Membrane-integration Characteristics of Two ABC Transporters, CFTR and P-glycoprotein
Journal of Molecular Biology 387(5): 1153-1164
Article 2009 English
Authors
KE
Karl Enquist
MF
Mawritz Fransson
CB
Carolina Boekel
Abstract
1 min read
To what extent do corresponding transmembrane helices in related integral membrane proteins have different membrane-insertion characteristics? Here, we compare, side-by-side, the membrane insertion characteristics of the 12 transmembrane helices in the adenosine triphosphate-binding cassette (ABC) transporters, P-glycoprotein (P-gp) and the cystic fibrosis transmembrane conductance regulator (CFTR). Our results show that 10 of the 12 CFTR transmembrane segments can insert independently into the ER membrane. In contrast, only three of the P-gp transmembrane segments are independently stable in the membrane, while the majority depend on the presence of neighboring loops and/or transmembrane segments for efficient insertion. Membrane-insertion characteristics can thus vary widely between related proteins.
Élodie Lainey, Marie Sébert, Sylvain Thépot, Marie Scoazec, Cyrielle Bouteloup, Carole Leroy, Stéphane de Botton, Lorenzo Galluzzi, Pierre Fenaux, Guido Guido Kroemer
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