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En bloc incorporation of coatomer subunits during the assembly of COP-coated vesicles.

ABSTRACT: The cDNA encoding epsilon-COP, the 36-kD subunit of coatomer, was cloned from a bovine liver cDNA library and sequenced. Immunoblotting with an anti-epsilon-COP antibody showed that epsilon-COP exists in COP-coated vesicles as well as in the cytosolic coatomer. Using the cloned cDNA, recombinant His6- tagged epsilon-COP was overexpressed in cultured Chinese hamster ovary (CHO) cells, from which metabolically radiolabeled coatomer was purified by taking advantage of the His6 tag. Radiolabeled coatomer was employed to establish that all the subunits of the coatomer enter coated vesicles as an intact unit.

SUBMITTER: Hara-Kuge S

PROVIDER: S-EPMC2119964 | biostudies-other | 1994 Mar

REPOSITORIES: biostudies-other

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En bloc incorporation of coatomer subunits during the assembly of COP-coated vesicles.

Hara-Kuge S S Kuge O O Orci L L Amherdt M M Ravazzola M M Wieland F T FT Rothman J E JE

The Journal of cell biology 19940301 6

The cDNA encoding epsilon-COP, the 36-kD subunit of coatomer, was cloned from a bovine liver cDNA library and sequenced. Immunoblotting with an anti-epsilon-COP antibody showed that epsilon-COP exists in COP-coated vesicles as well as in the cytosolic coatomer. Using the cloned cDNA, recombinant His6- tagged epsilon-COP was overexpressed in cultured Chinese hamster ovary (CHO) cells, from which metabolically radiolabeled coatomer was purified by taking advantage of the His6 tag. Radiolabeled coa ...[more]

PMID: 8132710

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A genome-wide analysis of coatomer protein (COP) subunits of apicomplexan parasites and their evolutionary relationships.

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A major transmembrane protein of Golgi-derived COPI-coated vesicles involved in coatomer binding.

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