Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Molecular principles of redox-coupled sodium pumping of the ancient Rnf machinery
Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics.ORCID iD: 0000-0002-2964-5908
Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics.ORCID iD: 0000-0003-2575-9913
Show others and affiliations
Number of Authors: 102025 (English)In: Nature Communications, E-ISSN 2041-1723, Vol. 16, article id 2302Article in journal (Refereed) Published
Abstract [en]

The Rnf complex is the primary respiratory enzyme of several anaerobic prokaryotes that transfers electrons from ferredoxin to NAD+ and pumps ions (Na+ or H+) across a membrane, powering ATP synthesis. Rnf is widespread in primordial organisms and the evolutionary predecessor of the Na+-pumping NADH-quinone oxidoreductase (Nqr). By running in reverse, Rnf uses the electrochemical ion gradient to drive ferredoxin reduction with NADH, providing low potential electrons for nitrogenases and CO2 reductases. Yet, the molecular principles that couple the long-range electron transfer to Na+ translocation remain elusive. Here, we resolve key functional states along the electron transfer pathway in the Na+-pumping Rnf complex from Acetobacterium woodii using redox-controlled cryo-electron microscopy that, in combination with biochemical functional assays and atomistic molecular simulations, provide key insight into the redox-driven Na+ pumping mechanism. We show that the reduction of the unique membrane-embedded [2Fe2S] cluster electrostatically attracts Na+, and in turn, triggers an inward/outward transition with alternating membrane access driving the Na+ pump and the reduction of NAD+. Our study unveils an ancient mechanism for redox-driven ion pumping, and provides key understanding of the fundamental principles governing energy conversion in biological systems.

Place, publisher, year, edition, pages
2025. Vol. 16, article id 2302
Keywords [en]
Bioenergetics, Cryoelectron microscopy, Oxidoreductases, Sodium channels
National Category
Biochemistry
Identifiers
URN: urn:nbn:se:su:diva-241799DOI: 10.1038/s41467-025-57375-8ISI: 001439808600028PubMedID: 40055346Scopus ID: 2-s2.0-86000324494OAI: oai:DiVA.org:su-241799DiVA, id: diva2:1951583
Available from: 2025-04-11 Created: 2025-04-11 Last updated: 2025-08-04Bibliographically approved
In thesis
1. Exploring Energy Conversion Mechanisms in Respiratory Enzymes
Open this publication in new window or tab >>Exploring Energy Conversion Mechanisms in Respiratory Enzymes
2025 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

All life fundamentally relies on the efficient capture and conversion of energy into forms that support vital biochemical processes. Central to this process is the respiratory chain, a set of membrane-bound protein complexes that harness energy-rich molecules to drive ion translocation across biological membranes. This process generates an electrochemical gradient, known as the proton motive force (pmf) or sodium motive force (smf), that in turn powers the synthesis of ATP, the universal energy currency of the cell. In this thesis, the mechanistic principles underlying the function of respiratory enzymes are explored using a combination of classical molecular dynamics simulations, quantum mechanical methods, and hybrid quantum mechanics/molecular mechanics (QM/MM) calculations.

The respiratory Complex I couples the oxidation of NADH and the reduction of quinone to the translocation of four protons across biological membranes. Our results indicate that this coupling is mediated by a network of charged residues. Switching within this network triggers a conformational change of a key gating residue, thereby linking the redox reaction to ion translocation. Additionally, we identify proton translocation pathways through the membrane domain of Complex I, whose dynamics are governed by the conformation of conserved ion pairs. We investigate the mechanism of oxygen reduction and quinol oxidation by the alternative oxidase (AOX), and find that the diiron center forms a ferryl/ferric intermediate, which is reduced by the quinol in a highly exothermic reaction. To understand what drives supercomplex (SC) formation, we analyze their membrane interactions and observe that the association of Complex I and III2 into SCs reduces membrane strain. Finally, we examine the redox-coupled Na+ translocation mechanism of the Rnf complex and identify conformation dependent Na+ binding sites, based on which we propose a mechanism for ion transport. Together, the results presented in this thesis provide new insights into the mechanistic principles that govern membrane-bound respiratory enzymes.

Place, publisher, year, edition, pages
Stockholm: Department of Biochemistry and Biophysics, Stockholm University, 2025. p. 68
Keywords
Bioenergetics, Respiratory Enzymes, Proton Transfer, Energy Transduction, Multiscale Simulations
National Category
Biophysics Theoretical Chemistry Biochemistry
Research subject
Biochemistry
Identifiers
urn:nbn:se:su:diva-245310 (URN)978-91-8107-336-2 (ISBN)978-91-8107-337-9 (ISBN)
Public defence
2025-09-22, Hörsal 8, Hus D, Universitetsvägen 14 and online via Zoom, public link is available at the department website, Stockholm, 09:00 (English)
Opponent
Supervisors
Available from: 2025-08-28 Created: 2025-08-04 Last updated: 2025-08-20Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMedScopus

Authority records

Kim, HyunhoSaura, PatriciaKaila, Ville R. I.

Search in DiVA

By author/editor
Kim, HyunhoSaura, PatriciaKaila, Ville R. I.
By organisation
Department of Biochemistry and Biophysics
In the same journal
Nature Communications
Biochemistry

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 46 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf