4.6 Review Book Chapter

Regulation of Clathrin-Mediated Endocytosis

期刊

ANNUAL REVIEW OF BIOCHEMISTRY, VOL 87
卷 87, 期 -, 页码 871-896

出版社

ANNUAL REVIEWS
DOI: 10.1146/annurev-biochem-062917-012644

关键词

dynamin; endocytic accessory proteins; signaling; AP2; adaptor protein-2; evolution; endocytic checkpoint

资金

  1. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM073165, R01GM042455] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH061345] Funding Source: NIH RePORTER
  3. NIGMS NIH HHS [R01 GM042455, R01 GM073165] Funding Source: Medline
  4. NIMH NIH HHS [R01 MH061345, R37 MH061345] Funding Source: Medline

向作者/读者索取更多资源

Clathrin-mediated endocytosis (CME) is the major endocytic pathway in mammalian cells. It is responsible for the uptake of transmembrane receptors and transporters, for remodeling plasma membrane composition in response to environmental changes, and for regulating cell surface signaling. CME occurs via the assembly and maturation of clathrin-coated pits that concentrate cargo as they invaginate and pinch off to form clathrin-coated vesicles. In addition to the major coat proteins, clathrin triskelia and adaptor protein complexes, CME requires a myriad of endocytic accessory proteins and phosphatidylinositol lipids. CME is regulated at multiple steps-initiation, cargo selection, maturation, and fission-and is monitored by an endocytic checkpoint that induces disassembly of defective pits. Regulation occurs via posttranslational modifications, allosteric conformational changes, and isoform and splice-variant differences among components of the CME machinery, including the GTPase dynamin. This review summarizes recent findings on the regulation of CME and the evolution of this complex process.

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