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Replacing a cysteine ligand by selenocysteine in a [NiFe]-hydrogenase unlocks hydrogen production activity and addresses the role of concerted proton-coupled electron transfer in electrocatalytic reversibility

Abstract:
Hydrogenases catalyze hydrogen/proton interconversion that is normally electrochemically reversible (having minimal overpotential requirement), a special property otherwise almost exclusive to platinum metals. The mechanism of [NiFe]-hydrogenases includes a long-range proton-coupled electron-transfer process involving a specific Ni-coordinated cysteine and the carboxylate of a nearby glutamate. A variant in which this cysteine has been exchanged for selenocysteine displays two distinct changes in electrocatalytic properties, as determined by protein film voltammetry. First, proton reduction, even in the presence of H2 (a strong product inhibitor), is greatly enhanced relative to H2 oxidation: this result parallels a characteristic of natural [NiFeSe]-hydrogenases which are superior H2 production catalysts. Second, an inflection (an S-shaped “twist” in the trace) appears around the formal potential, the small overpotentials introduced in each direction (oxidation and reduction) signaling a departure from electrocatalytic reversibility. Concerted proton–electron transfer offers a lower energy pathway compared to stepwise transfers. Given the much lower proton affinity of Se compared to that of S, the inflection provides compelling evidence that concerted proton–electron transfer is important in determining why [NiFe]-hydrogenases are reversible electrocatalysts.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1021/jacs.4c03489

Authors


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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Role:
Author
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Role:
Author
ORCID:
0000-0003-0696-433X
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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Inorganic Chemistry
Oxford college:
Jesus College
Role:
Author
ORCID:
0000-0001-6444-9382
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Role:
Author
ORCID:
0000-0002-3077-8986


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Funder identifier:
https://ror.org/0472cxd90
Grant:
819580
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Funder identifier:
https://ror.org/00cwqg982
Grant:
BB/L009722/1
BB/I022309/1


Publisher:
American Chemical Society
Journal:
Journal of the American Chemical Society More from this journal
Volume:
146
Issue:
25
Pages:
16971–16976
Place of publication:
United States
Publication date:
2024-05-15
Acceptance date:
2024-05-10
DOI:
EISSN:
1520-5126
ISSN:
0002-7863
Pmid:
38747098


Language:
English
Pubs id:
1997030
Local pid:
pubs:1997030
Deposit date:
2024-06-11

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