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Binding Affinity Measurement of Nuclear Export Signal Peptides to Their Exporter CRM1.
Fung, Ho Yee Joyce; Chook, Yuh Min.
Afiliação
  • Fung HYJ; Department of Pharmacology, UT Southwestern Medical Center, Dallas, TX, USA.
  • Chook YM; Department of Pharmacology, UT Southwestern Medical Center, Dallas, TX, USA. yuhmin.chook@utsouthwestern.edu.
Methods Mol Biol ; 2502: 245-256, 2022.
Article em En | MEDLINE | ID: mdl-35412243
ABSTRACT
CRM1 recognizes hundreds to thousands of protein cargoes by binding to the eight to fifteen residue-long nuclear export signals (NESs) within their polypeptide chains. Various assays to measure the binding affinity of NESs for CRM1 have been developed. CRM1 binds to NESs with a wide range of binding affinities, with dissociation constants that span from low nanomolar to tens of micromolar. An optimized binding affinity assay with improved throughput was recently developed to measure binding affinities of NES peptides for CRM1 in the presence of excess RanGTP. The assay can measure affinities, with multiple replicates, for up to seven different NES peptides per screening plate. Here, we present a protocol for the purification of the necessary proteins and for measuring CRM1-NES binding affinities.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Citoplasmáticos e Nucleares / Carioferinas / Sinais de Exportação Nuclear Idioma: En Revista: Methods Mol Biol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Citoplasmáticos e Nucleares / Carioferinas / Sinais de Exportação Nuclear Idioma: En Revista: Methods Mol Biol Ano de publicação: 2022 Tipo de documento: Article