| Literature DB >> 33597714 |
Sensen Zhang1, Jun Zhou1, Yuebin Zhang2, Tianya Liu1, Perrine Friedel3, Wei Zhuo1, Suma Somasekharan3, Kasturi Roy3, Laixing Zhang1, Yang Liu1, Xianbin Meng4, Haiteng Deng4, Wenwen Zeng5, Guohui Li6, Biff Forbush7, Maojun Yang8,9.
Abstract
NKCC and KCC transporters mediate coupled transport of Na++K++Cl- and K++Cl- across the plasma membrane, thus regulating cell Cl- concentration and cell volume and playing critical roles in transepithelial salt and water transport and in neuronal excitability. The function of these transporters has been intensively studied, but a mechanistic understanding has awaited structural studies of the transporters. Here, we present the cryo-electron microscopy (cryo-EM) structures of the two neuronal cation-chloride cotransporters human NKCC1 (SLC12A2) and mouse KCC2 (SLC12A5), along with computational analysis and functional characterization. These structures highlight essential residues in ion transport and allow us to propose mechanisms by which phosphorylation regulates transport activity.Entities:
Year: 2021 PMID: 33597714 PMCID: PMC7889885 DOI: 10.1038/s42003-021-01750-w
Source DB: PubMed Journal: Commun Biol ISSN: 2399-3642