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Peptide binding consensus of the NHE‐RF‐PDZ1 domain matches the C‐terminal sequence of cystic fibrosis transmembrane conductance regulator (CFTR)

Peptide binding consensus of the NHE‐RF‐PDZ1 domain matches the C‐terminal sequence of cystic... The Na+‐H+ exchanger regulatory factor (NHE‐RF) is a cytoplasmic phosphoprotein that was first found to be involved in protein kinase A mediated regulation of ion transport. NHE‐RF contains two distinct protein interaction PDZ domains: NHE‐RF‐PDZ1 and NHE‐RF‐PDZ2. However, their binding partners are currently unknown. Because PDZ domains usually bind to specific short linear C‐terminal sequences, we have carried out affinity selection of random peptides for specific sequences that interact with the NHE‐RF PDZ domains and found that NHE‐RF‐PDZ1 is capable of binding to the CFTR C‐terminus. The specific and tight association suggests a potential regulatory role of NHE‐RF in cystic fibrosis transmembrane conductance regulator (CFTR) function. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Febs Letters Wiley

Peptide binding consensus of the NHE‐RF‐PDZ1 domain matches the C‐terminal sequence of cystic fibrosis transmembrane conductance regulator (CFTR)

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References (17)

Publisher
Wiley
Copyright
© 2015 Federation of European Biochemical Societies
eISSN
1873-3468
DOI
10.1016/S0014-5793(98)00402-5
Publisher site
See Article on Publisher Site

Abstract

The Na+‐H+ exchanger regulatory factor (NHE‐RF) is a cytoplasmic phosphoprotein that was first found to be involved in protein kinase A mediated regulation of ion transport. NHE‐RF contains two distinct protein interaction PDZ domains: NHE‐RF‐PDZ1 and NHE‐RF‐PDZ2. However, their binding partners are currently unknown. Because PDZ domains usually bind to specific short linear C‐terminal sequences, we have carried out affinity selection of random peptides for specific sequences that interact with the NHE‐RF PDZ domains and found that NHE‐RF‐PDZ1 is capable of binding to the CFTR C‐terminus. The specific and tight association suggests a potential regulatory role of NHE‐RF in cystic fibrosis transmembrane conductance regulator (CFTR) function.

Journal

Febs LettersWiley

Published: May 1, 1998

Keywords: ; ; ;

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