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Charge Transfer and Chemo-Mechanical Coupling in Respiratory Complex I

57 Pages Posted: 15 Apr 2020 Publication Status: Review Complete

See all articles by Chitrak Gupta

Chitrak Gupta

Arizona State University (ASU) - School of Molecular Sciences

Umesh Khaniya

City College of New York

Chun Kit Chan

University of Illinois at Urbana-Champaign

François Dehez

University of Lorraine

Mrinal Shekhar

University of Illinois at Urbana-Champaign - Center for Biophysics and Computational Biology; University of Illinois at Urbana-Champaign - Beckman Institute for Advanced Science and Technology

M. R. Gunner

City College of New York

Leonid Sazanov

Institute of Science and Technology Austria (ISTA)

Christophe Chipot

University of Lorraine

A. Singharoy

Arizona State University (ASU) - School of Molecular Sciences

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Abstract

The mitochondrial respiratory chain formed by five protein complexes utilizes energy from catabolic processes to synthesize ATP. Complex I, the first and the largest protein complex of the chain, harvests electrons from NADH to reduce quinone, while pumping protons across the mitochondrial membrane. Detailed knowledge of the working principle of such coupled charge-transfer processes remains fragmentary due to bottlenecks arising from large conformational transitions and their interplay with the hydrated proton pathways. A recent study has reported the crystallographic structure of complex I from Thermus thermophilus, encasing 16 subunits with 9 iron-sulfur clusters, which are reduced by electrons from NADH. Here, we have used large-scale molecular dynamics simulations to study the chemo-mechanical coupling between redox changes of the iron-sulfur clusters and conformational transitions across complex I. First, we identify the redox switches within complex I, which couple the dynamics of the quinone binding pocket to the site of NADH reduction. Second, our free-energy calculations reveal that the affinity of the quinone, specifically menaquinone, for the binding-site is higher than that of its reduced, menaquinol form – a design essential for menaquinol release. Third, long-range hydrogen-bond networks connecting the quinone-binding site to the TM subunits are found to be responsible for proton pumping. Random insertion of molecular oxygen in reduced complex I illuminates an enhanced access to the iron-sulfur clusters, conducive to the formation of reactive oxygen species. Our simulations reveal molecular design principles linking redox reactions and proton translocation in complex I.

Keywords: Respiratory chain, Complex I, Chemo-mechanical coupling, Charge transfer, Molecular simulations, Reactive oxygen species

Suggested Citation

Gupta, Chitrak and Khaniya, Umesh and Chan, Chun Kit and Dehez, François and Shekhar, Mrinal and Gunner, M. R. and Sazanov, Leonid and Chipot, Christophe and Singharoy, A., Charge Transfer and Chemo-Mechanical Coupling in Respiratory Complex I. Available at SSRN: https://ssrn.com/abstract=3566031 or http://dx.doi.org/10.2139/ssrn.3566031
This version of the paper has not been formally peer reviewed.

Chitrak Gupta

Arizona State University (ASU) - School of Molecular Sciences ( email )

Tempe, AZ
United States

Umesh Khaniya

City College of New York ( email )

Convert Avenue at 138th Street
New York, NY 10031
United States

Chun Kit Chan

University of Illinois at Urbana-Champaign ( email )

601 E John St
Champaign, IL Champaign 61820
United States

François Dehez

University of Lorraine ( email )

Lorraine
France

Mrinal Shekhar

University of Illinois at Urbana-Champaign - Center for Biophysics and Computational Biology

601 E John St
Champaign, IL 61820
United States

University of Illinois at Urbana-Champaign - Beckman Institute for Advanced Science and Technology

601 E John St
Champaign, IL 61820
United States

M. R. Gunner

City College of New York ( email )

Convert Avenue at 138th Street
New York, NY 10031
United States

Leonid Sazanov

Institute of Science and Technology Austria (ISTA) ( email )

Klosterneuburg, 3400
Austria

Christophe Chipot

University of Lorraine ( email )

Lorraine
France

A. Singharoy (Contact Author)

Arizona State University (ASU) - School of Molecular Sciences ( email )

Tempe, AZ 85287
United States

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