Helical membrane protein folding, stability, and evolution

被引:525
作者
Popot, JL
Engelman, DM
机构
[1] Inst Biol Physicochim, CNRS, Lab Physicochim Mol Membranes Biol, UPR 9052, F-75005 Paris, France
[2] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[3] Chaire Int Rech Blaise Pascal Reg Ile France, Paris, France
关键词
membrane protein structure; two-stage model; helices; lipid bilayer; helix interactions;
D O I
10.1146/annurev.biochem.69.1.881
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Helical membrane protein folding and oligomerization can be usefully conceptualized as involving two energetically distinct stages-the formation and subsequent side-to-side association of independently stable transbilayer helices. The interactions of helices with the bilayer, with prosthetic groups, and with each other are examined in the context of recent evidence. We conclude that the two-stage concept remains useful as an approach to simplifying discussions of stability, as a framework for folding concepts, and as a basis for understanding membrane protein evolution.
引用
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页码:881 / 922
页数:42
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