Literature DB >> 35412243

Binding Affinity Measurement of Nuclear Export Signal Peptides to Their Exporter CRM1.

Ho Yee Joyce Fung1, Yuh Min Chook2.   

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.
© 2022. Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Binding affinity; CRM1; Fluorescence polarization; NES; Nuclear export signals; XPO1

Mesh:

Substances:

Year:  2022        PMID: 35412243     DOI: 10.1007/978-1-0716-2337-4_16

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


  13 in total

1.  An allosteric mechanism to displace nuclear export cargo from CRM1 and RanGTP by RanBP1.

Authors:  Masako Koyama; Yoshiyuki Matsuura
Journal:  EMBO J       Date:  2010-05-18       Impact factor: 11.598

2.  NES consensus redefined by structures of PKI-type and Rev-type nuclear export signals bound to CRM1.

Authors:  Thomas Güttler; Tobias Madl; Piotr Neumann; Danilo Deichsel; Lorenzo Corsini; Thomas Monecke; Ralf Ficner; Michael Sattler; Dirk Görlich
Journal:  Nat Struct Mol Biol       Date:  2010-10-24       Impact factor: 15.369

3.  RanGTP-regulated interactions of CRM1 with nucleoporins and a shuttling DEAD-box helicase.

Authors:  P Askjaer; A Bachi; M Wilm; F R Bischoff; D L Weeks; V Ogniewski; M Ohno; C Niehrs; J Kjems; I W Mattaj; M Fornerod
Journal:  Mol Cell Biol       Date:  1999-09       Impact factor: 4.272

4.  Structural basis for cooperativity of CRM1 export complex formation.

Authors:  Thomas Monecke; David Haselbach; Béla Voß; Andreas Russek; Piotr Neumann; Emma Thomson; Ed Hurt; Ulrich Zachariae; Holger Stark; Helmut Grubmüller; Achim Dickmanns; Ralf Ficner
Journal:  Proc Natl Acad Sci U S A       Date:  2012-12-31       Impact factor: 11.205

5.  Architecture of CRM1/Exportin1 suggests how cooperativity is achieved during formation of a nuclear export complex.

Authors:  Carlo Petosa; Guy Schoehn; Peter Askjaer; Ulrike Bauer; Martine Moulin; Ulrich Steuerwald; Montserrat Soler-López; Florence Baudin; Iain W Mattaj; Christoph W Müller
Journal:  Mol Cell       Date:  2004-12-03       Impact factor: 17.970

6.  Supraphysiological nuclear export signals bind CRM1 independently of RanGTP and arrest at Nup358.

Authors:  Dieuwke Engelsma; Rafael Bernad; Jero Calafat; Maarten Fornerod
Journal:  EMBO J       Date:  2004-08-26       Impact factor: 11.598

7.  The specificity of the CRM1-Rev nuclear export signal interaction is mediated by RanGTP.

Authors:  P Askjaer; T H Jensen; J Nilsson; L Englmeier; J Kjems
Journal:  J Biol Chem       Date:  1998-12-11       Impact factor: 5.157

8.  CRM1-mediated recycling of snurportin 1 to the cytoplasm.

Authors:  E Paraskeva; E Izaurralde; F R Bischoff; J Huber; U Kutay; E Hartmann; R Lührmann; D Görlich
Journal:  J Cell Biol       Date:  1999-04-19       Impact factor: 10.539

9.  Nuclear export receptor CRM1 recognizes diverse conformations in nuclear export signals.

Authors:  Ho Yee Joyce Fung; Szu-Chin Fu; Yuh Min Chook
Journal:  Elife       Date:  2017-03-10       Impact factor: 8.140

10.  Correlation of CRM1-NES affinity with nuclear export activity.

Authors:  Szu-Chin Fu; Ho Yee Joyce Fung; Tolga Cağatay; Jordan Baumhardt; Yuh Min Chook
Journal:  Mol Biol Cell       Date:  2018-06-21       Impact factor: 4.138

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