Phospho‐regulation, nucleotide binding and ion access control in potassium‐chloride cotransporters. (25th May 2021)

• Record Type: Journal Article
• Authors: Chi, Gamma; Ebenhoch, Rebecca; Man, Henry; Tang, Haiping; Tremblay, Laurence E; Reggiano, Gabriella; Qiu, Xingyu; Bohstedt, Tina; Liko, Idlir; Almeida, Fernando G; Garneau, Alexandre P; Wang, Dong; McKinley, Gavin; Moreau, Christophe P; Bountra, Kiran D; Abrusci, Patrizia; Mukhopadhyay, Shubhashish M M; Fernandez‐Cid, Alejandra; Slimani, Samira; Lavoie, Julie L; Burgess‐Brown, Nicola A; Tehan, Ben; DiMaio, Frank; Jazayeri, Ali; Isenring, Paul; Robinson, Carol V; Dürr, Katharina L
• Is Part Of: EMBO journal. Volume 40:Number 14(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-05-25
• Subjects: HDX‐MS -- nucleotide binding -- phospho‐regulation -- potassium‐chloride co‐transport -- solute carrier; Molecular biology -- Periodicals; 572.805
• DOI: 10.15252/embj.2020107294
• Languages: English
• ISSNs: 0261-4189

Abstract

Abstract: Potassium‐coupled chloride transporters (KCCs) play crucial roles in regulating cell volume and intracellular chloride concentration. They are characteristically inhibited under isotonic conditions via phospho‐regulatory sites located within the cytoplasmic termini. Decreased inhibitory phosphorylation in response to hypotonic cell swelling stimulates transport activity, and dysfunction of this regulatory process has been associated with various human diseases. Here, we present cryo‐EM structures of human KCC3b and KCC1, revealing structural determinants for phospho‐regulation in both N‐ and C‐termini. We show that phospho‐mimetic KCC3b is arrested in an inward‐facing state in which intracellular ion access is blocked by extensive contacts with the N‐terminus. In another mutant with increased isotonic transport activity, KCC1Δ19, this interdomain interaction is absent, likely due to a unique phospho‐regulatory site in the KCC1 N‐terminus. Furthermore, we map additional phosphorylation sites as well as a previously unknown ATP/ADP‐binding pocket in the large C‐terminal domain and show enhanced thermal stabilization of other CCCs by adenine nucleotides. These findings provide fundamentally new insights into the complex regulation of KCCs and may unlock innovative strategies for drug development. SYNOPSIS: Chloride extrusion by transmembrane transporters is critical for regulation of cell volume and intracellular ion concentration. Here, cryo‐EM combined with functional assays identifies structural determinants of human potassium‐coupled chloride transporter (KCCs) activation. Human KCC1 and KCC3b transporter structures solved in two different phospho‐regulatory states show substantial conformational rearrangements. A phospho‐mimetic KCC3b mutant is auto‐inhibited by a cytoplasmic N‐terminal segment, and arrested in an inward‐facing state. Protein dynamics assays reveal mobility differences between phospho‐inhibited and activated states. KCC1 C‐terminal domain contains a nucleotide binding motif engaging ATP and ADP. Abstract : Cryo‐EM structures uncover phosphorylation‐dependent protein dynamics and ATP/ADP binding of human KCC membrane transporters.