Temperature-dependent iron motion in extremophile rubredoxins - no need for 'corresponding states'.

Corresponding States Extremophile Hyperthermophile Iron-Sulfur Psychrophile Rubredoxin

Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
28 May 2024
Historique:
received: 15 12 2023
accepted: 15 05 2024
medline: 29 5 2024
pubmed: 29 5 2024
entrez: 28 5 2024
Statut: epublish

Résumé

Extremophile organisms are known that can metabolize at temperatures down to - 25 °C (psychrophiles) and up to 122 °C (hyperthermophiles). Understanding viability under extreme conditions is relevant for human health, biotechnological applications, and our search for life elsewhere in the universe. Information about the stability and dynamics of proteins under environmental extremes is an important factor in this regard. Here we compare the dynamics of small Fe-S proteins - rubredoxins - from psychrophilic and hyperthermophilic microorganisms, using three different nuclear techniques as well as molecular dynamics calculations to quantify motion at the Fe site. The theory of 'corresponding states' posits that homologous proteins from different extremophiles have comparable flexibilities at the optimum growth temperatures of their respective organisms. Although 'corresponding states' would predict greater flexibility for rubredoxins that operate at low temperatures, we find that from 4 to 300 K, the dynamics of the Fe sites in these homologous proteins are essentially equivalent.

Identifiants

pubmed: 38806591
doi: 10.1038/s41598-024-62261-2
pii: 10.1038/s41598-024-62261-2
doi:

Substances chimiques

Iron E1UOL152H7
Rubredoxins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

12197

Subventions

Organisme : NIH HHS
ID : GM-65440
Pays : United States
Organisme : NIH HHS
ID : GM-125924
Pays : United States
Organisme : NSF
ID : MCB-2149122

Informations de copyright

© 2024. The Author(s).

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Auteurs

Francis E Jenney (FE)

Georgia Campus, Philadelphia College of Osteopathic Medicine, Suwanee, GA, 30024, USA.

Hongxin Wang (H)

SETI Institute, Mountain View, CA, 94043, USA.

Simon J George (SJ)

SETI Institute, Mountain View, CA, 94043, USA.

Jin Xiong (J)

Department of Chemistry, Carnegie Mellon University, Pittsburgh, PA, 15213, USA.

Yisong Guo (Y)

Department of Chemistry, Carnegie Mellon University, Pittsburgh, PA, 15213, USA.

Leland B Gee (LB)

LCLS, SLAC National Laboratory, Stanford, CA, 94025, USA.

Juan José Marizcurrena (JJ)

Universidad de La República, Montevideo, Uruguay.

Susana Castro-Sowinski (S)

Universidad de La República, Montevideo, Uruguay.

Anna Staskiewicz (A)

Georgia Campus, Philadelphia College of Osteopathic Medicine, Suwanee, GA, 30024, USA.

Yoshitaka Yoda (Y)

Precision Spectroscopy Division, SPring-8/JASRI, Sayo, Hyogo, 679-5198, Japan.

Michael Y Hu (MY)

Advanced Photon Source, Argonne National Laboratory, Lemont, IL, 60439, USA.

Kenji Tamasaku (K)

RIKEN/SPring-8 Center, Hyogo, 679-5148, Japan.

Nobumoto Nagasawa (N)

Precision Spectroscopy Division, SPring-8/JASRI, Sayo, Hyogo, 679-5198, Japan.

Lei Li (L)

Synchrotron Radiation Research Center, Hyogo, 679-5165, Japan.

Hiroaki Matsuura (H)

RIKEN/SPring-8 Center, Hyogo, 679-5148, Japan.

Tzanko Doukov (T)

SSRL, SLAC National Laboratory, Stanford, CA, 94025, USA.

Stephen P Cramer (SP)

SETI Institute, Mountain View, CA, 94043, USA. spjcramer@mac.com.

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