Literature DB >> 33201463

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

Emmanuel Saridakis1, Franck Coste2.   

Abstract

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.

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Keywords:  Differential scanning fluorimetry; Melting temperature; RNA helicase; Thermal shift assay; Thermofluor; Thermostability

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Year:  2021        PMID: 33201463     DOI: 10.1007/978-1-0716-0935-4_5

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  Cryo-EM structure of transcription termination factor Rho from Mycobacterium tuberculosis reveals bicyclomycin resistance mechanism.

Authors:  Emmanuel Saridakis; Rishi Vishwakarma; Josephine Lai-Kee-Him; Kevin Martin; Isabelle Simon; Martin Cohen-Gonsaud; Franck Coste; Patrick Bron; Emmanuel Margeat; Marc Boudvillain
Journal:  Commun Biol       Date:  2022-02-09
  1 in total

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