Phospholipid-flipping activity of P4-ATPase drives membrane curvature

被引:46
|
作者
Takada, Naoto [1 ]
Naito, Tomoki [1 ]
Inoue, Takanari [2 ]
Nakayama, Kazuhisa [1 ]
Takatsu, Hiroyuki [1 ]
Shin, Hye-Won [1 ]
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto, Japan
[2] Johns Hopkins Univ, Dept Cell Biol, Sch Med, Ctr Cell Dynam, Baltimore, MD USA
来源
EMBO JOURNAL | 2018年 / 37卷 / 09期
关键词
BAR domain; curvature; flippase; lipid; plasma membrane; TRANS-GOLGI NETWORK; P-TYPE ATPASES; PLASMA-MEMBRANE; AMINOPHOSPHOLIPID TRANSLOCASE; TRANSBILAYER DISTRIBUTION; RECYCLING ENDOSOMES; LIPID ASYMMETRY; BAR DOMAINS; PHOSPHATIDYLSERINE; FLIPPASES;
D O I
10.15252/embj.201797705
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
P4-ATPases are phospholipid flippases that translocate phospholipids from the exoplasmic/luminal to the cytoplasmic leaflet of biological membranes. All P4-ATPases in yeast and some in other organisms are required for membrane trafficking; therefore, changes in the transbilayer lipid composition induced by flippases are thought to be crucial for membrane deformation. However, it is poorly understood whether the phospholipid-flipping activity of P4-ATPases can promote membrane deformation. In this study, we assessed membrane deformation induced by flippase activity via monitoring the extent of membrane tubulation using a system that allows inducible recruitment of Bin/amphiphysin/Rvs (BAR) domains to the plasma membrane (PM). Enhanced phosphatidylcholine-flippase activity at the PM due to expression of ATP10A, a member of the P4-ATPase family, promoted membrane tubulation upon recruitment of BAR domains to the PM. This is the important evidence that changes in the transbilayer lipid composition induced by P4-ATPases can deform biological membranes.
引用
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页数:14
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