Abstract
Clathrin-coated vesicles isolated from calf brain contain an ATP-dependent proton pump. Proton movement was monitored by measuring [14C]methylamine distribution. Addition of Mg2+ and ATP to coated vesicles equilibrated with [14C]methylamine resulted in the generation of a 4- to 5-fold concentration gradient, corresponding to a delta pH of 0.6-0.7 units between the medium and the acidic inside of the coated vesicles. ATP-dependent [14C]methylamine uptake was abolished by the proton ionophore carbonylcyanide p-trifluoromethoxyphenylhydrazone (FCCP) and partially inhibited by the carboxyl reagent N,N'-dicyclohexylcarbodiimide but was unaffected by the Na+, K+-ATPase inhibitors strophanthidin (100 microM) and vanadate (10 microM) and the mitochondrial ATPase inhibitors oligomycin (10 microgram/ml) and aurovertin (1 microgram/ml). GTP, but not the nonhydrolyzable analog 5'-adenylyl imidodiphosphate, could support [14C]methylamine uptake. Dissipation of the membrane potential with K+ and valinomycin resulted in stimulation of [14C]methylamine uptake, whereas both FCCP and valinomycin stimulated the strophanthidin-resistant ATPase activity. These results are consistent with the existence of an electrogenic, ATP-dependent proton pump in clathrin-coated vesicles. This proton pump may play a role in the acidification events that are essential in receptor-mediated endocytosis.
MeSH Terms
Adenosine Triphosphatases/analysis
Animals
Brain/enzymology,ultrastructure
Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone/pharmacology
Cattle
Clathrin
Coated Pits, Cell-Membrane/enzymology
Endosomes/enzymology
Magnesium/metabolism
Membrane Potentials/drug effects
Membrane Proteins
Methylamines/metabolism
Potassium/pharmacology
Proton-Translocating ATPases
Valinomycin/pharmacology
Chemicals
Clathrin
Membrane Proteins
Methylamines
Valinomycin
Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone
methylamine
Adenosine Triphosphatases
Proton-Translocating ATPases
Magnesium
Potassium
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Forgac M
Cantley L
Wiedenmann B
Altstiel L
Branton D
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