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Newly-formed synaptic vesicles (SVs) are rapidly acidified by vacuolar adenosine triphosphatases (vATPases), generating a proton electrochemical gradient that drives neurotransmitter loading. Clathrin-mediated endocytosis is needed for the formation of new SVs, yet it is unclear when endocytosed vesicles acidify and refill at the synapse. Here, we isolated clathrin-coated vesicles (CCVs) from mouse brain to measure their acidification directly at the single vesicle level. We observed that the ATP-induced acidification of CCVs was strikingly reduced in comparison to SVs. Remarkably, when the coat was removed from CCVs, uncoated vesicles regained ATP-dependent acidification, demonstrating that CCVs contain the functional vATPase, yet its function is inhibited by the clathrin coat. Considering the known structures of the vATPase and clathrin coat, we propose a model in which the formation of the coat surrounds the vATPase and blocks its activity. Such inhibition is likely fundamental for the proper timing of SV refilling.

Original publication

DOI

10.7554/elife.32569

Type

Journal article

Journal

eLife

Publication Date

13/04/2018

Volume

7

Addresses

Department of Neurobiology, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.

Keywords

Brain, Synaptic Vesicles, Clathrin-Coated Vesicles, Animals, Mice, Vacuolar Proton-Translocating ATPases, Clathrin, Adenosine Triphosphate, Hydrolysis