Quantitative insights into the mechanism of proton conduction and selectivity for the human voltage-gated proton channel Hv1.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
17 Sep 2024
Historique:
medline: 11 9 2024
pubmed: 11 9 2024
entrez: 11 9 2024
Statut: ppublish

Résumé

Human voltage-gated proton (hHv1) channels are crucial for regulating essential biological processes such as immune cell respiratory burst, sperm capacitation, and cancer cell migration. Despite the significant concentration difference between protons and other ions in physiological conditions, hHv1 demonstrates remarkable proton selectivity. Our calculations of single-proton, cation, and anion permeation free energy profiles quantitatively demonstrate that the proton selectivity of the wild-type channel originates from its strong proton affinity via the titration of the key residues D112 and D174, although the channel imposes similar kinetic blocking effects for protons compared to other ions. A two-proton knock-on model is proposed to mathematically explain the electrophysiological measurements of the pH-dependent proton conductance in the conductive state. Moreover, it is shown that the anion selectivity of the D112N mutant channel is tied to impaired proton transport and substantial anion leakage.

Identifiants

pubmed: 39259593
doi: 10.1073/pnas.2407479121
doi:

Substances chimiques

HVCN1 protein, human 0
Protons 0
Ion Channels 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2407479121

Subventions

Organisme : HHS | NIH | National Institute of General Medical Sciences (NIGMS)
ID : R01GM053148
Organisme : HHS | NIH | National Institute of General Medical Sciences (NIGMS)
ID : R01GM098973
Organisme : NSF (NSF)
ID : OCI-1053575

Déclaration de conflit d'intérêts

Competing interests statement:The authors declare no competing interest.

Auteurs

Yu Liu (Y)

Department of Chemistry, Chicago Center for Theoretical Chemistry, Institute for Biophysical Dynamics, and James Frank Institute, University of Chicago, Chicago, IL 60637.

Chenghan Li (C)

Department of Chemistry, Chicago Center for Theoretical Chemistry, Institute for Biophysical Dynamics, and James Frank Institute, University of Chicago, Chicago, IL 60637.

J Alfredo Freites (JA)

Department of Chemistry, University of California, Irvine, CA 92697.

Douglas J Tobias (DJ)

Department of Chemistry, University of California, Irvine, CA 92697.

Gregory A Voth (GA)

Department of Chemistry, Chicago Center for Theoretical Chemistry, Institute for Biophysical Dynamics, and James Frank Institute, University of Chicago, Chicago, IL 60637.

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Classifications MeSH