Thermal Shift Assay for Characterizing the Stability of RNA Helicases and Their Interaction with Ligands.
Differential scanning fluorimetry
Melting temperature
RNA helicase
Thermal shift assay
Thermofluor
Thermostability
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
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