GRASP55, a second mammalian GRASP protein involved in the stacking of Golgi cisternae in a cell-free system

被引:271
作者
Shorter, J
Watson, R
Giannakou, ME
Clarke, M
Warren, G
Barr, FA
机构
[1] Univ Glasgow, IBLS, Div Biochem & Mol Biol, Glasgow G12 8QQ, Lanark, Scotland
[2] Imperial Canc Res Fund, Cell Biol Lab, London WC2A 3PX, England
基金
英国惠康基金;
关键词
cisternae; GM130; Golgi; GRASP65; stacking;
D O I
10.1093/emboj/18.18.4949
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
We have identified a 55 kDa protein, named GRASP55 (Golgi reassembly stacking protein of 55 kDa), as a component of the Golgi stacking machinery. GRASP55 is homologous to GRASP65, an N-ethylmaleimide-sensitive membrane protein required for the stacking of Golgi cisternae in a cell-free system. GRASP65 exists in a complex with the vesicle docking protein receptor GM130 to which it binds directly, and the membrane tethering protein p115, which also functions in the stacking of Golgi cisternae, GRASP55 binding to GM130, could not be detected using biochemical methods, although a weak interaction was detected with the yeast two-hybrid system. Cryo-electron microscopy revealed that GRASP65, like GM130, is present on the cis-Golgi, while GRASP55 is on the medial-Golgi. Recombinant GRASP55 and antibodies to the protein black the stacking of Golgi cisternae, which is similar to the observations made for GRASP65, These results demonstrate that GRASP55 and GRASP65 function in the stacking of Golgi cisternae.
引用
收藏
页码:4949 / 4960
页数:12
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