Evidence map›Paper›PMID 42681196›Full record

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

A Dual-Color Electrophoretic Mobility Shift Assay to Examine RNA-Binding and RNA Chaperone Activity Simultaneously.

Tobias Schmidt

Abstract read
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In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Tobias SchmidtCancer Research UK Scotland Institute, Garscube Estate, Glasgow, UK. T.Schmidt@crukscotlandinstitute.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA-binding proteins that rearrange RNA structure often undergo complicated reaction pathways including multivalent interactions with itself and the RNA substrates. For detailed mechanistic understanding of these reactions, it is essential to get insight into the individual complexes formed during the reaction that can guide answering questions regarding sequence or stoichiometry of the reaction. Meanwhile high-resolution structural approaches allow discrimination of multiple conformations and complexes in a heterogeneous sample; however, these approaches are cost- and time-intensive and require extensive technical experience. Traditional electrophoretic mobility shift assays are cheap and require no specialized equipment, and can give valuable insight into reaction pathways resolving both RNA-RNA and protein-RNA interactions.In this chapter, I present an adaptation of a gel electrophoretic mobility shift assay using individually fluorescently labelled RNAs in a discontinuous gel system that can resolve protein-RNA and RNA-RNA complexes from a single reaction in the same gel. The method is applied and discussed based on the example of the RNA-unwinding activity of the RNA helicase eIF4A1 including a small molecule eIF4A1-modulator silvestrol. The example demonstrates the capacity of the assay to provide detailed mechanistic insight into rearrangement of RNA structure and protein-RNA interactions.

Indexed as

Electrophoretic Mobility Shift AssayMolecular ChaperonesRNARNA-Binding ProteinsEukaryotic Initiation Factor-4ANucleic Acid ConformationProtein BindingEukaryotic Initiation Factor-4AMolecular ChaperonesRNARNA-Binding ProteinsAnnealingRNA chaperoneRNA foldingStrand displacement

Identifiers

PMID42681196

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.