Isolation and reconstitution of the clathrin-coated vesicle proton translocating complex

J Biol Chem. 1986 Feb 25;261(6):2492-5.

Abstract

Clathrin-coated vesicles contain a proton translocating ATPase which is insensitive to azide but inhibited by N-ethylmaleimide. The ATP hydrolytic subunit of this proton pump has been solubilized, partially purified, and reconstituted into H+-ATPase-depleted coated vesicle membranes (Xie, X.-S., Stone, D.K., and Racker, E. (1984) J. Biol. Chem. 259, 11676-11678). In this communication we report that the entire proton transporting complex has been solubilized and purified 200-fold. The complex, when reconstituted into brain lipid liposomes, catalyzes azide-resistant, N-ethylmaleimide-sensitive H+ transport manifested as both generation of a pH gradient and an electrical gradient. The complex has an apparent molecular mass of 530 kDa.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Brain / enzymology
  • Brain / ultrastructure
  • Cattle
  • Coated Pits, Cell-Membrane / enzymology*
  • Electrophoresis, Polyacrylamide Gel
  • Endosomes / enzymology*
  • Ethylmaleimide / pharmacology
  • Molecular Weight
  • Proton-Translocating ATPases / isolation & purification*

Substances

  • Proton-Translocating ATPases
  • Ethylmaleimide