Control of protein activity by photoinduced spin polarized charge reorganization.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
30 08 2022
Historique:
entrez: 22 8 2022
pubmed: 23 8 2022
medline: 25 8 2022
Statut: ppublish

Résumé

Considerable electric fields are present within living cells, and the role of bioelectricity has been well established at the organismal level. Yet much remains to be learned about electric-field effects on protein function. Here, we use phototriggered charge injection from a site-specifically attached ruthenium photosensitizer to directly demonstrate the effect of dynamic charge redistribution within a protein. We find that binding of an antibody to phosphoglycerate kinase (PGK) is increased twofold under illumination. Remarkably, illumination is found to suppress the enzymatic activity of PGK by a factor as large as three. These responses are sensitive to the photosensitizer position on the protein. Surprisingly, left (but not right) circularly polarized light elicits these responses, indicating that the electrons involved in the observed dynamics are spin polarized, due to spin filtration by protein chiral structures. Our results directly establish the contribution of electrical polarization as an allosteric signal within proteins. Future experiments with phototriggered charge injection will allow delineation of charge rearrangement pathways within proteins and will further depict their effects on protein function.

Identifiants

pubmed: 35994638
doi: 10.1073/pnas.2204735119
pmc: PMC9436351
doi:

Substances chimiques

Photosensitizing Agents 0
Proteins 0
Ruthenium 7UI0TKC3U5

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2204735119

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK019038
Pays : United States

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Auteurs

Shirsendu Ghosh (S)

Department of Chemical and Biological Physics, Weizmann Institute of Science, Rehovot, Israel.

Koyel Banerjee-Ghosh (K)

Department of Chemical and Biological Physics, Weizmann Institute of Science, Rehovot, Israel.
Department of Chemistry, Indian Institute of Technology Hyderabad, Kandi, Sangareddy-502285, Telangana, India.

Dorit Levy (D)

Department of Chemical and Biological Physics, Weizmann Institute of Science, Rehovot, Israel.

David Scheerer (D)

Department of Chemical and Biological Physics, Weizmann Institute of Science, Rehovot, Israel.

Inbal Riven (I)

Department of Chemical and Biological Physics, Weizmann Institute of Science, Rehovot, Israel.

Jieun Shin (J)

Beckman Institute, California Institute of Technology, Pasadena, CA 91125.

Harry B Gray (HB)

Beckman Institute, California Institute of Technology, Pasadena, CA 91125.

Ron Naaman (R)

Department of Chemical and Biological Physics, Weizmann Institute of Science, Rehovot, Israel.

Gilad Haran (G)

Department of Chemical and Biological Physics, Weizmann Institute of Science, Rehovot, Israel.

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Classifications MeSH