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. 1978 Sep;75(9):4394–4398. doi: 10.1073/pnas.75.9.4394

Coated vesicles: characterization, selective dissociation, and reassembly.

M P Woodward, T F Roth
PMCID: PMC336121  PMID: 30086

Abstract

Sodium dodecyl sulfate/polyacrylamide gels of coated vesicles from porcine brain (mean 76% coated vesicles) show three major proteins (180,000, 125,000, and 55,000 daltons) that account for 73% of the total protein. Preparations consisting predominantly of coats (65%) have less of the 55,000-dalton protein. Clathrin (180,000 daltons) comprises 40% of the protein of a coated vesicle. Conditions of 2 M urea, 0.25 M MgCl2, or pH 7.5 disrupt the coat and solubilize clathrin. Solubilized clathrin reforms coat structures after dilution of urea or MgCl2. High-pH-solubilized clathrin reassembles after dialysis against buffer at pH 6.5 containing dithiothreitol (5 mM). Reassembled coats are predominantly clathrin.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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