Ion transport and regulation in a synaptic vesicle glutamate transporter

Author:

Li Fei12ORCID,Eriksen Jacob2ORCID,Finer-Moore Janet1,Chang Roger23,Nguyen Phuong1,Bowen Alisa1ORCID,Myasnikov Alexander1ORCID,Yu Zanlin1ORCID,Bulkley David1ORCID,Cheng Yifan14ORCID,Edwards Robert H.2ORCID,Stroud Robert M.1ORCID

Affiliation:

1. Department of Biochemistry and Biophysics, University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA.

2. Departments of Neurology and Physiology, UCSF School of Medicine, San Francisco, CA, USA.

3. Graduate Program in Biomedical Sciences, UCSF, San Francisco, CA, USA.

4. Howard Hughes Medical Institute, UCSF, San Francisco, CA, USA.

Abstract

Transport dependent on context Transporter proteins move substrates across a membrane, often coupling this activity to cellular ion concentration gradients. For neurotransmitter transporters, which reside in synaptic vesicles that fuse with the plasma membrane after an action potential, transport activity needs to be regulated so that they do not pump out neurotransmitters after vesicle fusion. Using cryo–electron microscopy, Li et al. determined the structure of a vesicular glutamate transporter from rat that unveils some of the distinctive features that enable it to function properly in two distinct cellular environments. An allosteric pH sensor, proposed to be a glutamate residue, gates binding of the substrate glutamate and simultaneously permits binding and counterflow of chloride ions. This molecular traffic light allows for a single ion channel to behave appropriately in different contexts. Science , this issue p. 893

Funder

National Institutes of Health

National Institute of Mental Health

National Institute of Neurological Disorders and Stroke

American Heart Association

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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