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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Proximity ligation assay is a very useful technique to localize and quantify arginine methylation of a given protein when the modified arginine residue is unknown and/or if no specific antibody is available.

Abstract

Arginine methylation is emerging as a key post-translational modification involved in a large range of biological processes. Its study in tissue is often limited by the lack of a specific antibody recognizing the target arginine residue. Proximity ligation assay (PLA) was originally developed to study protein/protein interactions. Here, we describe in detail a PLA protocol dedicated to the detection of arginine methylation that we applied to the glucocorticoid receptor (GR). Having previously shown that PRMT5 dimethylates GRs in cells, we used PLA with a pan symmetrical dimethyl antibody and an anti-GR antibody to measure GR methylation in breast tumors. We demonstrate that PLA offers a unique approach to measure arginine methylation of a target protein, even when the site of methylation has not been identified. This technique could be extended to other post-translational modifications where effective pan antibodies are available. Hence, we detail the PLA technology used to detect arginine methylation in fixed tissue using GR as an example.

Introduction

Arginine methylation by protein arginine methyltransferases (PRMTs) is an abundant post-translational modification (PTM) involved in numerous biological processes. PRMTs catalyze the transfer of methyl groups from the S-adenosyl methionine to arginine residues. The PRMT family comprises nine members classified according to the type of methylation they perform. All members perform monomethylation (MMA). Type 1 (PRMT1, 2, 3, 4, 6, and 8) PRMTs catalyze asymmetrical dimethylation (ADMA), whereas type 2 (PRMT5 and 9) catalyze symmetrical dimethylation (SDMA), and type 3 (PRMT7) only generate MMA1. By methylating numerous substrates, the different P....

Protocol

Written informed consent was obtained from each patient. The study protocol was approved by the institutional ethics committee of the Cancer Research Center of Lyon.

1. Choice of the antibodies

  1. Use primary antibodies validated by IHC or immunofluorescence (IF).
    ​NOTE: The primary antibodies selected for the study are crucial to the success of PLA and more particularly in fixed tissue. Using an antibody validated by IHC or IF will increase the success r.......

Representative Results

Using the procedure described above, it is possible to detect and quantify the methylation of a protein of interest. Here, we show the example of the methylation of GR by PRMT5. The antibodies and the experimental conditions for PLA were previously applied to cells10. Briefly, primary antibodies targeting GR and SDMA are recognized by proximity probes conjugated with complementary oligonucleotides. Then, the hybridization of a circular DNA probe occurs when the proteins are in close proximity. Sub.......

Discussion

Arginine methylation, like other PTMs, contributes to the fine regulation of protein functions. However, its impact is underestimated due to the difficulty in assessing these modifications, primarily because of a lack of tools. This is particularly true when studying methylation in vivo, where the only way to measure arginine methylation is to possess specific antibodies recognizing the methylated residue of the protein of interest. This clearly constitutes a limitation as the methylated arginine residue must be.......

Acknowledgements

We would like to thank B. Manship for proofreading the manuscript. We acknowledge Laura Francols, Clémentine Le Nevé, Research pathology platform (CRCL) for technical help. Figure 1 was created using Servier Medical Art. This study was supported by the Ligue Inter-régionale contre le Cancer and the Association: 'Le Cancer du sein, parlons-en.'

....

Materials

NameCompanyCatalog NumberComments
Adhesion slides TOMO 90°, x100VWR631-1239
anti-GR antibody (mouse)Santa Cruzsc393232
anti-GR antibody (mouse)santa cruzsc393232
anti-PRMT5 antibody (rabbit)Merck07-405
anti-SDMA antibody (rabbit)CST13222
Automate d'inclusionLeicaASP 6025Paraffin infiltration and block preparation
Autostainer XLLeicaST5010Autostainer
Cassettes Q path macrostar III  x1500VWR720-2233
CC1Roche5279801001
Citrate Buffer pH 6 10x, 100 mLMMFF/T0050
Dako antibody diluentDako AgilentS202230-2antibody diluent
Discovery ChromoMap Diaminobenzidine (DAB) kitRoche760-159Diaminobenzidine (DAB) kit
Discovery WashRoche7311079001
Duolink insitu  PLA probe anti-mouse minusSigma-AldrichDUO92004PLA  kit (probe anti-rabbit minus)
Duolink insitu detection reagents brightfieldSigma-AldrichDUO92012PLA  kit (in situ detection reagents)
Duolink insitu PLA probe anti-rabbit plusSigma-AldrichDUO92002PLA  kit (probe anti-rabbit plus)
Duolink insitu wash buffer brightfieldSigma-AldrichDUO82047PLA  kit (in situ wash buffer)
Ethanol 96% VOL TECHNISOLV, 5 LVWR83804.360
Ethanol absolute ≥99.8%, AnalaR NORMAPUR ACS,  5 LVWR20821.365
EZ Prep 10xRoche5279771001
Formol, ready to use, 5 LMMFF/40877-36Formalin
Fully automated glass coverslipperLeicaCV5030automated coverslipper
Glass coverslips 24 x 40Dutscher100037
HematoxylinVentana760-2021
IHC instrumentRocheDISCOVERY XTAutomation of IHC
LCSRoche5264839001
MicrotomeThermo ScientificMicrom HM340ECutting of the tissues including in blocks
Mounting Medium PertexHistolab00801-FR
PAP Pen for immunostainingSigma-AldrichZ672548-1EA
Paraffin Wax tek III, 4 x 2, 5 kgSakura4511
Pasteur Disposable PipettesFisher Scientific12583237
PBS Buffer 10x, 100 mLMMFF/T0020
Reaction Buffer 10xRoche5353955001
Ribo Wash 10xRoche5266262001
RiboCC1Roche5266297001
Secondary antibody anti-mouseAbcamab133469
Secondary antibody OmniMap anti-rabbit HRPRoche760-4311
Tissue Embedding centerMMFEC 350
Xylene (mixture of isomers) ≥98.5%, AnalaR NORMAPUR ACS, 5 LVWR28975.360
Zeiss Axio Imager M2 microscopeupright bright-field microscope

References

  1. Blanc, R. S., Richard, S. Arginine methylation: The coming of age. Molecular Cell. 65 (1), 8-24 (2017).
  2. Malbeteau, L., et al. How protein methylation regulates steroid receptor function. Endocrine Reviews. 43

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