Expanding the scope of resonance Raman spectroscopy in hydrogenase research: New observable states and reporter vibrations.

IR spectroscopy [NiFe] hydrogenase active site cryogenic temperature iron‑sulfur cluster resonance Raman spectroscopy

Journal

Journal of inorganic biochemistry
ISSN: 1873-3344
Titre abrégé: J Inorg Biochem
Pays: United States
ID NLM: 7905788

Informations de publication

Date de publication:
19 Sep 2024
Historique:
received: 27 07 2024
revised: 12 09 2024
accepted: 17 09 2024
medline: 27 9 2024
pubmed: 27 9 2024
entrez: 26 9 2024
Statut: aheadofprint

Résumé

Oxygen-tolerant [NiFe] hydrogenases are valuable blueprints for the activation and evolution of molecular hydrogen under application-relevant conditions. Vibrational spectroscopic techniques play a key role in the investigation of these metalloenzymes. For instance, resonance Raman spectroscopy has been introduced as a site-selective approach for probing metal-ligand coordinates of the [NiFe] active site and FeS clusters. Despite its success, this approach is still challenged by a limited number of detectable active-site states - due to missing resonance enhancement or intrinsic light sensitivity - and difficulties in their assignment. Utilizing two oxygen-tolerant [NiFe] hydrogenases as model systems, we illustrate how these challenges can be met by extending excitation and detection wavelength regimes in resonance Raman spectroscopic studies. Specifically, we observe that this technique does not only probe low-frequency metal-ligand vibrations but also high-frequency intra-ligand modes of the diatomic CO/CN

Identifiants

pubmed: 39326301
pii: S0162-0134(24)00265-4
doi: 10.1016/j.jinorgbio.2024.112741
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

112741

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Cornelius C M Bernitzky (CCM)

Freie Universität Berlin, Fachbereich Physik, Arnimallee 14, D-14195 Berlin, Germany; Technische Universität Berlin, Institut für Chemie, PC 14, Straße des 17. Juni 135, 10623 Berlin, Germany.

Giorgio Caserta (G)

Technische Universität Berlin, Institut für Chemie, PC 14, Straße des 17. Juni 135, 10623 Berlin, Germany.

Stefan Frielingsdorf (S)

Technische Universität Berlin, Institut für Chemie, PC 14, Straße des 17. Juni 135, 10623 Berlin, Germany.

Janna Schoknecht (J)

Technische Universität Berlin, Institut für Chemie, PC 14, Straße des 17. Juni 135, 10623 Berlin, Germany.

Andrea Schmidt (A)

Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Institute for Medical Physics and Biophysics, Group Structural Biology of Cellular Signaling, Charitéplatz 1, D-10117 Berlin, Germany.

Patrick Scheerer (P)

Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Institute for Medical Physics and Biophysics, Group Structural Biology of Cellular Signaling, Charitéplatz 1, D-10117 Berlin, Germany.

Oliver Lenz (O)

Technische Universität Berlin, Institut für Chemie, PC 14, Straße des 17. Juni 135, 10623 Berlin, Germany.

Peter Hildebrandt (P)

Technische Universität Berlin, Institut für Chemie, PC 14, Straße des 17. Juni 135, 10623 Berlin, Germany.

Christian Lorent (C)

Technische Universität Berlin, Institut für Chemie, PC 14, Straße des 17. Juni 135, 10623 Berlin, Germany. Electronic address: christian.lorent@tu-berlin.de.

Ingo Zebger (I)

Technische Universität Berlin, Institut für Chemie, PC 14, Straße des 17. Juni 135, 10623 Berlin, Germany. Electronic address: ingo.zebger@tu-berlin.de.

Marius Horch (M)

Freie Universität Berlin, Fachbereich Physik, Arnimallee 14, D-14195 Berlin, Germany. Electronic address: marius.horch@fu-berlin.de.

Classifications MeSH