PDZD8 mediates a Rab7-dependent interaction of the ER with late endosomes and lysosomes

被引:56
|
作者
Guillen-Samander, Andres [1 ,2 ,3 ,4 ]
Bian, Xin [1 ,2 ,3 ,4 ]
De Camilli, Pietro [1 ,2 ,3 ,4 ,5 ]
机构
[1] Yale Univ, Sch Med, HHMI, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Neurosci, New Haven, CT 06510 USA
[3] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06510 USA
[4] Yale Univ, Sch Med, Program Cellular Neurosci Neurodegenerat & Repair, New Haven, CT 06510 USA
[5] Yale Univ, Sch Med, Kavli Inst Neurosci, New Haven, CT 06510 USA
关键词
SMP domain; lipid-transfer protein; membrane contact sites; MEMBRANE CONTACT SITES; LIPID-BINDING PROTEINS; MITOCHONDRIA; METABOLISM; VACUOLES;
D O I
10.1073/pnas.1913509116
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Contacts between the endoplasmic reticulum (ER) and other membranes are hot spots for protein-mediated lipid transport between the 2 adjacent bilayers. Compiling a molecular inventory of lipid transport proteins present at these sites is a premise to the elucidation of their function. Here we show that PDZD8, an intrinsic membrane protein of the ER with a lipid transport module of the SMP domain family, concentrates at contacts between the ER and late endosomes/lysosomes, where it interacts with GTP-Rab7. These findings suggest that PDZD8 may cooperate with other proteins that function at the ER-endo/lysosome interface in coordinating endocytic flow with lipid transport between endocytic membranes and the ER.
引用
收藏
页码:22619 / 22623
页数:5
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