collection of a full diffraction data set, this is then processed using a series of automatic data processing pipelines12 and the results are made available for inspection and download in ISPyB. The MXPressE SAD3 workflow is aimed at selenomethionine-containing crystals of the target protein and exploits the fact that the operating energy of MASSIF-1 is just above the Se K edge. Here, the MXPressE eEDNA data collection strategy is optimized for SAD data collection (i.e., high redundancy, and with the resolution set to where the Rmerge between Bijvoet pairs is below 5%). To screen the diffraction properties of a series of crystals without subsequent data collection, the MXScore3 workflow can be used to produce a full quality assessment of the crystals analyzed. In the MXPressI3 workflow, 180&#176; of rotation data are collected using 0.2&#176; oscillations and using the starting phi angle and the resolution determined by an eEDNA strategy. MXPressO3 includes a preobserved resolution into the workflow (default: dmin = 2 &#197;). To make an initial assessment of the crystals resulting from a crystallization trial, the MXPressM3&#160;workflow is offered. This performs a high-dose mesh scan over the widest orientation of sample support with no data collection or centering. Recently, two new experiment workflows, MXPressP and MXPressP_SAD, which perform pseudohelical data collections, have been implemented8. The execution of all steps in all workflows can be followed online and in real-time by the user, via ISPyB.
Here we show how to prepare a fully automated MX experiment at MASSIF-1 and how to retrieve and analyze the data resulting from the experiment. As an example, we use human mitochondrial glycine cleavage system protein H (GCSH). This lipoic acid-containing protein is part of the glycine cleavage system responsible for the degradation of glycine. This system further includes the P protein, a pyridoxal phosphate-dependent glycine decarboxylase, the T protein, a tetrahydrofolate-requiring enzyme, and the L protein, a lipoamide dehydrogenase. GCSH transfers the methylamine group of glycine from the P protein to the T protein. Defects in the H protein are the cause of nonketotic hyperglycinemia (NKH) in humans13.

<table><tbody><tr><td>Beamline MASSIF-1</td><td>ESRF</td><td></td><td></td></tr><tr><td>BL21DE3</td><td>New England Biolabs</td><td>C2527I</td><td></td></tr><tr><td>chloramphenicol</td><td>Roth</td><td>3886.1</td><td></td></tr><tr><td>Concentrators: Amicon Ultra-4 Ultracel -30K</td><td>Merck Millipore</td><td>UFC803024</td><td></td></tr><tr><td>Dialyzing membrane</td><td>Spectrumlabs</td><td>132655</td><td></td></tr><tr><td>DMSO</td><td>Sigma-Aldrich</td><td>D8418</td><td></td></tr><tr><td>Dnase</td><td>Roche</td><td>11284932001</td><td></td></tr><tr><td>DTT</td><td>Euromedex</td><td>EU0006-B</td><td></td></tr><tr><td>EDTA- free protease inhibitors</td><td>Roche</td><td>4,693,159,001</td><td></td></tr><tr><td>glycerol</td><td>VWR Chemicals Prolabo</td><td>14388.29T</td><td></td></tr><tr><td>His-trap HP</td><td>GE healthcare</td><td>17-5247-01</td><td></td></tr><tr><td>imidazole</td><td>Sigma-Aldrich</td><td>56750-500G</td><td></td></tr><tr><td>IPTG</td><td>Euromedex</td><td>EU0008-B</td><td></td></tr><tr><td>LB medium</td><td>Sigma-Aldrich</td><td>L3022</td><td></td></tr><tr><td>lipoic acid</td><td>Sigma-Aldrich</td><td>T5625</td><td></td></tr><tr><td>loop</td><td>Hampton Research</td><td>HR8-124</td><td></td></tr><tr><td>lysozyme</td><td>Roche</td><td>10 837 059 001</td><td></td></tr><tr><td>MonoQ 5/50 GL</td><td>GE healthcare</td><td>17-5166-01</td><td></td></tr><tr><td>NaCl</td><td>Fisher Chemical</td><td>S/3160/60</td><td></td></tr><tr><td>Sonicator vibra cell 75/15</td><td>SONICS</td><td></td><td></td></tr><tr><td>SPINE pucks</td><td>MiTeGen</td><td>SKU: M-CSM003-0001A</td><td></td></tr><tr><td>Tris base</td><td>Euromedex</td><td>26-128-3094-B</td><td></td></tr><tr><td>Sodium Formate</td><td>Sigma-Aldrich</td><td>1064430500</td><td></td></tr><tr><td>GCSH purification buffer</td><td>20 mM TRIS pH 8, 200 mM NaCl</td><td></td><td></td></tr><tr><td>GCSH cryo-protection buffer</td><td>0.25 M Sodium Formate pH 4, 30% glycerol</td><td></td><td></td></tr><tr><td>&lt;strong&gt;Programs:&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>MxCube</td><td></td><td>Gabadinho, J. et al. MxCuBE : a synchrotron beamline control environment customized for macromolecular crystallography experiments. Journal of Synchrotron Radiation. 17 (5), 700-707, doi: 10.1107/S0909049510020005 (2010)</td><td>local development</td></tr><tr><td>ISPyB</td><td>ESRF</td><td>Solange Delageni&amp;egrave;re, Patrice Brenchereau, Ludovic Launer, Alun W. Ashton, Ricardo Leal, St&amp;eacute;phanie Veyrier, Jos&amp;eacute; Gabadinho, Elspeth J. Gordon, Samuel D. Jones, Karl Erik Levik, Se&amp;aacute;n M. McSweeney, St&amp;eacute;phanie Monaco, Max Nanao, Darren Spruce, Olof Svensson, Martin A. Walsh, Gordon A. Leonard; ISPyB: an information management system for synchrotron macromolecular crystallography, Bioinformatics, Volume 27, Issue 22, 15 November 2011, Pages 3186-3192, https://doi-org.bdigitaluss.remotexs.co/10.1093/bioinformatics/btr535</td><td>local development</td></tr><tr><td>MXCube2</td><td>ESRF</td><td>Gabadinho, J. &lt;em&gt;et al.&lt;/em&gt; &lt;em&gt;MxCuBE&lt;/em&gt; : a synchrotron beamline control environment customized for macromolecular crystallography experiments. &lt;em&gt;Journal of Synchrotron Radiation&lt;/em&gt;. &lt;strong&gt;17&lt;/strong&gt; (5), 700-707, doi: 10.1107/S0909049510020005 (2010). De Santis, D., Leonard, G. Notiziario Neutroni e Luce di Sincrotrone,Consiglio Nazionale delle Ricerche. (19), 24-226 (2014).</td><td>local development</td></tr><tr><td>BES workflow server</td><td></td><td>Brockhauser, S. et al. The use of workflows in the design and implementation of complex experiments in macromolecular crystallography. Acta Crystallographica Section D Biological Crystallography. 68 (8), 975-984, doi: 10.1107/S090744491201863X (2012).</td><td></td></tr><tr><td>DOZOR</td><td>ESRF</td><td>Bourenkov and Popov, unpublished</td><td>local development</td></tr><tr><td>BLISS beamline control</td><td></td><td>Guijarro, M. et al. BLISS - Experiments Control for ESRF EBS Beamlines. Proceedings of the 16th Int. Conf. on Accelerator and Large Experimental Control Systems, ICALEPCS2017, Barcelona, Spain. doi: 10.18429/jacow-icalepcs2017-webpl05 (2018).</td><td>local development</td></tr><tr><td>AUTO processing of images</td><td></td><td>Monaco, S. et al. Automatic processing of macromolecular crystallography X-ray diffraction data at the ESRF. Journal of Applied Crystallography. &lt;strong&gt;46&lt;/strong&gt; (3), 804-810, doi: 10.1107/S0021889813006195 (2013)</td><td>local development</td></tr><tr><td>BEST and EDNA</td><td></td><td>Incardona, M.-F., Bourenkov, G.P., Levik, K., Pieritz, R.A., Popov, A.N., Svensson, O. EDNA : a framework for plugin-based applications applied to X-ray experiment online data analysis. Journal of Synchrotron Radiation. &lt;strong&gt;16&lt;/strong&gt; (6), 872-879, doi: 10.1107/S0909049509036681 (2009).</td><td>local development</td></tr><tr><td>CCP4</td><td></td><td>Winn, M.D. &lt;em&gt;et al.&lt;/em&gt; Overview of the &lt;em&gt;CCP&lt;/em&gt; 4 suite and current developments. &lt;em&gt;Acta Crystallographica Section D Biological Crystallography&lt;/em&gt;. &lt;strong&gt;67&lt;/strong&gt; (4), 235-242, doi: 10.1107/S0907444910045749 (2011).</td><td></td></tr><tr><td>Phaser MR</td><td></td><td>McCoy, A.J., Grosse-Kunstleve, R.W., Adams, P.D., Winn, M.D., Storoni, L.C., Read, R.J. &lt;em&gt;Phaser&lt;/em&gt; crystallographic software. &lt;em&gt;Journal of Applied Crystallography&lt;/em&gt;. &lt;strong&gt;40&lt;/strong&gt; (4), 658-674, doi: 10.1107/S0021889807021206 (2007).</td><td></td></tr><tr><td>Coot</td><td></td><td>Emsley, P., Cowtan, K. Coot: model-building tools for molecular graphics. &lt;em&gt;Acta Crystallogr D Biol Crystallogr&lt;/em&gt;. &lt;strong&gt;60&lt;/strong&gt;, 2126-32 (2004).</td><td></td></tr><tr><td>refmac5</td><td></td><td>Murshudov, G.N., Vagin, A.A., Dodson, E.J. Refinement of Macromolecular Structures by the Maximum-Likelihood Method. &lt;em&gt;Acta Crystallographica Section D&lt;/em&gt;. &lt;strong&gt;53&lt;/strong&gt;, 240--255 (1997).</td><td></td></tr><tr><td>Matthews</td><td></td><td>Matthews, B.W. Solvent content of protein crystals. Journal of Molecular Biology. 33 (2), 491-497 (1968).</td><td></td></tr></tbody></table>

fully autonomous characterization and data collection from crystals of biological macromolecules

High-brilliance X-ray beams coupled with automation have&#160;led to the use of synchrotron-based macromolecular X-ray crystallography (MX) beamlines for even the most challenging projects in structural biology. However, most facilities still require the presence of a scientist on site to perform the experiments. A new generation of automated beamlines dedicated to the fully automatic characterization of, and data collection from, crystals of biological macromolecules has recently been developed. These beamlines represent a new tool for structural biologists to screen the results of initial crystallization trials and/or the collection of large numbers of diffraction data sets, without users having to control the beamline themselves. Here we show how to set up an experiment for automatic screening and data collection, how an experiment is performed at the beamline, how the resulting data sets are processed, and how, when possible, the crystal structure of the biological macromolecule is solved.

The MXPressP workflow was used at the ESRF beamline MASSIF-1 to, fully automatically, mount, center in the X-ray beam, characterize, and collect full diffraction data sets from a series of crystals of human GCSH. The samples were mounted and the loop analyzed for an area to scan (Figure 1, left). After the diffraction analysis, four points were selected within the crystal for data collection (Figure 1, right). Subsequent processing by automated data analysis pipelines, including the MR pipeline, yielded high-quality datasets (Table 1) for which an MR solution was found. The latter allows users to rapidly evaluate whether the obtained dataset and the used search model are suitable for phasing by molecular replacement. In addition, the presence of ligands can be judged, thus permitting the user to focus only on the most promising datasets for further analysis. Manual structure determination by MR yielded a high-quality electron density map after a single automated refinement cycle (Figure 2a). For this dataset, the automated pipeline cut the data at a 1.32 &#197; resolution; however, users can still decide to cut the data at a lower resolution to arrive at different quality statistics (CC1/2, &#60;I/&#963;(I)&#62;, Rmeas) in the highest resolution shell. The crystal structure of human GCSH structure is similar to that of the bovine protein (3KlR)16.
Continuous electron density is visible for the entire amino acid chain, apart from the N-terminal histidine tag. Of the four substitutions that distinguish human and bovine GCSH, three are readily identifiable in the electron density (Ile/Val66, Asp/Glu98, and Leu/Phe149; Figure 2b-d). This is less clear for the Asp/Lys125 substitution for which the electron density of the side chain is only partially resolved due to flexibility (Figure 1e). The currently obtained model has Rwork and Rfree values of 20.4% and 23.8%, respectively, and can be further optimized by further cycles of automated and manual model building and refinement.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td></td>
			<td>GRENADES pipeline</td>
			<td>XDS_APP pipeline</td>
		</tr>
		<tr>
			<td colspan="3">Data collection and processing</td>
		</tr>
		<tr>
			<td>X-ray source / Beam line</td>
			<td colspan="2">ESRF / MASSIF-1</td>
		</tr>
		<tr>
			<td>Wavelength (&#197;)</td>
			<td colspan="2">0.966</td>
		</tr>
		<tr>
			<td>Resolution (&#197;)</td>
			<td>41.88 &#8211; 1.48 (1.53 &#8211; 1.48)</td>
			<td>41.86 - 1.32 (1.39 &#8211; 1.32)</td>
		</tr>
		<tr>
			<td rowspan="2">Total/Unique reflections</td>
			<td>127670 / 28644</td>
			<td>177332 / 40134</td>
		</tr>
		<tr>
			<td>(12178 / 2775)</td>
			<td>(23772 / 5714)</td>
		</tr>
		<tr>
			<td>Space group for indexing, scaling and merging</td>
			<td>C222</td>
			<td>C2221</td>
		</tr>
		<tr>
			<td>Cell dimensions</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>&#160;&#160;&#160;&#160;&#160;&#160; a, b, c (&#197;)</td>
			<td>42.20, 83.75, 95.85</td>
			<td>42.19, 83.72, 95,82</td>
		</tr>
		<tr>
			<td>Mosaicity</td>
			<td>0.05</td>
			<td>0.05</td>
		</tr>
		<tr>
			<td>Rmeas (%)</td>
			<td>10.0 (110.7)</td>
			<td>11.1 (198.2)</td>
		</tr>
		<tr>
			<td>&#60;I/&#963;(I)&#62;</td>
			<td>9.6 (1.3)</td>
			<td>7.6 (0.7)</td>
		</tr>
		<tr>
			<td>CC1/2 (%)</td>
			<td>99.7 (53.9)</td>
			<td>99.7 (19.1)</td>
		</tr>
		<tr>
			<td>Completeness (%)</td>
			<td>99.6 (99.6)</td>
			<td>99.5 (98.6)</td>
		</tr>
		<tr>
			<td>Multiplicity</td>
			<td>4.5 (4.4)</td>
			<td>4.4 (4.2)</td>
		</tr>
		<tr>
			<td colspan="3">Molecular replacement and preliminary model refinement</td>
		</tr>
		<tr>
			<td>Space group for phasing</td>
			<td>C2</td>
			<td>C2221</td>
		</tr>
		<tr>
			<td>Cell dimensions</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>&#160;&#160;&#160;&#160;&#160;&#160; a, b, c (&#197;)</td>
			<td>83.74, 42.18, 95.82</td>
			<td>42.19, 83.72, 95,82</td>
		</tr>
		<tr>
			<td>&#160;&#160;&#160;&#160;&#160;&#160; &#945;, &#946;, &#947; (&#176;)</td>
			<td>90, 90.03, 90</td>
			<td>90, 90, 90</td>
		</tr>
		<tr>
			<td>Search model for MR (PDB)</td>
			<td>3KLR</td>
			<td>3KLR</td>
		</tr>
		<tr>
			<td>Protein molecules / ASU</td>
			<td>2</td>
			<td>1</td>
		</tr>
		<tr>
			<td>Protein residues</td>
			<td>250</td>
			<td>125</td>
		</tr>
		<tr>
			<td>Rwork/Rfree (%) after 1st refinement</td>
			<td>24.3 / 26.5</td>
			<td>20.4 / 23.8</td>
		</tr>
		<tr>
			<td>RMSD bond length (&#197;) after 1st refinement</td>
			<td>0.01</td>
			<td>0.01</td>
		</tr>
		<tr>
			<td>RMSD bond angle (&#176;) after 1st refinement</td>
			<td>1.2</td>
			<td>1.83</td>
		</tr>
		<tr>
			<td>Rotamer outlier (%) after 1st refinement</td>
			<td>1.07</td>
			<td>4.29</td>
		</tr>
		<tr>
			<td>Ramachandran favoured/allowed/disallowed (%) after 1st refinement</td>
			<td>95.93 / 4.07 / 0</td>
			<td>95.12 / 4.88 / 0</td>
		</tr>
	</tbody>
</table>
Table 1: X-ray diffraction data collection, refinement, and validation statistics. Values for the highest resolution shell are given in brackets.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/59032/59032fig1.jpg" /> 
Figure 1: Sample analysis before data collection. (A) The region selected for scanning is shown by a red box. (B) The analysis of diffraction images is shown as a heat map. Four positions within the located crystal were selected for data collection. <a href="https://www-jove-com.bdigitaluss.remotexs.co/files/ftp_upload/59032/59032fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/59032/59032fig2.jpg" /> 
Figure 2: Visual validation of electron density maps obtained after refinement. Electron density maps contoured at 2x r.m.s. level around (a) Trp143, (b) Val66 (Ile in human GCSH), and (c) Glu98 (Asp in human GCSH) and maps contoured at 1x r.m.s level around (d) Phe149 (Leu in human GCSH) and (e) Lys125 (Asp in human GCSH). <a href="https://www-jove-com.bdigitaluss.remotexs.co/files/ftp_upload/59032/59032fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Fully Autonomous Characterization and Data Collection from Crystals of Biological Macromolecules at JoVE.com

Fully Autonomous Characterization and Data Collection from Crystals of Biological Macromolecules

Here, we describe how to use the automated screening and data collection options available at some synchrotron beamlines. Scientists send cryocooled samples to the synchrotron, and the diffraction properties are screened, the data sets are collected and processed and, where possible, a structure solution is carried out&#8212;all without human intervention.

High-brilliance X-ray beams coupled with automation have&#160;led to the use of synchrotron-based macromolecular X-ray crystallography (MX) beamlines for ...

fully-autonomous-characterization-data-collection-from-crystals

Universidad San Sebastian

Research

JoVE Journal

Biochemistry

6.8K Views.  European Synchrotron Radiation Facility. Here, we describe how to use the automated screening and data collection options available at some synchrotron beamlines. Scientists send cryocooled samples to the synchrotron, and the diffraction properties are screened, the data sets are collected and processed and, where possible, a structure solution is carried out—all without human intervention.

Video: Fully Autonomous Characterization and Data Collection from Crystals of Biological Macromolecules

Automated Protocols for Macromolecular Crystallization at the MRC Laboratory of Molecular Biology

When high quality crystals are obtained that diffract X-rays, the crystal structure may be solved at near atomic resolution. The conditions to crystallize proteins, DNAs, RNAs, and their complexes can however not be predicted. Employing a broad variety of conditions is a way to increase the yield of quality diffraction crystals. Two fully automated systems have been developed at the MRC Laboratory of Molecular Biology (Cambridge, England, MRC-LMB) that facilitate crystallization screening against 1,920 initial conditions by vapor diffusion in nanoliter droplets. Semi-automated protocols have also been developed to optimize conditions by changing the concentrations of reagents, the pH, or by introducing additives that potentially enhance properties of the resulting crystals. All the corresponding protocols will be described in detail and briefly discussed. Taken together, they enable convenient and highly efficient macromolecular crystallization in a multi-user facility, while giving the users control over key parameters of their experiments.

Automated systems and protocols for the routine preparation of a large number of screens and nanoliter crystallization droplets for vapor diffusion experiments are described and discussed.

When high quality crystals are obtained that diffract X-rays, the crystal structure may be solved at near atomic resolution. The conditions to crystallize ...

Microcrystallography of Protein Crystals and In Cellulo Diffraction

The advent of high-quality microfocus beamlines at many synchrotron facilities has permitted the routine analysis of crystals smaller than 10 &#181;m in their largest dimension, which used to represent a challenge. We present two alternative workflows for the structure determination of protein microcrystals by X-ray crystallography with a particular focus on crystals grown in vivo. The microcrystals are either extracted from cells by sonication and purified by differential centrifugation, or analyzed in cellulo after cell sorting by flow cytometry of crystal-containing cells. Optionally, purified crystals or crystal-containing cells are soaked in heavy atom solutions for experimental phasing. These samples are then prepared for diffraction experiments in a similar way by application onto a micromesh support and flash cooling in liquid nitrogen. We briefly describe and compare serial diffraction experiments of isolated microcrystals and crystal-containing cells using a microfocus synchrotron beamline to produce datasets suitable for phasing, model building and refinement.
These workflows are exemplified with crystals of the Bombyx mori cypovirus 1 (BmCPV1) polyhedrin produced by infection of insect cells with a recombinant baculovirus. In this case study, in cellulo analysis is more efficient than analysis of purified crystals and yields a structure in ~8 days from expression to refinement.

Microcrystallography of Protein Crystals and In Cellulo Diffraction

A protocol is presented for X-ray crystallography using protein microcrystals. Two examples analyzing in vivo-grown microcrystals after purification or in cellulo are compared.

The advent of high-quality microfocus beamlines at many synchrotron facilities has permitted the routine analysis of crystals smaller than 10 &#181;m in ...

Biochemical and Structural Characterization of the Carbohydrate Transport Substrate-binding-protein SP0092

Development of new antimicrobials and vaccines for Streptococcus pneumoniae (pneumococcus) are necessary to halt the rapid rise in multiple resistant strains. Carbohydrate substrate binding proteins (SBPs) represent viable targets for the development of protein-based vaccines and new antimicrobials because of their extracellular localization and the centrality of carbohydrate import for pneumococcal metabolism, respectively. Described here is a rationalized integrated protocol to carry out a comprehensive characterization of SP0092, which can be extended to other carbohydrate SBPs from the pneumococcus and other bacteria. This procedure can aid the structure-based design of inhibitors for this class of proteins. Presented in the first part of this manuscript are protocols for biochemical analysis by thermal shift assay, multi angle light scattering (MALS), and size exclusion chromatography (SEC), which optimize the stability and homogeneity of the sample directed to crystallization trials and so enhance the probability of success. The second part of this procedure describes the characterization of the SBP crystals using a tunable wavelength anomalous diffraction synchrotron beamline, and data collection protocols for measuring data that can be used to resolve the crystallized protein structure.

A streamlined protocol for performing an extensive biochemical and structural characterization of a carbohydrate substrate binding protein from Streptococcus pneumoniae is presented.

Development of new antimicrobials and vaccines for Streptococcus pneumoniae (pneumococcus) are necessary to halt the rapid rise in multiple resistant ...

An All-in-one Sample Holder for Macromolecular X-ray Crystallography with Minimal Background Scattering

Macromolecular X-ray crystallography (MX) is the most prominent method to obtain high-resolution three-dimensional knowledge of biological macromolecules. A prerequisite for the method is that highly ordered crystalline specimen need to be grown from the macromolecule to be studied, which then need to be prepared for the diffraction experiment. This preparation procedure typically involves removal of the crystal from the solution, in which it was grown, soaking of the crystal in ligand solution or cryo-protectant solution and then immobilizing the crystal on a mount suitable for the experiment. A serious problem for this procedure is that macromolecular crystals are often mechanically unstable and rather fragile. Consequently, the handling of such fragile crystals can easily become a bottleneck in a structure determination attempt. Any mechanical force applied to such delicate crystals may disturb the regular packing of the molecules and may lead to a loss of diffraction power of the crystals. Here, we present a novel all-in-one sample holder, which has been developed in order to minimize the handling steps of crystals and hence to maximize the success rate of the structure determination experiment. The sample holder supports the setup of crystal drops by replacing the commonly used microscope cover slips. Further, it allows in-place crystal manipulation such as ligand soaking, cryo-protection and complex formation without any opening of the crystallization cavity and without crystal handling. Finally, the sample holder has been designed in order to enable the collection of in situ X-ray diffraction data at both, ambient and cryogenic temperature. By using this sample holder, the chances to damage the crystal on its way from crystallization to diffraction data collection are considerably reduced since direct crystal handling is no longer required.

A novel sample holder for macromolecular X-ray crystallography along with a suitable handling protocol is presented. The system allows crystal growth, crystal soaking and in situ diffraction data collection at both, ambient and cryogenic temperature without the need of any crystal manipulation or mounting.

Macromolecular X-ray crystallography (MX) is the most prominent method to obtain high-resolution three-dimensional knowledge of biological macromolecules. ...

Microfluidic Chips for In Situ Crystal X-ray Diffraction and In Situ Dynamic Light Scattering for Serial Crystallography

This protocol describes fabricating microfluidic devices with low X-ray background optimized for goniometer based fixed target serial crystallography. The devices are patterned from epoxy glue using soft lithography and are suitable for in situ X-ray diffraction experiments at room temperature. The sample wells are lidded on both sides with polymeric polyimide foil windows that allow diffraction data collection with low X-ray background. This fabrication method is undemanding and inexpensive. After the sourcing of a SU-8 master wafer, all fabrication can be completed outside of a cleanroom in a typical research lab environment. The chip design and fabrication protocol utilize capillary valving to microfluidically split an aqueous reaction into defined nanoliter sized droplets. This loading mechanism avoids the sample loss from channel dead-volume and can easily be performed manually without using pumps or other equipment for fluid actuation. We describe how isolated nanoliter sized drops of protein solution can be monitored in situ by dynamic light scattering to control protein crystal nucleation and growth. After suitable crystals are grown, complete X-ray diffraction datasets can be collected using goniometer based in situ fixed target serial X-ray crystallography at room temperature. The protocol provides custom scripts to process diffraction datasets using a suite of software tools to solve and refine the protein crystal structure. This approach avoids the artefacts possibly induced during cryo-preservation or manual crystal handling in conventional crystallography experiments. We present and compare three protein structures that were solved using small crystals with dimensions of approximately 10-20 &#181;m grown in chip. By crystallizing and diffracting in situ, handling and hence mechanical disturbances of fragile crystals is minimized. The protocol details how to fabricate a custom X-ray transparent microfluidic chip suitable for in situ serial crystallography. As almost every crystal can be used for diffraction data collection, these microfluidic chips are a very efficient crystal delivery method.

Microfluidic Chips for In Situ Crystal X-ray Diffraction and In Situ Dynamic Light Scattering for Serial Crystallography

This protocol describes in detail how to fabricate and operate microfluidic devices for X-ray diffraction data collection at room temperature. Additionally, it describes how to monitor protein crystallization by dynamic light scattering and how to process and analyze obtained diffraction data.

This protocol describes fabricating microfluidic devices with low X-ray background optimized for goniometer based fixed target serial crystallography. The ...

Chemistry

Workflow and Tools for Crystallographic Fragment Screening at the Helmholtz-Zentrum Berlin

Fragment screening is a technique that helps to identify promising starting points for ligand design. Given that crystals of the target protein are available and display reproducibly high-resolution X-ray diffraction properties, crystallography is among the most preferred methods for fragment screening because of its sensitivity. Additionally, it is the only method providing detailed 3D information of the binding mode of the fragment, which is vital for subsequent rational compound evolution. The routine use of the method depends on the availability of suitable fragment libraries, dedicated means to handle large numbers of samples, state-of-the-art synchrotron beamlines for fast diffraction measurements and largely automated solutions for the analysis of the results.
Here, the complete practical workflow and the included tools on how to conduct crystallographic fragment screening (CFS) at the Helmholtz-Zentrum Berlin (HZB) are presented. Preceding this workflow, crystal soaking conditions as well as data collection strategies are optimized for reproducible crystallographic experiments. Then, typically in a one to two-day procedure, a 96-membered CFS-focused library provided as dried ready-to-use plates is employed to soak 192 crystals, which are then flash-cooled individually. The final diffraction experiments can be performed within one day at the robot-mounting supported beamlines BL14.1 and BL14.2 at the BESSY&#160; II electron storage ring operated by the HZB in Berlin-Adlershof (Germany). Processing of the crystallographic data, refinement of the protein structures, and hit identification is fast and largely automated using specialized software pipelines on dedicated servers, requiring little user input.
Using the CFS workflow at the HZB enables routine screening experiments. It increases the chances for successful identification of fragment hits as starting points to develop more potent binders, useful for pharmacological or biochemical applications.

Crystallographic fragment screening at the Helmholtz-Zentrum Berlin is performed using a workflow with dedicated compound libraries, crystal handling tools, fast data collection facilities&#160;and largely automated data analysis. The presented protocol intends to maximize the output of such experiments to provide promising starting points for downstream structure-based ligand design.

Fragment screening is a technique that helps to identify promising starting points for ligand design. Given that crystals of the target protein are ...

The Automated Crystallography Pipelines at the EMBL HTX Facility in Grenoble

EMBL Grenoble operates the High Throughput Crystallization Laboratory (HTX Lab), a large-scale user facility offering high throughput crystallography services to users worldwide. The HTX lab has a strong focus in the development of new methods in macromolecular crystallography. Through the combination of a high throughput crystallization platform, the CrystalDirect technology for fully automated crystal mounting and cryocooling and the CRIMS software we have developed fully automated pipelines for macromolecular crystallography that can be remotely operated over the internet. These include a protein-to-structure pipeline for the determination of new structures, a pipeline for the rapid characterization of protein-ligand complexes in support of medicinal chemistry, and a large-scale, automated fragment screening pipeline enabling evaluation of libraries of over 1000 fragments. Here we describe how to access and use these resources.

Here, we describe how to use the automated macromolecular crystallography pipelines for protein-to-structure, rapid ligand-protein complex analysis and large-scale fragment screening based on the CrystalDirect technology at the HTX Laboratory in EMBL Grenoble.

EMBL Grenoble operates the High Throughput Crystallization Laboratory (HTX Lab), a large-scale user facility offering high throughput crystallography ...

Crystallization of Proteins on Chip by Microdialysis for In Situ X-ray Diffraction Studies

This protocol describes the manufacturing of reproducible and inexpensive microfluidic devices covering the whole pipeline for crystallizing proteins on-chip with the dialysis method and allowing in situ single-crystal or serial crystallography experiments at room temperature. The protocol details the fabrication process of the microchips, the manipulation of the on-chip crystallization experiments and the treatment of the in situ collected X-ray diffraction data for the structural elucidation of the protein sample. The main feature of this microfabrication procedure lies on the integration of a commercially available, semipermeable regenerated cellulose dialysis membrane in between two layers of the chip. The molecular weight cut-off of the embedded membrane varies depending on the molecular weight of the macromolecule and the precipitants. The device exploits the advantages of microfluidic technology, such as the use of minute volumes of samples (&#60;1 &#181;L) and fine tuning over transport phenomena. The chip coupled them with the dialysis method, providing precise and reversible control over the crystallization process and can be used for investigating phase diagrams of proteins at the microliter scale. The device is patterned using a photocurable thiolene-based resin with soft imprint lithography on an optically transparent polymeric substrate. Moreover, the background scattering of the materials composing the microchips and generating background noise was evaluated rendering the chip compatible for in situ X-ray diffraction experiments. Once protein crystals are grown on-chip up to an adequate size and population uniformity, the microchips can be directly mounted in front of the X-ray beam with the aid of a 3D printed holder. This approach addresses the challenges rising from the use of cryoprotectants and manual harvesting in conventional protein crystallography experiments through an easy and inexpensive manner. Complete X-ray diffraction data sets from multiple, isomorphous lysozyme crystals grown on-chip were collected at room temperature for structure determination.

Crystallization of Proteins on Chip by Microdialysis for In Situ X-ray Diffraction Studies

This paper details the fabrication protocol of microfluidic chips developed for on-chip protein crystallization with the dialysis method and in situ X-ray diffraction experiments. The microfabrication process makes it possible to integrate a semipermeable regenerated cellulose dialysis membrane with any molecular weight cut-off, between two layers of the chip.

This protocol describes the manufacturing of reproducible and inexpensive microfluidic devices covering the whole pipeline for crystallizing proteins ...

On-Chip Crystallization and Large-Scale Serial Diffraction at Room Temperature

Biochemical reactions and biological processes can be best understood by demonstrating how proteins transition among their functional states. Since cryogenic temperatures are non-physiological and may prevent, deter, or even alter protein structural dynamics, a robust method for routine X-ray diffraction experiments at room temperature is highly desirable. The crystal-on-crystal device and its accompanying hardware and software used in this protocol are designed to enable in situ X-ray diffraction at room temperature for protein crystals of different sizes without any sample manipulation. Here we present the protocols for the key steps from device assembly, on-chip crystallization, optical scanning, crystal recognition to X-ray shot planning and automated data collection. Since this platform requires no crystal harvesting nor any other sample manipulation, hundreds to thousands of protein crystals grown on chip can be introduced into an X-ray beam in a programmable and high-throughput manner.

This contribution describes how to set up protein crystallization on crystal-on-crystal devices and how to perform automated serial data collection at room temperature using the on-chip crystallization platform.

Biochemical reactions and biological processes can be best understood by demonstrating how proteins transition among their functional states. Since ...

Automated Protein Crystallization and Real-Time Data Collection

Crystallization and In Situ Room Temperature Data Collection Using the Crystallization Facility at Harwell and Beamline VMXi, Diamond Light Source

Protocols for robotic protein crystallization using the Crystallization Facility at Harwell and in situ room temperature data collection from crystallization plates at Diamond Light Source beamline VMXi are described. This approach enables high-quality room-temperature crystal structures to be determined from multiple crystals in a straightforward manner and provides very rapid feedback on the results of crystallization trials as well as enabling serial crystallography. The value of room temperature structures in understanding protein structure, ligand binding, and dynamics is becoming increasingly recognized in the structural biology community. This pipeline is accessible to users from all over the world with several available modes of access. Crystallization experiments that are set up can be imaged and viewed remotely with crystals identified automatically using a machine learning tool. Data are measured in a queue-based system with up to 60&#176; rotation datasets from user-selected crystals in a plate. Data from all the crystals within a particular well or sample group are automatically merged using xia2.multiplex with the outputs straightforwardly accessed via a web browser interface.

Author Spotlight: Advancing Protein Structure Analysis for Drug Development 

We present a protocol for the crystallization of proteins using the crystallization facility in the Research Complex at Harwell and subsequent in situ X-ray crystallographic data collection from crystals within the plates at Diamond&#39;s Versatile Macromolecular Crystallography in situ (VMXi) beamline. We describe sample requirements, crystallization protocols, and data collection guidelines.

Fully Autonomous Characterization and Data Collection from Crystals of Biological Macromolecules

Summary

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Chapters in this video

Automated Protocols for Macromolecular Crystallization at the MRC Laboratory of Molecular Biology

Microcrystallography of Protein Crystals and In Cellulo Diffraction

Biochemical and Structural Characterization of the Carbohydrate Transport Substrate-binding-protein SP0092

An All-in-one Sample Holder for Macromolecular X-ray Crystallography with Minimal Background Scattering

Microfluidic Chips for In Situ Crystal X-ray Diffraction and In Situ Dynamic Light Scattering for Serial Crystallography

Workflow and Tools for Crystallographic Fragment Screening at the Helmholtz-Zentrum Berlin

The Automated Crystallography Pipelines at the EMBL HTX Facility in Grenoble

Crystallization of Proteins on Chip by Microdialysis for In Situ X-ray Diffraction Studies

On-Chip Crystallization and Large-Scale Serial Diffraction at Room Temperature

Crystallization and In Situ Room Temperature Data Collection Using the Crystallization Facility at Harwell and Beamline VMXi, Diamond Light Source