Evidence map›Paper›PMID 42681521›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Assay for In-Vitro Arginine Methylation of RNA Binding Proteins Followed by RNA Binding.

Sakshi Dewasthale, Gayatri Mohanan, Purusharth I Rajyaguru

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Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Sakshi DewasthaleDepartment of Biochemistry, Indian Institute of Science, Bangalore, India.
Gayatri MohananDepartment of Biochemistry, Indian Institute of Science, Bangalore, India.
Purusharth I RajyaguruDepartment of Biochemistry, Indian Institute of Science, Bangalore, India. rajyaguru@iisc.ac.in.ORCID http://orcid.org/0000-0003-3794-418X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Arginine methylation is a prevalent post-translational modification that plays a critical role in regulating the function of RNA-binding proteins [RBPs]. RBPs are the largest class of arginine methylated proteins. Catalyzed by protein arginine methyltransferases [PRMTs], this modification influences RNA recognition, binding affinity, and the formation of RNA-protein complexes. This impacts diverse cellular processes such as RNA splicing, transport, stability, and translation. Arginine methylation of RGG motifs modulates RBP behavior, with implications for normal physiology and disease states, including neurodegeneration, cancer, and immune disorders. In vitro methylation assays combined with RNA binding studies offer a powerful approach to elucidate how arginine methylation affects RNA-protein interactions. These techniques allow precise manipulation of methylation states and controlled assessment of binding dynamics, providing mechanistic insights into regulatory pathways. The protocols described in this chapter outline methods for recombinant protein expression, enzymatic methylation, and RNA binding assays, offering adaptable tools for researchers studying the functional consequences of arginine methylation in RNA biology. Together, these methodologies provide a framework to explore the interplay between post-translational modifications and RNA regulation, deepening our understanding of cellular processes.

Indexed as

ArginineRNARNA-Binding ProteinsHumansMethylationProtein-Arginine N-MethyltransferasesProtein BindingProtein Processing, Post-TranslationalArginineProtein-Arginine N-MethyltransferasesRNARNA-Binding ProteinsArginine methylationRGG-motifRNA-bindingRNA-protein interaction

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.