Literature DB >> 33732775

A Mant-GDP Dissociation Assay to Compare the Guanine Nucleotide Binding Preference of Small GTPases.

Yuping Tan1, Qingxiang Sun1.   

Abstract

Small GTPases are cellular switches that are switched on when bound to GTP and switched off when bound to GDP. Different small GTPase proteins or those with mutations may bind to GTP or GDP with different relative affinities. However, small GTPases generally have very high affinities for guanine nucleotides, rendering it difficult to compare the relative binding affinities for GTP and GDP. Here we developed a method for comparing the relative binding strength of a protein to GTP and GDP using a mant-GDP dissociation assay, whereby the abilities of GTP and GDP to induce the dissociation of bound mant-GDP are compared. This equilibrium type assay is simple, economic, and much faster than obtaining each protein's affinity for GDP and GTP. The GDP/GTP preference value obtained is useful for comparing the relative GTP/GDP binding preferences of different GTPases or different mutants, even though it is not the real GDP/GTP affinity ratio (but rather an estimation of the ratio).
Copyright © 2021 The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  Binding; Dissociation; GTPase; Guanine nucleotide; Preference

Year:  2021        PMID: 33732775      PMCID: PMC7953247          DOI: 10.21769/BioProtoc.3886

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  16 in total

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Journal:  Biochemistry       Date:  1995-01-17       Impact factor: 3.162

9.  Purification of RanGDP, RanGTP, and RanGMPPNP by ion exchange chromatography.

Authors:  Niloufar Bibak; Rachelle M J Paul; Douglas M Freymann; Nabeel R Yaseen
Journal:  Anal Biochem       Date:  2004-10-01       Impact factor: 3.365

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Authors:  T Hiratsuka
Journal:  Biochim Biophys Acta       Date:  1983-02-15
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