Rab10 Phosphorylation Detection by LRRK2 Activity Using SDS-PAGE with a Phosphate-binding Tag

Summary

The present study describes a simple method of detecting endogenous levels of Rab10 phosphorylation by leucine-rich repeat kinase 2.

Abstract

Mutations in leucine-rich repeat kinase 2 (LRRK2) have been shown to be linked with familial Parkinson's disease (FPD). Since abnormal activation of the kinase activity of LRRK2 has been implicated in the pathogenesis of PD, it is essential to establish a method to evaluate the physiological levels of the kinase activity of LRRK2. Recent studies revealed that LRRK2 phosphorylates members of the Rab GTPase family, including Rab10, under physiological conditions. Although the phosphorylation of endogenous Rab10 by LRRK2 in cultured cells could be detected by mass spectrometry, it has been difficult to detect it by immunoblotting due to the poor sensitivity of currently available phosphorylation-specific antibodies for Rab10. Here, we describe a simple method of detecting the endogenous levels of Rab10 phosphorylation by LRRK2 based on immunoblotting utilizing sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) combined with a phosphate-binding tag (P-tag), which is N-(5-(2-aminoethylcarbamoyl)pyridin-2-ylmetyl)-N,N',N'-tris(pyridin-2-yl-methyl)-1,3-diaminopropan-2-ol. The present protocol not only provides an example of the methodology utilizing the P-tag but also enables the assessment of how mutations as well as inhibitor treatment/administration or any other factors alter the downstream signaling of LRRK2 in cells and tissues.

Introduction

PD is one of the most common neurodegenerative diseases, predominantly affecting dopaminergic neurons in the midbrain, resulting in dysfunction of the motor systems in elderly people¹. While most patients develop PD in a sporadic manner, there are families inheriting the disease. Mutations in several genes have been found to be linked with FPD². One of the causative genes for FPD is LRRK2, in which eight missense mutations (N1437H, R1441C/G/H/S, Y1699C, G2019S, and I2020T) linked to a dominantly inherited FPD called PARK8 have so far been reported^3,4,5. Several genome-wide association studies (GWAS) of sporadic PD patients have also identified genomic variations at the LRRK2 locus as a risk factor for PD, suggesting that abnormality in the function of LRRK2 is a common cause of neurodegeneration in both sporadic and PARK8 FPD^6,7,8.

LRRK2 is a large protein (2,527 amino acids) consisting of a leucine-rich repeat domain, a GTP-binding Ras of complex proteins (ROC) domain, a C-terminal of ROC (COR) domain, a serine/threonine protein kinase domain, and a WD40 repeat domain⁹. The eight FPD mutations locate in these functional domains; N1437H and R1441C/G/H/S in the ROC domain, Y1699C in the COR domain, G2019S and I2020T in the kinase domain. Since G2019S mutation, which is the most frequently found mutation in PD patients^10,11,12, increases the kinase activity of LRRK2 by 2 - 3 fold in vitro¹³, it is hypothesized that the abnormal increase in phosphorylation of LRRK2 substrate(s) is toxic to neurons. However, it has been impossible to study whether the phosphorylation of physiologically relevant LRRK2 substrates is altered in familial/sporadic PD patients due to the lack of methods evaluating it in patient derived samples.

Protein phosphorylation is generally detected by immunoblotting or enzyme-linked immunosorbent assay (ELISA) using antibodies specifically recognizing the phosphorylated state of proteins or by mass spectrometric analysis. However, the former strategy sometimes cannot be applied because of the difficulties in creating phosphorylation-specific antibodies. Metabolic labeling of cells with radioactive phosphate is another option to examine physiological levels of phosphorylation when phosphorylation-specific antibodies are not readily available. However, it requires a large amount of radioactive materials and therefore involves some specialized equipment for radioprotection¹⁴. Mass spectrometric analysis is more sensitive compared to these immunochemical methods and became popular in analyzing protein phosphorylation. However, the sample preparation is time-consuming, and expensive instruments are required for the analysis.

A subset of the Rab GTPase family including Rab10 and Rab8 was recently reported as direct physiological substrates for LRRK2 based on the result of a large-scale phosphoproteomic analysis¹⁵. We then demonstrated that Rab10 phosphorylation was increased by FPD mutations in mouse embryonic fibroblasts and in the lungs of knockin mice¹⁶. In this report, we chose to employ a sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE)-based method in which a P-tag molecule is co-polymerized into SDS-PAGE gels (P-tag SDS-PAGE) for detecting the endogenous levels of Rab10 phosphorylation, because a highly sensitive antibody specific for phosphorylated Rab10 was still lacking. We have failed to detect the phosphorylation of endogenous Rab8 due to the poor selectivity of currently available antibodies for total Rab8. Therefore, we decided to focus on the Rab10 phosphorylation. LRRK2 phosphorylates Rab10 at Thr73 locating at the middle of the highly conserved "switch II" region. High conservation of the phosphorylation sites among Rab proteins might be one of the reasons why phosphospecific antibodies recognizing distinct Rab proteins are difficult to make.

The phosphorylation of Rab8A by LRRK2 inhibits the binding of Rabin8, a guanine nucleotide exchange factor (GEF) which activates Rab8A by exchanging the bound GDP with GTP¹⁵. Phosphorylation of Rab10 and Rab8A by LRRK2 also inhibits the binding of GDP-dissociation inhibitors (GDIs), which are essential to the activation of Rab proteins by extracting GDP-bound Rab proteins from membranes¹⁵. Collectively, it is hypothesized that the phosphorylation of Rab proteins by LRRK2 prevents them from activation although the precise molecular mechanism and physiological consequences of the phosphorylation remain unclear.

P-tag SDS-PAGE was invented by Kinoshita et al. in 2006: In this method, acrylamide was covalently coupled with P-tag, a molecule capturing phosphates with high affinity, which copolymerized into SDS-PAGE gels¹⁷. Because the P-tag molecules in a SDS-PAGE gel selectively retard electrophoretic mobility of phosphorylated proteins, P-tag SDS-PAGE can separate phosphorylated proteins from non-phosphorylated ones (Figure 1). If the protein-of-interest is phosphorylated on multiple residues, a ladder of bands corresponding to differentially phosphorylated forms will be observed. In the case of Rab10, we observe only one shifted band, indicating that Rab10 is phosphorylated only at Thr73. The major advantage of P-tag SDS-PAGE over immunoblotting with phosphorylation-specific antibodies is that phosphorylated Rab10 can be detected by immunoblotting with non-phosphorylation-specific antibodies (i.e., recognizing total Rab10) after being transferred on membranes, which is generally more specific, sensitive, and available from commercial/academic sources. Another advantage of using P-tag SDS-PAGE is that one can obtain approximate estimation of the stoichiometry of phosphorylation, which is impossible by immunoblotting with phosphorylation-specific antibodies or by metabolic labeling of cells with radioactive phosphates.

Apart from the use of inexpensive P-tag acrylamide and some minor modifications related to it, the present method for detection of Rab10 phosphorylation by LRRK2 follows a general protocol of immunoblotting. Therefore, it should be straightforward and easily executable in any laboratories where immunoblotting is a usual practice, with any types of samples including purified proteins, cell lysates, and tissue homogenates.

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Protocol

1. Sample Preparation for the P-tag SDS–PAGE

1. Remove and discard the media from 10 cm dishes in which cells are grown using a suction and wash cells with 5 mL Dulbecco's phosphate-buffered saline (DPBS) by first adding DPBS to the side of the dishes to avoid disturbing the cell layer, and manually rock the dishes back and forth several times.
2. Remove and discard the DPBS using a suction and add 2 mL of 0.25% (w/v) trypsin diluted in DPBS, and gently rock the dishes to cover the cell layer. Put the dishes into a CO₂ incubator (37 °C, humidified air, 5% CO₂) for 5 min.
3. After pipetting up and down using a disposable pipette to break up detached cells, collect the cell suspension into a 15 mL tube and measure the cell density using a hematocytometer under a microscope¹⁸.
4. Dilute the cells to 2.5 × 10⁵ cells/mL with Dulbecco's modified Eagle medium (DMEM) supplemented with 10% (v/v) fetal bovine serum (FBS), 100 U/mL penicillin, and 100 µg/mL streptomycin. Add 2 mL (5 × 10⁵ cells) of the diluted cell suspension to each well of 6-well plates.
5. Grow the cells overnight in a CO₂ incubator (37 °C, humidified air, 5% CO₂).
6. Transfection into HEK293 cells
   NOTE: If phosphorylation of endogenous Rab10 is to be examined, proceed to step 1.7. Plasmids used in this protocol can be obtained from the authors upon request. See Table of Materials for brief information and Figure S1 for their DNA sequences.
   1. Aliquot 200 µL of DMEM into 1.5 mL tubes.
   2. To each tube, add both 0.266 µg (final concentration of 1.33 µg/mL) of a plasmid encoding HA-Rab10 and 1.066 µg (final concentration of 5.33 µg/mL) of a plasmid encoding 3×FLAG-LRRK2 from 500 µg/mL plasmid stocks. Then add 4 µL of 1 mg/mL solution of polyethyleneimine (dissolved in 20 mM HEPES-NaOH, pH 7.0) and immediately mix the solution by vortexing for 5 s.
   3. Let the tubes stand at room temperature for 10 min and add the content of one tube dropwise to one well using a micropipette. Gently and manually rock the culture plates back and forth several times to let the transfection mixture diffuse evenly throughout the well.
7. Let the cells grow for another 24-36 h in a CO₂ incubator (37 °C, humidified air, 5% CO₂).
8. If phosphorylation of endogenous Rab10 is to be examined, treat cells with and without LRRK2 inhibitors for 1 h before lysing cells.
   1. Prepare stock solutions of LRRK2 inhibitors by dissolving the inhibitors in dimethyl sulfoxide (DMSO) at 10 mM. We recommend using MLi-2 and GSK2578215A, which are highly specific and potent LRRK2 inhibitors. Store stock solutions at -80 °C.
   2. Prepare working stocks of the inhibitors by diluting the stock solutions with DMSO: For MLi-2, prepare 10 µM and 30 µM for endogenous and overexpressed LRRK2, respectively. For GSK2578215A, prepare 1 mM and 3 mM for endogenous and overexpressed LRRK2, respectively.
   3. Add 2 µL of the working stocks of either MLi-2 or GSK2578215A to the middle of one well using a micropipette and gently rock the plate manually back and forth several times to let the inhibitors diffuse evenly throughout the well.
   4. Add 2 µL of DMSO to a different well as a negative control in a similar manner to the inhibitor in step 1.8.3.
   5. Put the plates back to the incubator and culture the cells for 1 h.
9. Lyse the cells.
   1. Put the culture plates on ice. Remove and discard the media. Wash the cells by first adding 2 mL DPBS to the side of the dishes to avoid disturbing the cell layer and manually rock the dishes back and forth several times.
   2. Remove and discard the DPBS, and add to the cells 100 µL of the lysis buffer (50 mM Tris-HCl pH 7.5, 1% (v/v) polyoxyethylene(10) octylphenyl ether, 1 mM EGTA (ethylene glycol-bis(2-aminoethylether)-N,N,N',N'-tetraacetic acid), 1 mM sodium orthovanadate, 50 mM sodium fluoride, 10 mM β-glycerophosphate, 5 mM sodium pyrophosphate, 0.1 µg/mL microcystin-LR, 270 mM sucrose, protease inhibitor cocktail).
   3. Tilt the plates on ice and scrape the cells using a cell scraper to gather as much cell lysate as possible. Collect the lysates using a micropipette into 1.5 mL tubes (pre-chilled on ice).
      Caution: Microcystin-LR can be fatal if swallowed or in contact with skin.
10. Let the tubes stand on ice for 10 min for complete lysis. Clarify the cell lysates by centrifugation (20,000 × g, 10 min at 4 °C) and transfer the supernatants to new 1.5 mL tubes pre-chilled on ice.
11. Measure protein concentration (µg/µL) of the cleared lysates by Bradford assay.
    1. Prepare bovine serum albumin (BSA) standards (0.2, 0.4, 0.6, 0.8, and 1 mg/mL) by diluting the stock solution with distilled water. Dilute the cleared cell lysates by 20-fold with distilled water.
    2. Put 5 µL/well of the BSA standards, blank (distilled water), and each diluted cell lysate into a 96-well plate in triplicate.
    3. Add 150 µL/well of the Bradford assay reagent using 12-channel micropipette and let the plate stand at room temperature for 5 min.
    4. Measure the absorbance at 595 nm on a plate reader and compare to BSA standards.
12. Prepare 100 µL of samples for SDS-PAGE. The protein concentration of the samples is 1 µg/µL for overexpressed HA-Rab10 and 2 µg/µL for endogenous Rab10.
    1. Using the quantified concentrations from step 1.11.4, calculate the volume (µL) of the cell lysates equivalent to 100 µg (overexpressed HA-Rab10) or 200 µg (endogenous Rab10) by dividing the protein amount (100 µg or 200 µg) by the protein concentration of lysates (µg/µL).
    2. Add 25 µL of 4× Laemmli's SDS-PAGE sample buffer (62.5 mM Tris-HCl, pH 6.8, 8% (w/v) SDS, 40% (v/v) glycerol, 0.02% (w/v) bromophenol blue, 4% (v/v) β-mercaptoethanol) to new 1.5 mL tubes kept at room temperature.
    3. Add the calculated volume of the cell lysates to each tube and mix by vortexing for 5 s at room temperature.
    4. Bring the total volume to 100 µL with the lysis buffer and mix by vortexing for 5 s at room temperature.
13. Supplement with 10 mM MnCl₂ to quench the chelating agent. Add 1 µL of 500 mM MnCl₂. Mix by vortexing for 5 s at room temperature.
    NOTE: Samples containing MnCl₂ may not be suitable for normal SDS-PAGE. This step is required due to the presence of the chelating agent (such as ethylenediaminetetraacetic acid (EDTA), EGTA, etc.) in the lysis buffer. Otherwise, Mn²⁺ ions coupled to P-tag acrylamide will be dissociated by the chelating agents, and P-tag SDS-PAGE will not work properly.
14. Boil all samples at 100 °C for 5 min and store the samples below -20 °C until use. The boiled samples can be stored up to at least 6 months.

2. Casting Gels for P-tag SDS–PAGE

NOTE: Gels should be made on the same day as running the gels. Gels can be made under ambient light conditions.

1. Prepare 5 mM P-tag acrylamide stock solution by first dissolving the 10 mg of powder/solid P-tag acrylamide completely with 100 µL of methanol and then bring to 3.3 mL by adding double distilled water.
   NOTE: P-tag acrylamide is light sensitive. The prepared solution should be stored in the dark at 4 °C until use.
2. Clean both plain and notched plates by spraying 70% ethanol and wiping with a paper towel. Assemble the gel plates. The dimensions of the gel plates used in this particular protocol are 80 or 100 mm long by 100 mm wide. Clean silicon spacers are put in between plain and notched plates and the assembled plates are clamped with binder clips.
   NOTE: Any type of gel plates that work for ordinary SDS-PAGE can be used.
3. Put a comb to be used (17-well plastic comb) into the assembled gel plates and mark on the gel plate the position of the bottom of the wells with a permanent marker.
4. Prepare 10 mL of 10% acrylamide gel mixture (10% (w/v) acrylamide (acrylamide:bis-acrylamide = 29:1), 375 mM Tris-HCl (pH 8.8), 0.1% (w/v) SDS) in a 15 mL tube.
   NOTE: The optimal concentration of acrylamide may vary depending on the reagents used. Tetramethylethylenediamine (TEMED) and ammonium persulfate (APS) should not be added at this point.
5. Add 100 µL of 5 mM P-tag acrylamide and 10 µL of 1 M MnCl₂ solutions at final concentrations of 50 µM and 100 µM, respectively.
   NOTE: The optimal concentrations of the P-tag acrylamide and MnCl₂ might also vary depending on the reagents used.
6. Add 15 µL of TEMED to the gel mixture at a final concentration of 0.15% (v/v) and then 50 µL of 10% (w/v) APS at a final concentration of 0.05% (w/v). Mix well by gently swirling the tube for 5 s and pour into the assembled plates immediately up to a height that is 2 mm below the position marked in step 2.3.
7. Gently layer 2-propanol onto the gel solution to flatten the top of separating gels.
8. Let the gels stand for 30 min at room temperature. It is not necessary to protect the gels from light.
   NOTE: It might take longer for gels to set under cold room temperature. Degassing the gel mixture before adding TEMED and APS helps accelerate this step. For this purpose, the gel mixture can be prepared in a 100-200 mL Erlenmeyer flask connected to a suction. Degas the solution for 10 min.
9. Remove the layered 2-propanol by absorbing with a paper towel.
10. Wash the top space of the gels by filling the space up with distilled water from a wash bottle and discard the water by pouring off into basin. Repeat washing 3 times.
11. Remove residual water remaining in the top space of the gels by absorbing with a paper towel.
12. Prepare 3 mL of 4% acrylamide gel mixture (4% (w/v) acrylamide (a: crylamide:bis-acrylamide = 29:1), 125 mM Tris-HCl (pH 6.8), 0.1% (w/v) SDS) in a 15 mL tube.
    NOTE: Do not add P-tag acrylamide or MnCl₂ solution to the stacking gel mixture.
13. Add 7.5 µL of TEMED and 24 µL of 10% (w/v) APS at final concentrations of 0.25% (v/v) and 0.08% (w/v), respectively. Mix well by gently swirling the tube for 5 s and pour the mixture on top of the separation gel. Immediately put appropriate combs (17-well plastic combs which accommodate up to 25 µL of samples, for example).
14. Let the gels stand for 30 min at room temperature. It is not necessary to protect the gels from light. After the stacking gels set, run them without further storage.

3. SDS–PAGE and Immunoblotting

1. Remove the combs from the gels. Then remove the silicon spacers and then clips from the gels.
2. Put the casted gels into gel tanks and fix the gel to the tank by clamping with the binder clips.
3. Pour the running buffer (25 mM Tris, 192 mM Glycine, 0.1% (w/v) SDS) at the bottom and top of the gels. Clean wells by flushing the running buffer using a 5 mL syringe and a 21G needle to remove gel pieces.
4. Remove air bubbles from the bottom space of the gels using a bent needle attached to a syringe. To make a bent needle, manually bend a 21G needle in the middle of the needle so that the angle between the tip and the base of the needle becomes 30-45 °.
5. Spin down precipitates caused by the addition of MnCl₂ at 20,000 × g for 1 min at room temperature to obtain clear samples.
6. Load 10 µg proteins for detecting the phosphorylation of overexpressed Rab10 and 30 µg proteins for endogenous Rab10.
   NOTE: It is critical to load equal volume of samples in ALL wells. Empty lanes should be loaded with 1× Laemmli's SDS-PAGE sample buffer. If the samples contain MnCl₂, add the same concentration of MnCl₂ to the dummy samples.
7. The well loaded with a molecular weight marker (MWM) should also be supplemented with 1× Laemmli's SDS-PAGE sample buffer so the volume of samples loaded is the same in all wells.
   NOTE: Again, if the samples contain MnCl₂, add the same concentration of MnCl₂ to the MWM. Alternatively, an EDTA-free MWM can be used.
8. Run gels at 50 V for stacking (approximately 30 min) until the dye front crosses into the separation gel.
9. After the samples stack, change the voltage to 120 V for separation until the dye front reaches the bottom of the gels (approximately 50 and 80 min for 80 and 100 mm long gels, respectively).
   NOTE: The migration pattern of the MWM is expected to be different from that on normal SDS-PAGE gels. It should not be used for estimating the molecular weight of proteins on P-tag SDS-PAGE gels but can be used for checking the reproducibility of P-tag gels. Refer to Discussion for details.
10. Wash the gels to remove MnCl₂ from the gels.
    1. Pour the transfer buffer (48 mM Tris, 39 mM Glycine, 20% (v/v) methanol) containing 10 mM EDTA and 0.05% (w/v) SDS into a container (e.g., large weighing boats). The volume of the buffer should be sufficient to cover a gel.
    2. Remove the separation gels from the gel plates and put one gel in one container. Discard the stacking gel.
    3. Leave the gels on a rocking shaker (~60 rpm) for 10 min at room temperature.
    4. Repeat the wash steps in total 3 times.
       NOTE: Use fresh buffer for each wash.
    5. Wash the gels once for 10 min with the transfer buffer containing 0.05% (w/v) SDS to remove EDTA. The volume of the buffer should be sufficient to cover a gel.
11. Electro-transfer to nitrocellulose or polyvinylidene difluoride (PVDF) membranes using wet tanks.
    1. Place a filter paper (10 x 7 cm) on a sponge pad for transfer. Place the gel on the filter paper. Make sure there are no air bubbles between the filter paper and the gel.
    2. Put a membrane (10 x 7 cm) on the gel and make sure there are no air bubbles between the gel and the membrane.
    3. Put another filter paper (10 x 7 cm) on the membrane and, again, make sure there are no air bubbles between the membrane and the filter paper.
    4. Put another sponge pad on the filter paper. Put the stack of membrane/filter papers in a cassette for transfer.
    5. Put the cassette into a transfer tank, making sure that the membrane is located between the gel and the positively charged anode.
    6. Connect the tank to a power supply and put the tank in a styrene foam box filled with ice-cold water. Start transfer at 100 V for 180 min.
       NOTE: Prolonged transfer is necessary since the transfer of proteins from P-tag SDS-PAGE gels are not as efficient as that from normal SDS-PAGE gels. Efficient cooling is essential to avoid melting gels during transfer.
12. Check the transfer
    1. Remove the membranes from the gels using tweezers and soak the membranes in a Ponceau S solution (0.1% (w/v) Ponceau S, 5% (v/v) acetic acid) to stain transferred proteins on the membranes in a plastic container. The volume of the solution should be sufficient to cover a membrane.
    2. Incubate the membranes for 1 min at room temperature by rocking manually.
       NOTE: A ladder of bands should become visible in each lane.
    3. Pick the membrane up out of the staining solution with tweezers and see if the ladder of bands has uniform pattern and intensity in every lane where the samples have been loaded.
    4. After checking the staining, remove the staining solution and add TBST buffer (20 mM Tris-HCl pH 7.4, 150 mM NaCl, 0.1% (v/v) polyoxyethylenesorbitan monolaurate). The volume of the buffer should be sufficient to cover a membrane.
       NOTE: The Ponceau S solution can be collected and re-used several times.
    5. Rock the membranes in TBST on a rocking shaker (~60 rpm) at room temperature until no visible bands remain on the membranes.
    6. Repeat the washing step with fresh TBST for 5 min.
13. Remove and discard the TBST. Block by adding 5% (w/v) skim milk dissolved in TBST and rocking on a shaker (~60 rpm) for 1 h at room temperature. The volume of the blocking solution should be sufficient to cover a membrane.
14. Prepare primary antibody solutions by diluting primary antibodies (anti-Rab10 antibody for endogenous Rab10 and anti-HA antibody for overexpressed HA-Rab10) in 10 mL per membrane of the blocking solution (see Table of Materials for concentrations).
15. Remove and discard the blocking solution and add the primary antibody. Incubate the membranes on a rocking shaker (~60 rpm) overnight at 4 °C.
16. Remove the primary antibody solution and add TBST to wash the membranes. The volume of the buffer should be sufficient to cover a membrane.
17. Incubate the membranes for 5 min on a rocking shaker (~60 rpm) at room temperature. Repeat the wash (step 3.16) in total 3 times using fresh TBST each time.
18. Prepare secondary antibody solutions by diluting secondary antibody labeled with horseradish peroxidase (HRP) in 10 mL per membrane of the blocking solution. Use anti-rabbit IgG antibody labeled with HRP for membranes probed with the anti-Rab10 antibody, and anti-mouse IgG antibody labeled with HRP for those probed with the anti-HA antibody (see Table of Materials for concentration).
19. Remove and discard the TBST after the third wash and add the secondary antibody solution. Incubate the membranes on a rocking shaker (~60 rpm) for 1 h at room temperature.
20. Wash the membranes in TBST for 10 min. Repeat the wash step in total 3 times, similar to step 3.17.
21. Develop the membranes using enhanced chemiluminescence (ECL).
    NOTE: Exposure time might vary depending on the ECL solution and the system used for detection of chemiluminescence.
    1. Turn on an imager equipped with a charge-coupled device (CCD) camera and a computer connected to the imager. Start up the control software for the imager. Wait until the temperature of the CCD camera has reached -25 °C.
    2. Put 1 mL of the ECL solution for one membrane on a plastic wrap spread on a bench.
    3. Put a membrane gel-side-up on the ECL solution and then quickly flip it over so that both sides of the membrane are coated with the solution.
    4. Pick the membrane up and drain it by letting one side of the membrane touch a paper towel for 5 s.
    5. Put the membrane between clear films (e.g., clear paper pockets).
       NOTE: Plastic wrap is not recommended for wrapping the membranes. The clear films used for wrapping the membrane need to be as flat as possible without visible wrinkles to avoid uneven background.
    6. Place the membrane on a black tray. Put the tray in the imager and close the door.
    7. Click the "Focusing" button in the window of the control software. Check that the membrane is correctly positioned. Click the "Return" button.
    8. Select "Precision" for "Exposure Type". Select "Manual" for "Exposure Time" and set the exposure time to 1 s.
    9. Select "High" for "Sensitivity/Resolution". Leave "Add Digitization Image" unchecked. Click the "Start" button to take an image.
    10. Save the image that appeared on the display in the computer as a TIFF file.
    11. Repeat taking images with the exposure time from 1, 3, 10, 30, 60, 90, 120, 150 s and up to 180 s. When taking the last image, check "Add Digitization Image" so the digital image, not the chemiluminescence, of the membrane can be simultaneously taken.
    12. Select the best image with the largest dynamic range and without any saturating pixels (shown in red) in the bands of interest.
        NOTE: Conventional X-ray films can also be used for detection¹⁹.

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Results

Overexpression System: Phosphorylation of HA-Rab10 by 3×FLAG-LRRK2 in HEK293 Cells:

HEK293 cells were transfected with 0.266 µg of HA-Rab10 wild-type and 1.066 µg of 3×FLAG-LRRK2 (wild-type, kinase-inactive mutant (K1906M), or FPD mutants). Rab10 phosphorylation was examined by P-tag SDS-PAGE followed by immunoblotting using an anti-HA antibody (Figure 2). 10 µg of proteins wer...

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Discussion

Here, we describe a facile and robust method of detecting Rab10 phosphorylation by LRRK2 at endogenous levels based on the P-tag methodology. Because the currently available antibody against phosphorylated Rab10 works only with overexpressed proteins¹⁵, the present method utilizing P-tag SDS-PAGE is the only way to assess endogenous levels of Rab10 phosphorylation. Moreover, the present method allows the estimation of the stoichiometry of Rab10 phosphorylation in cells. Because the P-tag methodolo...

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Materials

Name	Company	Catalog Number	Comments
Reagents
Dulbecco's phosphate-buffered saline (DPBS)	homemade		150 mM NaCl, 8 mM Na2HPO4-12H2O, 2.7 mM KCl, 1.5 mM KH2PO4 in MilliQ water and sterilized by autoclaving
Sodium chloride	Nacalai Tesque	31320-34
Sodium Disodium Hydrogenphosphate 12-Water	Wako	196-02835
Potassium chloride	Wako	163-03545
Potassium Dihydrogen Phosphate	Wako	169-04245
2.5% Trypsin (10X)	Sigma-Aldrich	T4549	Dilute 10-fold with sterile DPBS for preparing working solution
Dulbecco's modified Eagle medium (DMEM)	Wako	044-29765
Fetal bovine serum	BioWest	S1560	Heat-inactivated at 56 °C for 30 min
Penicillin-Streptomycin (100X)	Wako	168-23191
HEPES	Wako	342-01375
Sodium hydroxide	Wako	198-13765
Polyethylenimine HCl MAX, Linear, Mw 40,000 (PEI MAX 40000)	PolySciences, Inc.	24765-1	Stock solution was prepared in 20 mM HEPES-NaOH pH 7.0 at 1 mg/mL and the pH was then adjusted to 7.0 with NaOH
Dimethyl sulfoxide	Wako	045-28335
Tris	STAR	RSP-THA500G
Hydrochloric acid	Wako	080-01066
Polyoxyethylene(10) Octylphenyl Ether	Wako	160-24751	Equivalent to Triton X-100
Ethylene glycol-bis(2-aminoethylether)-N,N,N’,N’-tetraacetic acid (EGTA)	Wako	346-01312
Sodium orthovanadate(V)	Wako	198-09752
Sodium fluoride	Kanto Chemical	37174-20
β-Glycerophosphoric Acid Disodium Salt Pentahydrate	Nacalai Tesque	17103-82
Sodium pyrophosphate decahydrate	Kokusan Chemical	2113899
Microcystin-LR	Wako	136-12241
Sucrose	Wako	196-00015
Complete EDTA-free protease inhibitor cocktail	Roche	11873580001	Dissolve one tablet in 1 mL water, which can be stored at -20 °C for a month. Use it at 1:50 dilution for cell lysis
Pierce Coomassie (Bradford) Protein Assay Kit	Thermo Fisher Scientific	23200
Sodium dodecyl sulfate	Nacalai Tesque	31607-65
Glycerol	Wako	075-00616
Bromophenol blue	Wako	021-02911
β-mercaptoethanol	Kanto Chemical	25099-00
Ethanol	Wako	056-06967
Methanol	Wako	136-01837
Phosphate-binding tag acrylamide	Wako	AAL-107	P-tag acrylamide
40% (w/v) acrylamide solution	Nacalai Tesque	06119-45	Acrylamide:Bis = 29:1
Tetramethylethylenediamine (TEMED)	Nacalai Tesque	33401-72
Ammonium persulfate (APS)	Wako	016-08021	10% (w/v) solution was prepared by dissolving the powder of ammonium persulfate in MilliQ water
2-propanol	Wako	166-04831
Manganese chloride tetrahydrate	Sigma-Aldrich	M3634
Precision Plus Protein Prestained Standard	Bio-Rad	1610374, 1610373, 1610377	Molecular weight marker used in the protocol
WIDE-VIEW Prestained Protein Size Marker III	Wako	230-02461
Glycine	Nacalai Tesque	17109-64
Amersham Protran NC 0.45	GE Healthcare	10600007	Nitrocellulose membrane
Durapore Membrane Filter	EMD Millipore	GVHP00010	PVDF membrane
Filter Papers No.1	Advantec	00013600
Ponceau S	Nacalai Tesque	28322-72
Acetic acid	Wako	017-00251
Tween-20	Sigma-Aldrich	P1379	polyoxyethylenesorbitan monolaurate
Ethylenediaminetetraacetic acid (EDTA)	Wako	345-01865
Skim milk powder	Difco Laboratories	232100
Immunostar	Wako	291-55203	ECL solution (Normal sensitivity)
Immunostar LD	Wako	290-69904	ECL solution (High sensitivity)
CBB staining solution	homemade		1 g CBB R-250, 50% (v/v) methanol, 10% (v/v) acetic acid in 1 L of MilliQ water
CBB R-250	Wako	031-17922
CBB destaining solution	homemade		12% (v/v) methanol, 7% (v/v) acetic acid in 1 L MilliQ water
Name	Company	Catalog Number	Comments
Antibodies
anti-HA antibody	Sigma-Aldrich	11583816001	Used at 0.2 μg/mL for immunoblotting.
anti-Rab10 antibody	Cell Signaling Technology	#8127	Used at 1:1000 for immunoblotting. Specificity was confirmed by CRISPR KO in Ito et al., Biochem J, 2016.
anti-pSer935 antibody	Abcam	ab133450	Used at 1 μg/mL for immunoblotting.
anti-LRRK2 antibody	Abcam	ab133518	Used at 1 μg/mL for immunoblotting.
anti-α-tubulin antibody	Sigma-Aldrich	T9026	Used at 1 μg/mL for immunoblotting.
anti-GAPDH antibody	Santa-Cruz	sc-32233	Used at 0.02 μg/mL for immunoblotting.
Peroxidase AffiniPure Sheep Anti-Mouse IgG (H+L)	Jackson ImmunoResearch	515-035-003	Used at 0.16 μg/mL for immunoblotting.
Peroxidase AffiniPure Goat Anti-Rabbit IgG (H+L)	Jackson ImmunoResearch	111-035-003	Used at 0.16 μg/mL for immunoblotting.
Name	Company	Catalog Number	Comments
Inhibitors
GSK2578215A	MedChem Express	HY-13237	Stock solution was prepared in DMSO at 10 mM and stored at -80 °C
MLi-2	Provided by Dr Dario Alessi (University of Dundee)		Stock solution was prepared in DMSO at 10 mM and stored at -80 °C
Name	Company	Catalog Number	Comments
Plasmids
Rab10/pcDNA5 FRT TO HA	Provided by Dr Dario Alessi (University of Dundee)		This plasmid expresses amino-terminally HA-tagged human Rab10.
LRRK2 WT/p3xFLAG-CMV-10	Provided by Dr Takeshi Iwatsubo (University of Tokyo)		Ito et al., Biochemistry, 46: 1380–1388 (2007). This plasmid expresses amino-terminally 3xFLAG-tagged wild-type human LRRK2.
LRRK2 K1906M/p3xFLAG-CMV-10	Provided by Dr Takeshi Iwatsubo (University of Tokyo)		Ito et al., Biochemistry, 46: 1380–1388 (2007). This plasmid expresses amino-terminally 3xFLAG-tagged K1906M kinase-inactive mutant of human LRRK2.
LRRK2 N1437H/p3xFLAG-CMV-10			This paper. This plasmid expresses amino-terminally 3xFLAG-tagged N1437H FPD mutant of human LRRK2.
LRRK2 R1441C/p3xFLAG-CMV-10	Provided by Dr Takeshi Iwatsubo (University of Tokyo)		Kamikawaji et al., Biochemistry, 48: 10963–10975 (2013). This plasmid expresses amino-terminally 3xFLAG-tagged R1441C FPD mutant of human LRRK2.
LRRK2 R1441G/p3xFLAG-CMV-10	Provided by Dr Takeshi Iwatsubo (University of Tokyo)		Kamikawaji et al., Biochemistry, 48: 10963–10975 (2013). This plasmid expresses amino-terminally 3xFLAG-tagged R1441G FPD mutant of human LRRK2.
LRRK2 R1441H/p3xFLAG-CMV-10	Provided by Dr Takeshi Iwatsubo (University of Tokyo)		Kamikawaji et al., Biochemistry, 48: 10963–10975 (2013). This plasmid expresses amino-terminally 3xFLAG-tagged R1441H FPD mutant of human LRRK2.
LRRK2 R1441S/p3xFLAG-CMV-10			This paper. This plasmid expresses amino-terminally 3xFLAG-tagged R1441S FPD mutant of human LRRK2.
LRRK2 Y1699C/p3xFLAG-CMV-10	Provided by Dr Takeshi Iwatsubo (University of Tokyo)		Kamikawaji et al., Biochemistry, 48: 10963–10975 (2013). This plasmid expresses amino-terminally 3xFLAG-tagged Y1699C FPD mutant of human LRRK2.
LRRK2 G2019S/p3xFLAG-CMV-10	Provided by Dr Takeshi Iwatsubo (University of Tokyo)		Kamikawaji et al., Biochemistry, 48: 10963–10975 (2013). This plasmid expresses amino-terminally 3xFLAG-tagged G2019S FPD mutant of human LRRK2.
LRRK2 I2020T/p3xFLAG-CMV-10	Provided by Dr Takeshi Iwatsubo (University of Tokyo)		Kamikawaji et al., Biochemistry, 48: 10963–10975 (2013). This plasmid expresses amino-terminally 3xFLAG-tagged I2020T FPD mutant of human LRRK2.
Name	Company	Catalog Number	Comments
Equipments
CO2 incubator	Thermo Fisher Scientific	Forma Series II 3110 Water-Jacketed
Auto Pipette	Drummond	Pipet-Aid PA-400
Micropipette P10	Nichiryo	00-NPX2-10	0.5–10 μL
Micropipette P200	Nichiryo	00-NPX2-200	20–200 μL
Micropipette P1000	Nichiryo	00-NPX2-1000	100–1000 μL
Tips for micropipette P10	STAR	RST-481LCRST	Sterile
Tips for micropipette P200	FUKAEKASEI	1201-705YS	Sterile
Tips for micropipette P1000	STAR	RST-4810BRST	Sterile
5 mL disporsable pipette	Greiner	606180	Sterile
10 mL disporsable pipette	Greiner	607180	Sterile
25 mL disporsable pipette	Falcon	357535	Sterile
Hematocytometer	Sunlead Glass	A126	Improved Neubeuer
Microscope	Olympus	CKX53
10 cm dishes	Falcon	353003	For tissue culture
6-well plates	AGC Techno Glass	3810-006	For tissue culture
Vortex mixer	Scientific Industries	Vortex-Genie 2
Cell scrapers	Sumitomo Bakelite	MS-93100
1.5 mL tubes	STAR	RSV-MTT1.5
15 mL tubes	AGC Techno Glass	2323-015
50 mL tubes	AGC Techno Glass	2343-050
Centrifuges	TOMY	MX-307
96-well plates	Greiner	655061	Not for tissue culture
Plate reader	Molecular Devices	SpectraMax M2e
SDS–PAGE tanks	Nihon Eido	NA-1010
Transfer tanks	Nihon Eido	NA-1510B
Gel plates (notched)	Nihon Eido	NA-1000-1
Gel plates (plain)	Nihon Eido	NA-1000-2
Silicon spacers	Nihon Eido	NA-1000-16
17-well combs	Nihon Eido	Custom made
Binder clips	Nihon Eido	NA-1000-15
5 mL syringe	Terumo	SS-05SZ
21G	Terumo	NN-2138R
Power Station 1000 VC	ATTO	AE-8450	Power supply for SDS–PAGE and transfer
Large weighing boats	Ina Optika	AS-DL
Plastic containers	AS ONE	PS CASE No.4	10 x 80 x 50 mm
Rocking shaker	Titech	NR-10
Styrene foam box	generic		The internal dimensions should fit one transfer tank (200 x 250 x 250 mm).
ImageQuant LAS-4000	GE Healthcare		An imager equipped with a cooled CCD camera for detection of ECL