Evidence map›Paper›PMID 41933102›Full record

ArticleJournal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry2026

[FeFe] hydrogenases with modified azadithiolate bridgeheads serve as unidirectional hydrogen oxidation catalysts.

Manon T Lachmann, James A Birrell, Simone Morra, Patricia Rodríguez-Maciá

Erratum issuedAbstract read
In one paragraph

Article in Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Manon T LachmannSchool of Chemistry and Leicester Institute for Structural and Chemical Biology, University of Leicester, University Road, Leicester, LE1 7RH, UK.ORCID http://orcid.org/0009-0001-1631-0113
James A BirrellSchool of Life Sciences, University of Essex, Wivenhoe Park, Colchester, CO4 3SQ, UK.ORCID http://orcid.org/0000-0002-0939-0573
Simone MorraFaculty of Engineering, University of Nottingham, Coates Building, University Park, Nottingham, NG7 2RD, UK.ORCID http://orcid.org/0000-0003-1341-191X
Patricia Rodríguez-MaciáSchool of Chemistry and Leicester Institute for Structural and Chemical Biology, University of Leicester, University Road, Leicester, LE1 7RH, UK. prm28@leicester.ac.uk.ORCID http://orcid.org/0000-0003-3513-0115

Funding

Royal Society RG\R2\232336Royal Society RGS\R1\231433Royal Society of Chemistry R22-2594924113Royal Society of Chemistry R23-6753486967University of Leicester Future 50 Scholarship
6 · The paper itself

Abstract

Semi-synthetic [FeFe] hydrogenases hold exciting potential as tuneable artificial metalloenzymes for efficient hydrogen conversion (H2 ⇌ 2 H+ + 2e−). This work investigates the role of the bridgehead ligand in the [FeFe] hydrogenase active site through the study of two bridgehead-modified active-site variants (2-oxapropane 1,3-dithiolate, ODT, and propane 1,3-dithiolate, PDT). Replacing the native 2-azapropane 1,3-dithiolate (ADT) bridgehead with ODT or PDT significantly modifies the active site’s electronic structure and disrupts proton-transfer; yet, some catalytic activity remains, suggesting that alternative catalytic pathways may exist. Notably, when adsorbed onto an electrode, the ODT enzymes operate as proficient catalysts for hydrogen oxidation at higher oxidative overpotentials, achieving current densities of up to 1 mA cm− 2, comparable to those observed for the respective ADT enzyme under the same conditions. Electrochemical analysis reveals similar catalytic behaviour between the ODT and PDT enzymes, suggesting that a proton transfer pathway between the active site and the protein environment still operates, albeit disrupted, in both bridgehead variants under these conditions. Insights into the electronic and catalytic interplay of these modifications could advance the optimisation of semi-synthetic [FeFe] hydrogenases and design of new bioinspired catalysts.

Indexed as

Aza CompoundsHydrogenHydrogenaseIron-Sulfur ProteinsSulfhydryl CompoundsCatalysisCatalytic DomainModels, MolecularOxidation-ReductionAza CompoundsHydrogenHydrogenaseiron hydrogenaseIron-Sulfur ProteinsSulfhydryl CompoundsActive-site variantElectrochemistry[FeFe] hydrogenaseHydrogen oxidationProton transfer pathwaySpectroscopy

Identifiers

PMID41933102
PMCPMC13287228

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.