Evidence map›Paper›PMID 42862241›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2027

In Vitro Assay of Bacterial RNA Helicases Liquid-Liquid Phase Separation.

Johan Geiser, Martina Valentini

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Article in Methods in molecular biology (Clifton, N.J.), 2027. 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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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Johan GeiserDepartment of Microbiology and Molecular Medicine, University of Geneva, Geneva 4, Switzerland.
Martina ValentiniDepartment of Microbiology and Molecular Medicine, University of Geneva, Geneva 4, Switzerland. Martina.Valentini@unige.ch.ORCID http://orcid.org/0000-0002-1948-8339

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DEAD-box RNA helicases are widespread ATP-driven enzymes that reshape RNA structures and RNA-protein complexes during many steps of RNA metabolism. In bacteria, DEAD-box RNA helicases support cellular growth and responses to stress by contributing to ribosome biogenesis, RNA degradation, and translation initiation. Growing evidence indicates that several DEAD-box RNA helicases can also form liquid-liquid phase-separated condensates that concentrate RNA and partner proteins. This behavior adds a new layer of control to RNA regulation, although the molecular factors that promote or tune liquid-liquid phase separation (LLPS) are still unclear. Here, we describe an in vitro microscopy-based assay to characterize the LLPS behavior of bacterial DEAD-box RNA helicases. The protocol includes step-by-step procedures to evaluate condensate formation, salt sensitivity and dissolution, RNA dependency and specificity, and ATP effects. We further provide detailed instructions for quantitative analysis of microscope images, including size and assessment of protein enrichment within condensates. Altogether, this workflow enables systematic dissection of key physicochemical parameters governing DEAD-box helicase LLPS and provides a standardised framework for comparative studies across bacterial DEAD-box proteins or variants.

Indexed as

BacteriaBacterial ProteinsDEAD-box RNA HelicasesRNA HelicasesAdenosine TriphosphatePhase SeparationAdenosine TriphosphateBacterial ProteinsDEAD-box RNA HelicasesRNA HelicasesDEAD-box proteinsImage analysisIntrinsically disordered region (IDR)Liquid–liquid phase separation (LLPS)MicroscopyRNA helicase

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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 OpenQuestion graph.