A molecular toolbox for interrogation of membrane contact sites

被引:28
|
作者
Jing, Ji [1 ]
Liu, Gan [2 ]
Huang, Yun [3 ]
Zhou, Yubin [1 ]
机构
[1] Texas A&M Univ, Coll Med, Ctr Translat Canc Res, Inst Biosci & Technol, Houston, TX 77030 USA
[2] Univ Texas Austin, Cockrell Sch Engn, Austin, TX 78712 USA
[3] Texas A&M Univ, Coll Med, Ctr Epigenet & Dis Prevent, Inst Biosci & Technol, Houston, TX 77030 USA
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2020年 / 598卷 / 09期
关键词
Membrane contact sites; MCSs visualization; MCSs manipulation; Calcium homeostasis; lipid metabolism; organelle remodeling; fluorescence; optogenetics; REFLECTION FLUORESCENCE MICROSCOPY; ACTIVATES CRAC CHANNELS; ENDOPLASMIC-RETICULUM; PLASMA-MEMBRANE; OPTOGENETIC CONTROL; STIM PROTEINS; CA2+ SENSOR; IN-SITU; ER; MITOCHONDRIA;
D O I
10.1113/JP277761
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Membrane contact sites (MCSs) are specialized subcellular compartments formed by closely apposed membranes from two organelles. The intermembrane gap is separated by a distance ranging from 10 to 35 nm. MCSs are typically maintained through dynamic protein-protein and protein-lipid interactions. These intermembrane contact sites constitute important intracellular signalling hotspots to mediate a plethora of cellular processes, including calcium homeostasis, lipid metabolism, membrane biogenesis and organelle remodelling. In recent years, a series of genetically encoded probes and chemogenetic or optogenetic actuators have been invented to aid the visualization and interrogation of MCSs in both fixed and living cells. These molecular tools have greatly accelerated the pace of mechanistic dissection of membrane contact sites at the molecular level. In this review, we present an overview on the latest progress in this endeavour, and provide a general guide to the selection of methods and molecular tools for probing interorganellar membrane contact sites.
引用
收藏
页码:1725 / 1739
页数:15
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