Article
VCP/p97 AAA-ATPase does not interact with the endogenous wild-type cystic fibrosis transmembrane conductance regulator.
American journal of respiratory cell and molecular biology - 1 Jun 2007
Goldstein Rebecca F, Niraj Ashutosh, Sanderson Todd P, Wilson Landon S, Rab Andras, Kim Helen, Bebok Zsuzsa, Collawn James F
Abstract excerpt
The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel that is defective in cystic fibrosis. The most common mutation, DeltaF508 CFTR, is retained in the endoplasmic reticulum, retrotranslocated into the cytosol, and degraded by the proteasome. In a proteomics screen to identify DeltaF508 CFTR interacting proteins, we found that valosin-containing protein (VCP)/p97, a Type II AAA...
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