Name: utilizing phluorin-tagged receptors to monitor subcellular localization and trafficking
Uploaded: 2017-03-16T14:00:00.000+00:00
Duration: 9 min 59 s
Description: Watch this Scientific Journal Video about Utilizing pHluorin-tagged Receptors to Monitor Subcellular Localization and Trafficking at JoVE.com

This work was supported in part by the National Institute on Drug Abuse T32 DA 016176, National Institute on Drug Abuse DA 038817, and National Institute on Drug Abuse DA 040047.

1. Cell Culture and Transfection
<ol>
	<li>Maintain mouse neuroblastoma 2a (N2a) cells in growth media.
	<ol>
		<li>Make 500 ml N2a growth media from 200 ml Dulbecco&#39;s Eagle medium (DMEM) with high glucose, 250 ml reduced serum media, 50 ml fetal bovine serum (FBS), and 5 ml penicillin/streptomycin (100x).</li>
		<li>Maintain cells in a T75 flask at 37 &#176;C in a 5% CO2 incubator.</li>
		<li>Split cells 1:15 when necessary, or at approximately 80-90% confluency. This is typically 2-3 times a week.</li>
	</ol>
	</li>
	<li>Coat 35 mm glass bottom dish with poly-D-lysine.
	<ol>
		<li>In a laminar flow biosafety cabinet, add 200 &#181;l of 0.1 &#181;g/ml poly-D-lysine onto glass bottom region of sterile 35 mm dish.</li>
		<li>Place dish in a 37 &#176;C incubator for 1 hr.</li>
		<li>Carefully rinse dish with ddH2O 3-4 times.</li>
		<li>Allow dishes to completely dry for more than 1 hr.</li>
		<li>Sterilize dishes using UV light in the biosafety cabinet if necessary.</li>
	</ol>
	</li>
	<li>Plate N2a cells for TIRFM imaging.
	<ol>
		<li>Remove growth media from adherent cells.</li>
		<li>Detach cells from the flask by incubating with 1 ml 1x trypsin (+EDTA) for 5 min at 37 &#176;C in a 5% CO2 incubator.</li>
		<li>Inactivate trypsin by adding 9 ml growth media. Mix media, trypsin, and detached cells using a pipette.</li>
		<li>Visually count cells using a hemocytometer and calculate the correct volume to add 90,000 cells to each poly-D-lysine coated glass bottom dish. This density is required for efficient transfection and single cell TIRF imaging.</li>
		<li>Add 2 ml growth media to each glass-bottom dish containing 90,000 cells.</li>
		<li>Incubate the dish at 37 &#176;C in a 5% CO2 incubator for 16-24 hr.</li>
	</ol>
	</li>
	<li>N2a transfection
	<ol>
		<li>Obtain a plasmid construct containing an SEP fluorophore incorporated into the extracellular region of the protein of interest. Standard cloning techniques such as PCR amplification5 can be used to generate the construct. 
		NOTE: SEP should be incorporated into the extracellular region of the membrane protein so that it resides within the lumen of the endoplasmic reticulum or trafficking vesicles and is exposed to extracellular solution when on the plasma membrane. SEP is similar in size to GFP and similar cloning strategies can be used.</li>
		<li>Replace the growth media on plated cells with 1.5 ml reduced serum media (e.g., Opti-MEM), approximately 30 min before the addition of the transfection reagent. 
		NOTE: To study drug induced changes in receptors, an appropriate concentration of drug can be added at the time of the transfection.</li>
		<li>Add 500 ng of each desired plasmid construct to 250 &#181;l reduced serum media (tube 1).</li>
		<li>Add 2 &#181;l of the transfection reagent to a separate tube containing 250 &#181;l of reduced serum media. Incubate tube 2 at room temperature for 5 min. The ratio of transfection reagent to plasmid DNA should be optimized to express each protein of interest.</li>
		<li>Combine tubes 1 and 2 to make a solution containing 500 &#181;l of transfection reagent and plasmid mix. Incubate at room temperature for 25 min.</li>
		<li>Add the 500 &#181;l transfection mix to pre-plated cells for a total volume of 2 ml per dish.</li>
		<li>Incubate cells at 37 &#176;C in a 5% CO2 incubator for 24 hr.</li>
		<li>After 24 hr, remove the transfection mix and rinse the cells with growth media and then add 2 ml of growth media to each dish. 
		NOTE: If a drug was added at the time of transfection, it can be replenished again at this step.</li>
		<li>Incubate cells at 37 &#176;C in a 5% CO2 incubator for 24 hr.</li>
		<li>Image cells 48 hr after transfection.</li>
	</ol>
	</li>
</ol>
2. Live Cell Imaging by Total Internal Reflection Fluorescence Microscopy (TIRFM)
<ol>
	<li>Imaging set up
	<ol>
		<li>Perform imaging with an inverted fluorescence microscope set-up with a scanning stage as shown in Figure 1. This requires alignment of a 488 nm DPSS laser source, a stepper motor to adjust 488 nm beam position, and a high numerical aperture (1.49 NA) 60X or 100X oil immersion objective.</li>
		<li>Pass the laser beam through the appropriate excitation filter (bandpass 488/10 nm). Align the polarized laser beam through a single mode fiber connected to a launcher mounted to a stepper motor. In epifluorescence mode, the excitation beam is centered in the middle of the back aperture of the objective.</li>
		<li>To attain TIRF, use the stepper motor to translate the focused laser beam across the back aperture of the objective lens until the critical angle is reached and beam is no longer transmitted through the sample and is instead totally reflected off the glass-cell interface.</li>
		<li>Capture images using an EMCCD (512 x 512 pixels) controlled with imaging software (e.g. Metamorph) with the appropriate emission filter mounted in the emission pathway (525/50 nm).</li>
	</ol>
	</li>
	<li>Prepare the imaging solution
	<ol>
		<li>Prepare 200 ml extracellular solution (ECS) by mixing 150 mM NaCl, 4 mM KCl, 2 mM MgCl2, 2 mM CaCl2, 10 mM HEPES and 10 mM glucose in ddH2O. Stock solutions of NaCl, KCl, MgCl2, and CaCl2 can be prepared in advance and combined with fresh HEPES and glucose on the day of imaging.</li>
		<li>Adjust the pH of a solution containing 100 ml ECS to pH 7.4. Adjust the remaining 100 ml of ECS to a pH of 5.4. Rinse the transfected cells with 2 ml of ECS (pH 7.4).</li>
		<li>Add 2 ml of ECS (pH 7.4) to the transfected cells before imaging.</li>
	</ol>
	</li>
	<li>Live cell imaging in TIRF
	<ol>
		<li>Turn on the entire system, including 488 nm laser, camera, translation stage, and imaging program. Focus the epifluorescence beam and adjust the power to approximately 1 mW at the 60X objective.</li>
		<li>Add oil to the objective and place a dish of transfected cells on the translation stage. Secure the dish in place using stage mounts to ensure it does not move with respect to the stage so the cells can be imaged multiple times.</li>
		<li>In epifluorescence mode, focus the microscope and locate the fluorescent, transfected cells. Cells will remain focused across several focus planes. Locate single, isolated cells to proceed with TIRF.</li>
		<li>In the imaging program, set the exposure time to 200 msec and optimize the fluorescence intensity by setting the EM gain.</li>
		<li>Transition the laser beam into TIRF by translating the beam across the objective in a stepwise manner using the stepper motor. As the critical angle approaches, the beam will visibly translate across the edge of the dish until it converges at the point of total internal reflection on the sample plane.</li>
		<li>Verify that cells are in TIRF mode by adjusting the focus knob. In TIRF, only one plane of cells can be focused (i.e. approximately 150 nm from glass interface), producing a very defined image with high resolution of the plasma membrane.</li>
	</ol>
	</li>
	<li>Imaging SEP to determine subcellular localization
	<ol>
		<li>Locate healthy, transfected, single cells in the imaging plane.</li>
		<li>Acquire a focused image of cell at pH 7.4. SEP labeled receptors on the plasma membrane and endoplasmic reticulum should be visible.</li>
		<li>Quickly block the laser beam from reaching the sample to prevent photobleaching.</li>
		<li>Memorize the stage positions corresponding to each cell using microscope imaging software capable of recording multiple xy locations.</li>
		<li>Repeat steps 2.4.1-2.4.4 for 20-30 cells per dish while using the software to record the position of each cell.</li>
		<li>After all the cell images at pH 7.4 are collected, manually remove the pH 7.4 ECS solution using a pipette. Do not touch the dish as this could move the memorized stage positions.</li>
		<li>Carefully add 2 ml of pH 5.4 ECS to the dish and wait 10 min. During this time, save previously acquired images.</li>
		<li>Under the identical set of conditions used to collect images at pH 7.4, move the stage to each saved position and acquire an image of the same cell at pH 5.4. Cells should look less defined since all detected fluorescence is originating from endoplasmic reticulum confined SEP labeled receptors. Save the pH 5.4 cell images.</li>
	</ol>
	</li>
	<li>Imaging single vesicle insertion events in live cells
	<ol>
		<li>Replace growth media of transfected cells with 2 ml pH 7.4 ECS, or with Leibovitz&#39;s L-15 media. The pH of Leibovitz&#39;s L-15 media is CO2 independent, allowing imaging to take place over a long period of time if necessary.</li>
		<li>Place the dish of transfected cells on the stage of the microscope. Secure and focus a single cell in TIRF following Step 2.3 above.</li>
		<li>If equipped, set the autofocus so the focus does not drift over the period of imaging.</li>
		<li>Record a series of 1,000 frames, continuously capturing images at a frame rate of 200 msec. Bursts of fluorescence will be visible during this time, corresponding to low pH trafficking vesicles fusing with the plasma membrane, exposing the SEP to the extracellular pH 7.4.</li>
		<li>Locate another single cell and repeat the above step. Reset autofocus if necessary.</li>
	</ol>
	</li>
</ol>
3. Image Analysis and Data Processing
<ol>
	<li>Analyzing SEP fluorescence to determine subcellular localization
	<ol>
		<li>Open the cell images using an image analysis software such as Metamorph or ImageJ (http://imagej.nih.gov/ij/). Subtract the background from both pH 5.4 and pH 7.4 images using the rolling ball setting.</li>
		<li>Use an intensity based threshold to quantify fluorescence from a single cell. Manually select a region of interest around the cell in the pH 7.4 image.</li>
		<li>Measure the cell area, mean intensity, and integrated density using a plugin in ImageJ or using the built in &#34;Measure&#34; function under the Analyze tab.</li>
		<li>Repeat steps 3.1.1-3.1.3 for the same cell at pH 5.4, carefully adjusting the intensity based threshold and region of interest in the same manner.</li>
		<li>After the integrated density is obtained for cell images at both pH 7.4 and 5.4, calculate the plasma membrane integrated density by subtracting the pH 5.4 value from the pH 7.4 value. The difference corresponds to the relative number receptors on the plasma membrane within the TIRF excitation region.</li>
		<li>As a measure of trafficking, calculate the relative percentage of SEP labeled receptors located on the plasma membrane compared to the remaining receptors visible in the TIRF excitation volume by dividing the plasma membrane integrated density by the total integrated density at pH 7.4, multiplied by 100.</li>
	</ol>
	</li>
	<li>Analyzing single vesicle insertion events
	<ol>
		<li>Open the series of 1,000 tiff images using image analysis software. Subtract the background from all frames using the rolling ball setting.</li>
		<li>Adjust the color balance of the recording to maximize intense regions corresponding to vesicle insertion events. Manually count the bursts of fluorescence lasting longer than 3 frames (&#62;600 msec).</li>
	</ol>
	</li>
</ol>

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The authors have no conflicts of interest to declare.

The pH sensitivity of SEP enables receptors residing on the plasma membrane to be distinguished from intracellular receptors in the endoplasmic reticulum, and it can be used to resolve insertion events of receptor-carrying vesicles5,7,8,9,18,19,20. Several techniques including surface biotinylation and ligand binding are widely used to measure protein surface levels. In some cases, western blots can also be used to distinguish between ER and PM resident protein. This SEP-based technique is complementary to traditional measurements, providing a rapid readout of surface expression and the ability to quantify shifts in protein localized on the ER to the PM. Since SEP is genetically encoded in the protein of interest, issues with nonspecific binding are eliminated and sensitivity is increased. SEP undergoes 488 nm excitation at neutral pH, but is not excited under acidic conditions of pH &#60;6. When the extracellular pH is 7.4, fluorescence is measured for nAChRs residing in the endoplasmic reticulum and on the plasma membrane, but not for those in the lower pH secretory vesicles or Golgi (pH &#60; 6)23. During imaging, the ECS of pH 7.4 is exchanged for an otherwise identical solution at pH 5.4. The difference between the integrated density in these images is the plasma membrane integrated density of a cell. Dividing this number by the total integrated density within the region of TIRF excitation, at pH 7.4, multiplied by 100, gives the percentage on the plasma membrane5,7,8,9. While these studies used TIRFM, similar assays can be performed using epi-fluorescence. For membrane receptors like nAChR where a majority of receptors reside in the ER, TIRM is ideal because the narrow excitation volume increases the fraction of visible PM resident receptors versus intracellular receptors. This increases the sensitivity of the assay to shifts in receptor distribution between organelles. For proteins with higher expression levels on the PM, epi-fluorescence based SEP studies are sufficient to measure changes in receptor expression. However, single vesicle insertion events which are also measured at pH 7.4 require TIRFM. The burst of fluorescence corresponding to the low pH trafficking vesicle fusing with the higher pH plasma membrane while readily seen in TIRFM is typically not discernable in epi-fluorescence.
Incorporating SEP with TIRF Imaging Conditions
SEP can be genetically incorporated into the extracellular domain of a membrane protein. Due to the size and location of SEP, it is critical to verify that the modified protein does not significantly differ in trafficking or function from a wild type protein. Assays should be performed using the SEP labeled protein to verify that incorporation of the label did not disrupt activity. For ion channels, electrophysiology and ion permeability measurements are ideal, while for other receptors fluorescent ligand binding and western blotting can be used to verify trafficking. Adherent cells are ideally suited for transfection with commercial transfection reagents and imaging with TIRFM because they attach directly to the glass bottom dish. This attachment is necessary to ensure TIRF excitation by the evanescent wave within about 150 nm from the glass-sample interface. To achieve high resolution TIRF images, the sample needs to remain flat during imaging21. Poly-D-lysine coating is beneficial when imaging N2a cells because it provides an attachment matrix that minimizes cell movements to maintain a flat surface7. The plating cell density needs to be optimized to ensure cells are isolated on the glass dish to achieve TIRF. Cell clustering impedes total internal reflection by preventing flat cell adherence in a single optical plane. Since only one plane is focused in TIRF, maintaining proper cell morphology is crucial for imaging. This is particularly important when solutions are being exchanged in the SEP studies. To minimize morphological changes, images at pH 7.4 and pH 5.4 need to be collected quickly. In addition, the ECS (pH 5.4) will eventually permeate intracellular membranes, altering organelle structure and fluorescence of internal SEP-labeled receptors. This is easily avoided by collecting images under each pH condition within a few minutes. Data from multiple dishes in the same imaging session can be combined to increase the number of cells analyzed. When changing solutions, carefully remove the pH 7.4 ECS solution with a pipette and add pH 5.4 ECS dropwise into the dish. Removing or adding solution too quickly can stress the cells or move the dish with respect to the saved stage positions. A perfusion system to exchange solutions can also be utilized, as long as the solution exchange is complete and occurs quickly. Exact salt concentrations in each solution are required to minimize cell distortions. A stage top incubator can be incorporated to reduce fluctuations in temperature while imaging.
TIRF Imaging
TIRF imaging reduces background fluorescence by focusing on a single optical plane. This increases the signal to noise ratio by selectively exciting fluorophores within approximately 150 nm from the glass-sample interface21,22. Within this region, resolution is greatly increased, particularly at the plasma membrane. This is necessary if a majority of receptors are located intracellularly. If a high fraction of membrane receptors is located on the plasma membrane, this SEP based approach can be utilized to determine subcellular localization in epifluorescence. However, if a small percentage of total receptors are trafficked to the plasma membrane, as with nAChRs, TIRFM is necessary to quantify pH dependent changes in fluorescence at the plasma membrane. Also, TIRFM allows the resolution of single vesicle trafficking events and distribution of receptors within the secretory pathway. A basic TIRF setup employs a 488 nm DPSS laser for SEP excitation, fiber coupled to a stepper motor to adjust the critical angle of the excitation beam. To achieve TIR, the beam is translated laterally across the back aperture of the objective until a critical angle is reached. Cells are imaged using a 60X or 100X, 1.49 NA oil immersion objective. A numerical aperture higher than the refractive index of the sample (&#62;1.38 for cells) is required to reach the critical angle required for TIRF. A 1.45 NA objective would suffice, but 1.49 NA is more practical when manipulating the angle of excitation. Emission is detected using an electron-multiplying charge coupled device (EMCCD) with an 8 mm array of 512 x 512 pixels. Using a 60X objective, multiple isolated cells can be captured within one field of view.
One of the major drawbacks to fluorescence based studies of protein expression is photobleaching15. This excitation induced decomposition of the fluorophore results in an irreversible decrease in fluorescence intensity over time. For this reason, successful imaging relies on a delicate balance between the intensity of the beam of excitation and on-chip gain used within the EMCCD. The excitation intensity needs to be high enough to excite a fluorophore for detection, but not so high as to photobleach the molecule rapidly. Camera gain can be used to multiply the signal for detection, as opposed to increasing excitation intensity, but this also increases background intensity. In addition, care must be taken when choosing the EM gain settings, to avoid saturation of the images. In between measurements, blocking the excitation beam before it reaches the sample minimizes photobleaching. This is required when collecting cell images at an ECS of pH 7.4 to compare to pH 5.4. Photobleaching occurring between the two images is indistinguishable from a lack of fluorescence due to pH change, so this effect needs to be minimized. Care should be taken to use low laser power and to expose the cell only for the duration necessary to capture the required images. For each experiment, a set of cells can be measured at pH 7 under identical imaging conditions as a control. Using no interval and exposing for a duration matching the exposure time needed for performing the assay provides a control to determine the extent of photobleaching. If photobleaching is greater than 10% of the original intensity, a correction curve can be used from the observed photobleaching rate by collecting a time trace of fluorescence intensity. For single vesicle insertion events, SEP-labeled receptors in trafficking vesicles are not excited until fusion with the plasma membrane, either because the pH dictates an off state or they are outside the TIRF region of excitation. Therefore, SEP tagged receptors will not photobleach until insertion, allowing higher excitation power to be used in order to detect single SEP molecules.
In conclusion, this technique can be used with a variety of adherent cell types. SEP can be incorporated into virtually any membrane protein, as long as protein function and trafficking properties are maintained. TIRF enhances the resolution at the plasma membrane. SEP allows the differentiation of tagged proteins located on the plasma membrane from those within the peripheral endoplasmic reticulum.

Changes in receptor expression, distribution, and assembly have been connected to a wide variety of diseases, including Alzheimer&#39;s disease, Parkinson&#39;s disease, cystic fibrosis, and drug addiction1,2,3,4,5. For example, nicotine and other nicotinic ligands influence the trafficking of nicotinic acetylcholine receptors (nAChRs) leading to changes in trafficking, expression, and upregulation1,2,5,6,7,8,9,10. Nicotine increases the total number of assembled nAChRs within a cell, increases trafficking towards the plasma membrane, and alters the assembly of subunits to favor a high sensitivity version of some subtypes. Resolving distinct changes in trafficking, assembly, and expression of receptors in a disease model provides crucial mechanistic details that are essential to define drug targets. An ideal approach would rapidly differentiate between intracellular receptors and those localized on the plasma membrane. This is particularly challenging in cases where a majority of a particular protein resides intracellularly, such as with nAChRs. Since the majority of nAChRs are localized to the endoplasmic reticulum, traditional measurements lack the spatio-temporal resolution necessary to pinpoint localization and trafficking changes along the secretory pathway. Receptor trafficking and expression studies of nAChRs have primarily been conducted using radioligand binding11, biotinylation assays12, western blotting13, or immunoprecipitation techniques12. These depend on the binding specificity of a reporter molecule or fixation of cells and lack the ability to simultaneously distinguish between plasma membrane resident and intracellular receptors. Therefore, studies of ion channel assembly and vesicle dynamics have largely relied on low-throughput electrophysiological techniques14.
Superior spatial and temporal resolution is possible with advances in fluorescence microscopy. Genetically encoded reporter molecules, such as green fluorescent protein (GFP) and its variants, eliminate nonspecific binding issues and increase sensitivity15. A pH sensitive variant of GFP, known as superecliptic pHluorin (SEP), can be used to exploit inherent pH differences between compartments within a cell to determine localization5,7,8,9,16,17,18. SEP fluoresces when the pH is higher than 6, but remains in an off state at lower pH. Therefore, receptors tagged with SEP on their luminal side are detected when present in the endoplasmic reticulum (ER) or upon insertion into the plasma membrane (PM), but not when confined to a trafficking vesicle. Manipulation of the extracellular pH in contact with receptors on the plasma membrane consequently alters the fluorescence and therefore detection of these receptors. If the same cell is sequentially imaged at both a neutral extracellular pH and then a pH lower than 6, the difference between the images is attributed to receptors located on the plasma membrane. This allows a simultaneous measurement of intracellular (peripheral ER) and plasma membrane resident receptors5,7,8,9. Single vesicle insertion events can also be resolved when the extracellular pH is neutral. Once a low pH trafficking vesicle fuses with the plasma membrane, the luminal side of the vesicle is exposed to the neutral extracellular solution, causing a transition detected as a burst of fluorescence7,18,19,20. SEP enables the measurement of receptors localized to the plasma membrane and peripheral endoplasmic reticulum, and provides a means to measure trafficking of receptors between these subcellular regions5,7,18.
To achieve higher resolution at the plasma membrane, a receptor with SEP genetically encoded is imaged by total internal reflection florescence microscopy (TIRFM). This method is particularly useful if the majority of receptors are localized to intracellular regions, since TIRFM increases the visibility of the plasma membrane. TIRFM also enables the resolution of trafficking dynamics of single vesicles carrying SEP-labeled receptors upon insertion into the PM. Total internal reflection occurs at the interface of materials with different refractive indices, such as between a cell and a glass cover-slip21,22. SEP fluoresces when irradiated with 488 nm excitation, which is oriented to achieve total internal reflection at the interface of the glass and cell solution. This produces an evanescent wave that penetrates approximately 150 nm into the sample, only exciting fluorophores within this volume. Only SEP containing receptors in a neutral pH environment within this range of excitation are detected, corresponding to those residing on the plasma membrane or peripheral endoplasmic reticulum. Since detection is limited to excitation by the evanescent wave, background fluorescence from the intracellular region is reduced and the signal to noise ratio is increased21,22. In addition, since radiation does not penetrate the bulk of the cell, photodamage is minimized which allows live cell imaging over the course of time. As a result, TIRFM coupled with genetically encoded SEP provides the high resolution and sensitivity required to measure subcellular localization and trafficking dynamics of membrane receptors along the secretory pathway.

<table><tbody><tr><td>&lt;strong&gt;Reagent/Material&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Cell Culture Flasks with Filter Cap, Sterile, Greiner Bio One, 75 cm&lt;sup&gt;2&lt;/sup&gt;</td><td>VWR</td><td>82050-856</td><td></td></tr><tr><td>35 mm glass bottom Petri dishes, sterile</td><td>Cell E&amp;amp;G</td><td>GBD00002-200</td><td></td></tr><tr><td>Poly-D-lysine</td><td>vwr</td><td>215017510</td><td></td></tr><tr><td>Dulbecco Modified Eagle Medium&amp;lrm; (DMEM), High Glucose</td><td>Fisher Scientific</td><td>11-965-084&amp;nbsp;</td><td></td></tr><tr><td>Opti-MEM I Reduced Serum Medium</td><td>Gibco / Fisher Scientific</td><td>31-985-088</td><td></td></tr><tr><td>Fetal Bovine Serum, Certified, US Origin, Standard (Sterile-Filtered)&amp;nbsp;</td><td>Gibco / Fisher Scientific</td><td>16-000-044</td><td></td></tr><tr><td>TrypLE Express Enzyme (1x), no phenol red</td><td>Fisher Scientific</td><td>12604-021</td><td></td></tr><tr><td>Penicillin-Streptomycin Solution</td><td>VWR</td><td>45000-652</td><td></td></tr><tr><td>Leibovitz&#039;s L-15 Medium, no phenol red</td><td>Gibco / Fisher Scientific</td><td>21083027</td><td>Optional</td></tr><tr><td>Lipofectamine</td><td>Fisher Scientific</td><td>11668030</td><td>Gently mix; Do not vortex</td></tr><tr><td>Sodium chloride</td><td>Fisher Scientific</td><td>BP358-1</td><td></td></tr><tr><td>Potassium chloride</td><td>Fisher Scientific</td><td>P217-10</td><td></td></tr><tr><td>Magnesium chloride</td><td>Fisher Scientific</td><td>BP214-500</td><td></td></tr><tr><td>Calcium chloride</td><td>Fisher Scientific</td><td>C79-500</td><td></td></tr><tr><td>HEPES</td><td>Fisher Scientific</td><td>BP310-500</td><td></td></tr><tr><td>D-Glucose</td><td>Fisher Scientific</td><td>D16-1</td><td></td></tr><tr><td>Objective immersion oil&amp;nbsp;</td><td>Olympus</td><td>Type F</td><td></td></tr><tr><td>&lt;strong&gt;Name&lt;/strong&gt;</td><td>&lt;strong&gt;Company&lt;/strong&gt;</td><td>&lt;strong&gt;Catalog Number&lt;/strong&gt;</td><td>&lt;strong&gt;Comments&lt;/strong&gt;</td></tr><tr><td>&lt;strong&gt;Equipment&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Microscope</td><td>Olympus</td><td>IX81</td><td></td></tr><tr><td>Camera</td><td>Andor</td><td>iXon Ultra 897</td><td></td></tr><tr><td>60X, 1.49 NA oil immersion objective</td><td>Olympus</td><td>APON 60XOTIRF</td><td></td></tr><tr><td>Motorized stage</td><td>Prior</td><td>IXPROXY</td><td></td></tr><tr><td>Motorized actuator (stepper motor)</td><td>Thorlabs</td><td>ZST213</td><td></td></tr><tr><td>MetaMorph (or other imaging program)</td><td>Metamorph</td><td></td><td></td></tr><tr><td>488 nm laser</td><td>Market Tech</td><td></td><td></td></tr><tr><td>Single mode fiber</td><td>Thorlabs</td><td>SM450</td><td></td></tr><tr><td>Mirrors</td><td>Thorlabs</td><td>BB1-E01</td><td></td></tr><tr><td>Dichroic 488 nm LP</td><td>Semrock</td><td>Di02-R488-25x36</td><td></td></tr><tr><td>Bandpass filter, 488 nm</td><td>Semrock</td><td>LL01-488-12.5</td><td></td></tr><tr><td>Bandpass filter, 525/50</td><td>Semrock</td><td>FF03-525/50-25</td><td></td></tr></tbody></table>

utilizing phluorin-tagged receptors to monitor subcellular localization and trafficking

Understanding membrane protein trafficking, assembly, and expression requires an approach that differentiates between those residing in intracellular organelles and those localized on the plasma membrane. Traditional fluorescence-based measurements lack the capability to distinguish membrane proteins residing in different organelles. Cutting edge methodologies transcend traditional methods by coupling pH-sensitive fluorophores with total internal reflection fluorescence microscopy (TIRFM). TIRF illumination excites the sample up to approximately 150 nm from the glass-sample interface, thus decreasing background, increasing the signal to noise ratio, and enhancing resolution. The excitation volume in TIRFM encompasses the plasma membrane and nearby organelles such as the peripheral ER. Superecliptic pHluorin (SEP) is a pH sensitive version of GFP. Genetically encoding SEP into the extracellular domain of a membrane protein of interest positions the fluorophore on the luminal side of the ER and in the extracellular region of the cell. SEP is fluorescent when the pH is greater than 6, but remains in an off state at lower pH values. Therefore, receptors tagged with SEP fluoresce when residing in the endoplasmic reticulum (ER) or upon insertion in the plasma membrane (PM) but not when confined to a trafficking vesicle or other organelles such as the Golgi. The extracellular pH can be adjusted to dictate the fluorescence of receptors on the plasma membrane. The difference in fluorescence between TIRF images at neutral and acidic extracellular pH for the same cell corresponds to a relative number of receptors on the plasma membrane. This allows a simultaneous measurement of intracellular and plasma membrane resident receptors. Single vesicle insertion events can also be measured when the extracellular pH is neutral, corresponding to a low pH trafficking vesicle fusing with the plasma membrane and transitioning into a fluorescent state. This versatile technique can be exploited to study localization, expression, and trafficking of membrane proteins.

SEP incorporation into a receptor allows direct detection of that receptor in a live cell. Coupled with TIRFM, this allows the evaluation of the relative expression levels on the plasma membrane and the distribution of receptors within the subcellular locations in the region of TIRF excitation. Single vesicle trafficking events can also be resolved.
Relative Expression Levels of SEP-labeled Receptors on Plasma Membrane
SEP fluorescence upon excitation is dictated by the pH of the surrounding solution. When SEP is fused with plasma membrane resident receptors, the extracellular pH can be manipulated to turn this fluorescence on or off5,7,8,9,17. When the pH of the extracellular solution is a physiological 7.4, receptors from both the plasma membrane and the endoplasmic reticulum within the region of TIRF excitation fluoresce. The extracellular solution can then be exchanged with an otherwise identical solution of pH 5.4. This causes the plasma membrane resident SEP to transition into an off state, meaning all observed fluorescence is now from the endoplasmic reticulum. Figure 2 shows an example of cells imaged at both pH 7.4 (A) and pH 5.4 (B). The relative number of receptors on the plasma membrane compared to the peripheral endoplasmic reticulum within the region of TIRF excitation is then calculated mathematically by subtracting the integrated density of the fluorescence at pH 5.4 from that at pH 7.4, represented in Figure 2C. This calculated plasma membrane integrated density corresponds to the relative number of SEP-labeled receptors located on the plasma membrane and within the TIRF excitation volume. Since the plasma membrane and nearby peripheral endoplasmic reticulum are being preferentially excited with TIRF, this subcellular distribution comparison is between receptors localized to these regions, and not the entire intracellular region of the cell.
Subcellular Distribution of SEP-labeled Receptors
Trafficking of receptors can be measured by comparing the ratio between receptors located on the plasma membrane compared to the endoplasmic reticulum. Dividing the plasma membrane integrated density by the total integrated density at pH 7.4, multiplied by 100, gives a relative percentage of SEP-labeled receptors located on the plasma membrane5,7. As a control, brefeldin A can be added to cells to disrupt intracellular protein trafficking. When brefeldin A is present, virtually all of the detected receptors within the region of TIRF excitation will be confined to the endoplasmic reticulum, resulting in a lower % PM. Additionally, mutated (&#916;508-I539T) cystic fibrosis transmembrane regulator (&#916;508-I539T-CFTR) can be used as a positive control. In the presence of commercially available VX-809, &#916;508-I539T-CFTR expression on the cell surface increases 2 to 3-fold.
Single Vesicle Insertion Events
SEP does not fluoresce or photobleach in the low pH of a transport vesicle, but regains fluorescence upon exposure to an extracellular pH of 7.4 at the plasma membrane7,16,18. Insertion events are visualized as a burst of fluorescence at the plasma membrane lasting at least 3 frames (600 msec), corresponding to full fusion of the transport vesicle into the plasma membrane, as shown in Figure 3. Before an insertion (Figure 3B), no discernable burst is present. An increase in fluorescence intensity is seen as the transport vesicle arrives (Figure 3C), diffusing across the membrane (Figure 3D-3G), until incorporating into the bulk fluorescence of the cell (Figure 3H-3I).
<img alt="Figure 1" src="/files/ftp_upload/55466/55466fig1.jpg" /> 
Figure 1: Schematic of TIRF Microscope. This TIRF setup utilizes a 488 nm DPSS laser for SEP excitation, fiber coupled to a stepper motor to adjust the critical angle of the excitation beam by translating the beam across the back aperture of the objective. Cells are imaged using a 60X, 1.49 NA oil immersion objective. Emission is detected using an electron-multiplying charge coupled device. <a href="https://cloudflare-jove-com.bdigitaluss.remotexs.co/files/ftp_upload/55466/55466fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" src="/files/ftp_upload/55466/55466fig2.jpg" /> 
Figure 2: Expression and Trafficking on the Plasma Membrane. An N2a cell expressing &#945;3-sep/&#946;4-wt nAChRs at pH 7.4 (A) shows receptors located on the plasma membrane and endoplasmic reticulum. At pH 5.4 (B), receptors on the plasma membrane do not fluoresce, so only the endoplasmic reticulum resident receptors are visible. The difference between integrated density at pH 7.4 and pH 5.4 (C) corresponds to receptors localized to the plasma membrane. <a href="https://cloudflare-jove-com.bdigitaluss.remotexs.co/files/ftp_upload/55466/55466fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" src="/files/ftp_upload/55466/55466fig3.jpg" /> 
Figure 3: Single Vesicle Insertion Event. An N2a cell expressing &#945;3-sep/&#946;4-wt nAChRs with an extracellular pH 7.4 is shown in (A). Immediately preceding an insertion (B), no burst of fluorescence is visible. A trafficking vesicle carrying SEP arrives (C), and SEP-labeled receptors diffuse across the plasma membrane (D-G), until indistinguishable from previously inserted receptors (H-I). <a href="https://cloudflare-jove-com.bdigitaluss.remotexs.co/files/ftp_upload/55466/55466fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Utilizing pHluorin-tagged Receptors to Monitor Subcellular Localization and Trafficking at JoVE.com

Utilizing pHluorin-tagged Receptors to Monitor Subcellular Localization and Trafficking

Labeling the extracellular domain of a membrane protein with a pH sensitive fluorophore, superecliptic pHluorin (SEP), allows subcellular localization, expression, and trafficking to be determined. Imaging SEP-labeled proteins with total internal reflection fluorescence microscopy (TIRFM) enables the quantification of protein levels in the peripheral ER and plasma membrane.

Understanding membrane protein trafficking, assembly, and expression requires an approach that differentiates between those residing in intracellular ...

utilizing-phluorin-tagged-receptors-to-monitor-subcellular

Nanyang Technological University

Research

JoVE Journal

Biology

8.7K Views.  University of Kentucky. Labeling the extracellular domain of a membrane protein with a pH sensitive fluorophore, superecliptic pHluorin (SEP), allows subcellular localization, expression, and trafficking to be determined. Imaging SEP-labeled proteins with total internal reflection fluorescence microscopy (TIRFM) enables the quantification of protein levels in the peripheral ER and plasma membrane.

Video: Utilizing pHluorin-tagged Receptors to Monitor Subcellular Localization and Trafficking

Lateral Diffusion and Exocytosis of Membrane Proteins in Cultured Neurons Assessed using Fluorescence Recovery and Fluorescence-loss Photobleaching

Membrane proteins such as receptors and ion channels undergo active trafficking in neurons, which are highly polarised and morphologically complex. This directed trafficking is of fundamental importance to deliver, maintain or remove synaptic proteins.
Super-ecliptic pHluorin (SEP) is a pH-sensitive derivative of eGFP that has been extensively used for live cell imaging of plasma membrane proteins1-2. At low pH, protonation of SEP decreases photon absorption and eliminates fluorescence emission. As most intracellular trafficking events occur in compartments with low pH, where SEP fluorescence is eclipsed, the fluorescence signal from SEP-tagged proteins is predominantly from the plasma membrane where the SEP is exposed to a neutral pH extracellular environment. When illuminated at high intensity SEP, like every fluorescent dye, is irreversibly photodamaged (photobleached)3-5. Importantly, because low pH quenches photon absorption, only surface expressed SEP can be photobleached whereas intracellular SEP is unaffected by the high intensity illumination6-10. 
FRAP (fluorescence recovery after photobleaching) of SEP-tagged proteins is a convenient and powerful technique for assessing protein dynamics at the plasma membrane. When fluorescently tagged proteins are photobleached in a region of interest (ROI) the recovery in fluorescence occurs due to the movement of unbleached SEP-tagged proteins into the bleached region. This can occur via lateral diffusion and/or from exocytosis of non-photobleached receptors supplied either by de novo synthesis or recycling (see Fig. 1). The fraction of immobile and mobile protein can be determined and the mobility and kinetics of the diffusible fraction can be interrogated under basal and stimulated conditions such as agonist application or neuronal activation stimuli such as NMDA or KCl application8,10. 
We describe photobleaching techniques designed to selectively visualize the recovery of fluorescence attributable to exocytosis. Briefly, an ROI is photobleached once as with standard FRAP protocols, followed, after a brief recovery, by repetitive bleaching of the flanking regions. This 'FRAP-FLIP' protocol, developed in our lab, has been used to characterize AMPA receptor trafficking at dendritic spines10, and is applicable to a wide range of trafficking studies to evaluate the intracellular trafficking and exocytosis.

This report describes the use of live cell imaging and photobleach techniques to determine the surface expression, transport pathways and trafficking kinetics of exogenously expressed, pH-sensitive GFP-tagged proteins at the plasma membrane of neurons.

Membrane proteins such as receptors and ion channels undergo active trafficking in neurons, which are highly polarised and morphologically complex. This ...

Neuroscience

High-resolution Spatiotemporal Analysis of Receptor Dynamics by Single-molecule Fluorescence Microscopy

Single-molecule microscopy is emerging as a powerful approach to analyze the behavior of signaling molecules, in particular concerning those aspect (e.g., kinetics, coexistence of different states and populations, transient interactions), which are typically hidden in ensemble measurements, such as those obtained with standard biochemical or microscopy methods. Thus, dynamic events, such as receptor-receptor interactions, can be followed in real time in a living cell with high spatiotemporal resolution. This protocol describes a method based on labeling with small and bright organic fluorophores and total internal reflection fluorescence (TIRF) microscopy to directly visualize single receptors on the surface of living cells. This approach allows one to precisely localize receptors, measure the size of receptor complexes, and capture dynamic events such as transient receptor-receptor interactions. The protocol provides a detailed description of how to perform a single-molecule experiment, including sample preparation, image acquisition and image analysis. As an example, the application of this method to analyze two G-protein-coupled receptors, i.e., &#946;2-adrenergic and &#947;-aminobutyric acid type B (GABAB) receptor, is reported. The protocol can be adapted to other membrane proteins and different cell models, transfection methods and labeling strategies.

This protocol describes how to use total internal reflection fluorescence microscopy to visualize and track single receptors on the surface of living cells and thereby analyze receptor lateral mobility, size of receptor complexes as well as to visualize transient receptor-receptor interactions. This protocol can be extended to other membrane proteins.

Single-molecule microscopy is emerging as a powerful approach to analyze the behavior of signaling molecules, in particular concerning those aspect (e.g., ...

Bioengineering

Imaging pHluorin-tagged Receptor Insertion to the Plasma Membrane in Primary Cultured Mouse Neurons

A better understanding of the mechanisms governing receptor trafficking between the plasma membrane (PM) and intracellular compartments requires an experimental approach with excellent spatial and temporal resolutions. Moreover, such an approach must also have the ability to distinguish receptors localized on the PM from those in intracellular compartments. Most importantly, detecting receptors in a single vesicle requires outstanding detection sensitivity, since each vesicle carries only a small number of receptors. Standard approaches for examining receptor trafficking include surface biotinylation followed by biochemical detection, which lacks both the necessary spatial and temporal resolutions; and fluorescence microscopy examination of immunolabeled surface receptors, which requires chemical fixation of cells and therefore lacks sufficient temporal resolution1-6 . To overcome these limitations, we and others have developed and employed a new strategy that enables visualization of the dynamic insertion of receptors into the PM with excellent spatial and temporal resolutions 7-17 . The approach includes tagging of a pH-sensitive GFP, the superecliptic pHluorin 18, to the N-terminal extracellular domain of the receptors. Superecliptic pHluorin has the unique property of being fluorescent at neutral pH and non-fluorescent at acidic pH (pH &lt; 6.0). Therefore, the tagged receptors are non-fluorescent when within the acidic lumen of intracellular trafficking vesicles or endosomal compartments, and they become readily visualized only when exposed to the extracellular neutral pH environment, on the outer surface of the PM. Our strategy consequently allows us to distinguish PM surface receptors from those within intracellular trafficking vesicles. To attain sufficient spatial and temporal resolutions, as well as the sensitivity required to study dynamic trafficking of receptors, we employed total internal reflection fluorescent microscopy (TIRFM), which enabled us to achieve the optimal spatial resolution of optical imaging (~170 nm), the temporal resolution of video-rate microscopy (30 frames/sec), and the sensitivity to detect fluorescence of a single GFP molecule. By imaging pHluorin-tagged receptors under TIRFM, we were able to directly visualize individual receptor insertion events into the PM in cultured neurons. This imaging approach can potentially be applied to any membrane protein with an extracellular domain that could be labeled with superecliptic pHluorin, and will allow dissection of the key detailed mechanisms governing insertion of different membrane proteins (receptors, ion channels, transporters, etc.) to the PM.

By tagging the extracellular domains of membrane receptors with superecliptic pHluorin, and by imaging these fusion receptors in cultured mouse neurons, we can directly visualize individual vesicular insertion events of the receptors to the plasma membrane. This technique will be instrumental in elucidating the molecular mechanisms governing receptor insertion to the plasma membrane.

A better understanding of the mechanisms governing receptor trafficking between the plasma membrane (PM) and intracellular compartments requires an ...

Use of pHluorin to Assess the Dynamics of Axon Guidance Receptors in Cell Culture and in the Chick Embryo

During development, axon guidance receptors play a crucial role in regulating axons sensitivity to both attractive and repulsive cues. Indeed, activation of the guidance receptors is the first step of the signaling mechanisms allowing axon tips, the growth cones, to respond to the ligands. As such, the modulation of their availability at the cell surface is one of the mechanisms that participate in setting the growth cone sensitivity. We describe here a method to precisely visualize the spatio-temporal cell surface dynamics of an axon guidance receptor both in vitro and in vivo in the developing chick spinal cord. We took advantage of the pH-dependent fluorescence property of a green fluorescent protein (GFP) variant to specifically detect the fraction of the axon guidance receptor that is addressed to the plasma membrane. We first describe the in vitro validation of such pH-dependent constructs and we further detail their use in vivo, in the chick spinal chord, to assess the spatio-temporal dynamics of the axon guidance receptor of interest.

We describe here the use of a pH-sensitive green fluorescent protein variant, pHluorin, to study the spatio-temporal dynamics of axon guidance receptors trafficking at the cell surface.&#160;The pHluorin-tagged receptor is expressed both in cell culture and in vivo, using electroporation of the chick embryo.

During development, axon guidance receptors play a crucial role in regulating axons sensitivity to both attractive and repulsive cues. Indeed, activation ...

A High-content Assay for Monitoring AMPA Receptor Trafficking

Postsynaptic trafficking of receptors to and from the cell surface is an important mechanism by which neurons modulate their responsiveness to different stimuli. The &#945;-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, which are responsible for fast excitatory synaptic transmission in neurons, are trafficked to and from the postsynaptic surface to dynamically alter neuronal excitability. AMPA receptor trafficking is essential for synaptic plasticity and can be disrupted in neurological disease. However, prevalent approaches for quantifying receptor trafficking ignore entire receptor pools, are overly time- and labor-intensive, or potentially disrupt normal trafficking mechanisms and therefore complicate the interpretation of resulting data. We present a high-content assay for the quantification of both surface and internal AMPA receptor populations in cultured primary hippocampal neurons using dual fluorescent immunolabeling and a near-infrared fluorescent 96-well microplate scanner. This approach facilitates the rapid screening of bulk internalized and surface receptor densities while minimizing sample material. However, our method has limitations in obtaining single-cell resolution or conducting live cell imaging. Finally, this protocol may be amenable to other receptors and different cell types, provided proper adjustments and optimization.

Neuronal excitability can be modulated through a dynamic process of endo- and exocytosis of excitatory ionotropic glutamate receptors. Described here is an accessible, high-content assay for quantifying surface and internal receptor population pools.

Postsynaptic trafficking of receptors to and from the cell surface is an important mechanism by which neurons modulate their responsiveness to different ...

Visualization of Endoplasmic Reticulum Subdomains in Cultured Cells

The lipids and proteins in eukaryotic cells are continuously exchanged between cell compartments, although these retain their distinctive composition and functions despite the intense interorganelle molecular traffic. The techniques described in this paper are powerful means of studying protein and lipid mobility and trafficking in vivo and in their physiological environment. Fluorescence recovery after photobleaching (FRAP) and fluorescence loss in photobleaching (FLIP) are widely used live-cell imaging techniques for studying intracellular trafficking through the exo-endocytic pathway, the continuity between organelles or subcompartments, the formation of protein complexes, and protein localization in lipid microdomains, all of which can be observed under physiological and pathological conditions. The limitations of these approaches are mainly due to the use of fluorescent fusion proteins, and their potential drawbacks include artifactual over-expression in cells and the possibility of differences in the folding and localization of tagged and native proteins. Finally, as the limit of resolution of optical microscopy (about 200 nm) does not allow investigation of the fine structure of the ER or the specific subcompartments that can originate in cells under stress (i.e. hypoxia, drug administration, the over-expression of transmembrane ER resident proteins) or under pathological conditions, we combine live-cell imaging of cultured transfected cells with ultrastructural analyses based on transmission electron microscopy.

We describe the imaging approaches we use to investigate the distribution and mobility of the transfected fluorescent proteins resident in the endoplasmic reticulum (ER) by means of the confocal imaging of living cells. We also ultrastructurally analyze the effect of their expression on the architecture of this subcellular compartment.

The lipids and proteins in eukaryotic cells are continuously exchanged between cell compartments, although these retain their distinctive composition and ...

Visualizing Clathrin-mediated Endocytosis of G Protein-coupled Receptors at Single-event Resolution via TIRF Microscopy

Many important signaling receptors are internalized through the well-studied process of clathrin-mediated endocytosis (CME). Traditional cell biological assays, measuring global changes in endocytosis, have identified over 30 known components participating in CME, and biochemical studies have generated an interaction map of many of these components. It is becoming increasingly clear, however, that CME is a highly dynamic process whose regulation is complex and delicate. In this manuscript, we describe the use of Total Internal Reflection Fluorescence (TIRF) microscopy to directly visualize the dynamics of components of the clathrin-mediated endocytic machinery, in real time in living cells, at the level of individual events that mediate this process. This approach is essential to elucidate the subtle changes that can alter endocytosis without globally blocking it, as is seen with physiological regulation. We will focus on using this technique to analyze an area of emerging interest, the role of cargo composition in modulating the dynamics of distinct clathrin-coated pits (CCPs). This protocol is compatible with a variety of widely available fluorescence probes, and may be applied to visualizing the dynamics of many cargo molecules that are internalized from the cell surface.

Clathrin-mediated endocytosis, a rapid and highly dynamic process internalizes many proteins, including signaling receptors. The protocol described here directly visualizes the kinetics of individual endocytic events. This is essential for understanding how core members of the endocytic machinery coordinate with each other, and how protein cargo influence this process.

Many important signaling receptors are internalized through the well-studied process of clathrin-mediated endocytosis (CME). Traditional cell biological ...

Tracking Drug-induced Changes in Receptor Post-internalization Trafficking by Colocalizational Analysis

The intracellular trafficking of receptors is a collection of complex and highly controlled processes. Receptor trafficking modulates signaling and overall cell responsiveness to ligands and is, itself, influenced by intra- and extracellular conditions, including ligand-induced signaling. Optimized for use with monolayer-plated cultured cells, but extendable to free-floating tissue slices, this protocol uses immunolabelling and colocalizational analysis to track changes in intracellular receptor trafficking following both chronic/prolonged and acute interventions, including exogenous drug treatment. After drug treatment, cells are double-immunolabelled for the receptor and for markers for the intracellular compartments of interest. Sequential confocal microscopy is then used to capture two-channel photomicrographs of individual cells, which are subjected to computerized colocalizational analysis to yield quantitative colocalization scores. These scores are normalized to permit pooling of independent replicates prior to statistical analysis. Representative photomicrographs may also be processed to generate illustrative figures. Here, we describe a powerful and flexible technique for quantitatively assessing induced receptor trafficking.

Receptor trafficking modulates signaling and cell responsiveness to ligands and is, itself, responsive to cell conditions, including ligand-induced signaling. Here, we describe a powerful and flexible technique for quantitatively assessing drug-induced receptor trafficking using immunolabeling and colocalizational analysis.

The intracellular trafficking of receptors is a collection of complex and highly controlled processes. Receptor trafficking modulates signaling and ...

Applications of pHluorin for Quantitative, Kinetic and High-throughput Analysis of Endocytosis in Budding Yeast

Green fluorescent protein (GFP) and its variants are widely used tools for studying protein localization and dynamics of events such as cytoskeletal remodeling and vesicular trafficking in living cells. Quantitative methodologies using chimeric GFP fusions have been developed for many applications; however, GFP is somewhat resistant to proteolysis, thus its fluorescence persists in the lysosome/vacuole, which can impede quantification of cargo trafficking in the endocytic pathway. An alternative method for quantifying endocytosis and post-endocytic trafficking events makes use of superecliptic pHluorin, a pH-sensitive variant of GFP that is quenched in acidic environments. Chimeric fusion of pHluorin to the cytoplasmic tail of transmembrane cargo proteins results in a dampening of fluorescence upon incorporation of the cargo into multivesicular bodies (MVBs) and delivery to the lysosome/vacuole lumen. Thus, quenching of vacuolar fluorescence facilitates quantification of endocytosis and early events in the endocytic pathway. This paper describes methods using pHluorin-tagged cargos for quantification of endocytosis via fluorescence microscopy, as well as population-based assays using flow cytometry.

Accurate quantification of vesicular trafficking events often provides key insights into roles for specific proteins and the effects of mutations. This paper presents methods for using superecliptic pHluorin, a pH-sensitive GFP variant, as a tool for quantification of endocytic events in living cells using quantitative fluorescence microscopy and flow cytometry.

Green fluorescent protein (GFP) and its variants are widely used tools for studying protein localization and dynamics of events such as cytoskeletal ...

Live Cell Imaging and 3D Analysis of Angiotensin Receptor Type 1a Trafficking in Transfected Human Embryonic Kidney Cells Using Confocal Microscopy

Live-cell imaging is used to simultaneously capture time-lapse images of angiotensin type 1a receptors (AT1aR) and intracellular compartments in transfected human embryonic kidney-293 (HEK) cells following stimulation with angiotensin II (Ang II). HEK cells are transiently transfected with plasmid DNA containing AT1aR tagged with enhanced green fluorescent protein (EGFP). Lysosomes are identified with a red fluorescent dye. Live-cell images are captured on a laser scanning confocal microscope after Ang II stimulation and analyzed by software in three dimensions (3D, voxels) over time. Live-cell imaging enables investigations into receptor trafficking and avoids confounds associated with fixation, and in particular, the loss or artefactual displacement of EGFP-tagged membrane receptors. Thus, as individual cells are tracked through time, the subcellular localization of receptors can be imaged and measured. Images must be acquired sufficiently rapidly to capture rapid vesicle movement. Yet, at faster imaging speeds, the number of photons collected is reduced. Compromises must also be made in the selection of imaging parameters like voxel size in order to gain imaging speed. Significant applications of live-cell imaging are to study protein trafficking, migration, proliferation, cell cycle, apoptosis, autophagy and protein-protein interaction and dynamics, to name but a few.

Here we present a protocol to image cells expressing green fluorescent protein-tagged angiotensin type 1a receptors during endocytosis initiated by angiotensin II treatment. This technique includes labeling lysosomes with a second fluorescent marker, and then utilizing software to analyze the co-localization of receptor and lysosome in three dimensions over time.