期刊
SCIENCE
卷 328, 期 5983, 页码 1281-1284出版社
AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1188462
关键词
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资金
- MRC, UK
- MRC-LMB Ph.D. scholarship
- Human Frontiers Science Program Organization
- European Molecular Biology Organization
- MRC [MC_U105178795] Funding Source: UKRI
- Medical Research Council [MC_U105178795] Funding Source: researchfish
Clathrin-mediated endocytosis, the major pathway for ligand internalization into eukaryotic cells, is thought to be initiated by the clustering of clathrin and adaptors around receptors destined for internalization. However, here we report that the membrane-sculpting F-BAR domain-containing Fer/Cip4 homology domain-only proteins 1 and 2 (FCHo1/2) were required for plasma membrane clathrin-coated vesicle (CCV) budding and marked sites of CCV formation. Changes in FCHo1/2 expression levels correlated directly with numbers of CCV budding events, ligand endocytosis, and synaptic vesicle marker recycling. FCHo1/2 proteins bound specifically to the plasma membrane and recruited the scaffold proteins eps15 and intersectin, which in turn engaged the adaptor complex AP2. The FCHo F-BAR membrane-bending activity was required, leading to the proposal that FCHo1/2 sculpt the initial bud site and recruit the clathrin machinery for CCV formation.
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