ATPases: how an old dog learnt new tricks - structure and mechanism of lipid flippases

被引:27
作者
Lyons, Joseph A. [1 ]
Timcenko, Milena [1 ]
Dieudonne, Thibaud [1 ,2 ]
Lenoir, Guillaume [2 ]
Nissen, Poul [1 ]
机构
[1] Aarhus Univ, Danish Res Inst Translat Neurosci DANDRITE, Dept Mol Biol & Genet, Nord EMBL Partnership Mol Med, Aarhus, Denmark
[2] Univ Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, F-91198 Gif Sur Yvette, France
关键词
P-TYPE ATPASES; PHOSPHOLIPID FLIPPASE; TRANSPORT; EXPRESSION; IDENTIFICATION; TRANSLOCASE; CA2+-ATPASE; REMOVAL; CDC50A; DRS2P;
D O I
10.1016/j.sbi.2020.04.001
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
Type 4 P-type ATPases (P4-ATPases) are lipid flippases that drive the active, inward directed translocation (flip) of lipids in eukaryotic membranes. The resulting lipid asymmetry potentiates the membrane and is essential for a wide range of cellular processes such as vesicle biogenesis and trafficking and membrane protein regulation, whereas dissipation of lipid asymmetry is required in blood coagulation and apoptosis. Through recent advances in cryo-electron microscopy, several landmark structures of yeast and human lipid flippases have been reported, highlighting the similarities and differences they share with the cation transporting P-type ATPases. Here, we discuss the recent lipid flippase structures in the context of subunit architecture and organization, auto-regulation and lipid transport.
引用
收藏
页码:65 / 73
页数:9
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