Thermal Shift Assay for Characterizing the Stability of RNA Helicases and Their Interaction with Ligands.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2021
Historique:
entrez: 17 11 2020
pubmed: 18 11 2020
medline: 1 4 2021
Statut: ppublish

Résumé

Thermofluor or thermal shift assay is an easily implementable, high-throughput method for assessing the thermostability of proteins and the influence of various ligands on that stability. It is particularly useful for the assaying of ligands that may stabilize oligomeric helicases, which rely on both substrates (oligonucleotides) and nucleotide cofactors (ATP analogues) for their stability in a functional state. In this chapter, we describe the rationale and present a basic protocol for the use of this technique. Multi-ligand screening is also discussed via a worked example of the stabilization of a hexameric RNA helicase, a target protein for structural studies in our laboratories.

Identifiants

pubmed: 33201463
doi: 10.1007/978-1-0716-0935-4_5
doi:

Substances chimiques

Bacterial Proteins 0
Rho Factor 0
RNA Helicases EC 3.6.4.13

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

73-85

Auteurs

Emmanuel Saridakis (E)

Laboratory of Structural and Supramolecular Chemistry, Institute of Nanoscience and Nanotechnology, National Centre for Scientific Research "DEMOKRITOS", Athens, Greece. e.saridakis@inn.demokritos.gr.

Franck Coste (F)

Centre de Biophysique Moléculaire, CNRS UPR4301, Orléans Cedex 2, France.

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Classifications MeSH