A novel adaptor-related protein complex

被引:207
作者
Simpson, F
Bright, NA
West, MA
Newman, LS
Darnell, RB
Robinson, MS
机构
[1] UNIV CAMBRIDGE, DEPT CLIN BIOCHEM, CAMBRIDGE CB2 2QR, ENGLAND
[2] ROCKEFELLER UNIV, MOLEC NEUROONCOL LAB, NEW YORK, NY 10021 USA
基金
英国惠康基金;
关键词
D O I
10.1083/jcb.133.4.749
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Coat proteins are required for the budding of the transport vesicles that mediate membrane traffic pathways, but for many pathways such proteins have not yet been identified. We have raised antibodies against p47, a homologue of the medium chains of the adaptor complexes of clathrin-coated vesicles (Pevsner, J., W. Volknandt, B.R. Wong, and R.H. Scheller. 1994, Gene (Amst.). 146:279-283), to determine whether this protein might be a component of a new type of coat. p47 coimmunoprecipitates with three other proteins: two unknown proteins of 160 and 25 kD, and beta-NAP, a homologue of the beta/beta'-adaptins, indicating that it is a subunit of an adaptor-like heterotetrameric complex. However, p47 is not enriched in preparations of clathrin-coated vesicles. Recruitment of the p47-containing complex onto cell membranes is stimulated by GTP gamma S and blocked by brefeldin A, indicating that, like other coat proteins, its membrane association is regulated by an ARF. The newly recruited complex is localized to non-clathrin-coated buds and vesicles associated with the TGN. Endogenous complex in primary cultures of neuronal cells is also localized to the TGN, and in addition, some complex is associated with the plasma membrane. These results indicate that the complex is a component of a novel type of coat that facilitates the budding of vesicles from the TGN, possibly for transporting newly synthesized proteins to the plasma membrane.
引用
收藏
页码:749 / 760
页数:12
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