Consensus, controversies, and conundrums of P4-ATPases: The emerging face of eukaryotic lipid flippases

被引:4
|
作者
Duan, H. Diessel [1 ]
Li, Huilin [1 ]
机构
[1] Van Andel Inst, Dept Struct Biol, Grand Rapids, MI 49503 USA
基金
美国国家卫生研究院;
关键词
PHOSPHOLIPID FLIPPASE; REACTION CYCLE; ATPASE; TRANSPORT; MECHANISM; MEMBRANE; ASYMMETRY; MODEL; GENE; PUMP;
D O I
10.1016/j.jbc.2024.107387
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
The cryo-EM resolution revolution has heralded a new era in our understanding of eukaryotic lipid flippases with a rapidly growing number of high-resolution structures. Flippases belong to the P4 family of ATPases (type IV P-type ATPases) that largely follow the reaction cycle proposed for the more extensively studied cation-transporting P-type ATPases. However, unlike the canonical P-type ATPases, no flippase cargos are transported in the phosphorylation half-reaction. Instead of being released into the intracellular or extracellular milieu, lipid cargos are transported to their destination at the inner leaflet of the membrane. Recent flippase structures have revealed multiple conformational states during the lipid transport cycle. Nonetheless, critical conformational states capturing the lipid cargo "in transit" are still missing. In this review, we highlight the amazing structural advances of these lipid transporters, discuss various perspectives on catalytic and regulatory mechanisms in the literature, and shed light on future directions in further deciphering the detailed molecular mechanisms of lipid flipping.
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页数:14
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