Peripheral Protein Quality Control Removes Unfolded CFTR from the Plasma Membrane

Author:

Okiyoneda Tsukasa1,Barrière Hervé1,Bagdány Miklós1,Rabeh Wael M.1,Du Kai1,Höhfeld Jörg2,Young Jason C.3,Lukacs Gergely L.1

Affiliation:

1. Department of Physiology, and Groupe de Recherche Axé sur la Structure des Protéine (GRASP) McGill University, Montreal, Quebec H3G 1Y6, Canada.

2. Cell Biology Institute, University Bonn, D-53121 Bonn, Germany.

3. Department of Biochemistry, and Groupe de Recherche Axé sur la Structure des Protéine (GRASP) McGill University, Montreal, Quebec H3G 1Y6, Canada.

Abstract

Peripheral Quality Control Protein misfolding diseases often lead to the retention and degradation of important proteins within the endoplasmic reticulum (ER). Strategies to reduce the stringency of ER quality control that allow the proteins to carry on through the secretory pathway to reach their destination at the cell surface have shown some promise. Okiyoneda et al. (p. 805 , published online 1 July; see the Perspective by Hutt and Balch ) wanted to understand how, even if a protein reaches its destination, it may still be subjected to a second level of quality control and be cleared from the plasma membrane. Using functional small-interfering RNA screens in cells expressing the common cystic fibrosis mutation F508CFTR, the authors identified a pair of chaperones that promoted clearance of defective proteins from the plasma membrane. This peripheral quality-control step will also need to be overcome to increase the effectiveness of strategies to overcome protein misfolding disorders.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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