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∆F508 CFTR interactome remodelling promotes rescue of cystic fibrosis

Academic Article
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Overview

authors

  • Pankow, S.
  • Bamberger, C.
  • Calzolari, D.
  • Martinez-Bartolome, S.
  • Lavallee-Adam, M.
  • Balch, William E.
  • Yates III, John

publication date

  • December 2015

journal

  • Nature  Journal

abstract

  • Deletion of phenylalanine 508 of the cystic fibrosis transmembrane conductance regulator (∆F508 CFTR) is the major cause of cystic fibrosis, one of the most common inherited childhood diseases. The mutated CFTR anion channel is not fully glycosylated and shows minimal activity in bronchial epithelial cells of patients with cystic fibrosis. Low temperature or inhibition of histone deacetylases can partly rescue ∆F508 CFTR cellular processing defects and function. A favourable change of ∆F508 CFTR protein-protein interactions was proposed as a mechanism of rescue; however, CFTR interactome dynamics during temperature shift and inhibition of histone deacetylases are unknown. Here we report the first comprehensive analysis of the CFTR and ∆F508 CFTR interactome and its dynamics during temperature shift and inhibition of histone deacetylases. By using a novel deep proteomic analysis method, we identify 638 individual high-confidence CFTR interactors and discover a ∆F508 deletion-specific interactome, which is extensively remodelled upon rescue. Detailed analysis of the interactome remodelling identifies key novel interactors, whose loss promote ∆F508 CFTR channel function in primary cystic fibrosis epithelia or which are critical for CFTR biogenesis. Our results demonstrate that global remodelling of ∆F508 CFTR interactions is crucial for rescue, and provide comprehensive insight into the molecular disease mechanisms of cystic fibrosis caused by deletion of F508.

subject areas

  • Bronchi
  • Cells, Cultured
  • Cystic Fibrosis
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Epithelial Cells
  • Gene Knockdown Techniques
  • Glycosylation
  • Histone Deacetylase Inhibitors
  • Histone Deacetylases
  • Humans
  • Mutant Proteins
  • Protein Folding
  • Protein Interaction Mapping
  • Protein Interaction Maps
  • Proteomics
  • RNA Interference
  • RNAi Therapeutics
  • Sequence Deletion
  • Temperature
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Identity

PubMed Central ID

  • PMC4826614

International Standard Serial Number (ISSN)

  • 0028-0836

Digital Object Identifier (DOI)

  • 10.1038/nature15729

PubMed ID

  • 26618866
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Additional Document Info

start page

  • 510

end page

  • 516

volume

  • 528

issue

  • 7583

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