Clathrin-coated vesicles (CCVs) carry out receptor-mediated endocytosis at the plasma membrane, where they mediate the uptake of receptor bound nutrients, hormones and proteins destined for degradation. In the trans-Golgi network, CCVs are required biogenesis of lysosomes and secretory granules. The assembling unit, or clathrin triskelion, is composed of three heavy chains and three light chains. The polymerization of clathrin triskelions drives the formation of the lattice: thus clathrin self-assembly provides the mechanism for the receptor-concentrating function of clathrin-coated vesicles, leading to selective transport of any elements that can associate with the lattice. The structural analysis of the recombinant hub/LCb complex will lead to the molecular mechanism of clathrin self-assembly.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001209-20
Application #
6119588
Study Section
Project Start
1999-03-01
Project End
2000-04-14
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
20
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
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