Determination of <i>in cellulo</i> proteome molecular dynamics in different halophilic Archaea

While biophysical studies have unravelled properties of specific proteins <i>in vitro</i>, characterizing globally their native state within the cell remains a challenge. In particular, protein adaptation to harsh intracellular physical and chemical conditions is poorly understood. Extremophiles, which thrive in severe environments, are good models for the study of such adaptation. Five haloarchaeal species, isolated from hypersaline environments, were used to assess correlations between intracellular salt concentrations and molecular dynamics properties. <i>In cellulo</i> protein stability was measured using nano differential scanning fluorimetry, and neutron spectrometry was used to determine molecular dynamics resilience and global flexibility. It was found that high intracellular accumulation of Mg<sup>2+</sup> and low intracellular accumulation of K<sup>+</sup> were correlated with higher stability and resilience. Sequence traits associated with mean proteome halophilicity, such as decreased hydrophobicity and increased acidity, weighted by the relative abundance of each protein, were also correlated with stability and resilience. <i>Haloferax mediterranei</i>, however, was found to be an exception as its proteome showed the highest <i>in cellulo</i> molecular stability and resilience associated with fewest sequence traits related to halophilicity, highlighting the significance of the intracellular salt environment in determining proteome biophysical properties.

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Publication Details

Journal
Journal of The Royal Society Interface
Published
2025-03-01
DOI
https://doi.org/10.1098/rsif.2024.0630
Citations
1
Primary Topic
Mass Spectrometry Techniques and Applications
Type
article
Field-Weighted Citation Impact
0.76

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article

Determination of in cellulo proteome molecular dynamics in different halophilic Archaea

Lorenzo Carré, Bruno Franzetti, Giuseppe Zaccaı̈, Francesca Natali et al.
1 citations
Journal of The Royal Society Interface
Mass Spectrometry Techniques and Applications
0.76
article

Determination of in cellulo proteome molecular dynamics in different halophilic Archaea

Lorenzo Carré, Bruno Franzetti, Giuseppe Zaccaı̈, Francesca Natali, Vaitson Çumaku
article en
1 citations

Abstract

While biophysical studies have unravelled properties of specific proteins <i>in vitro</i>, characterizing globally their native state within the cell remains a challenge. In particular, protein adaptation to harsh intracellular physical and chemical conditions is poorly understood. Extremophiles, which thrive in severe environments, are good models for the study of such adaptation. Five haloarchaeal species, isolated from hypersaline environments, were used to assess correlations between intracellular salt concentrations and molecular dynamics properties. <i>In cellulo</i> protein stability was measured using nano differential scanning fluorimetry, and neutron spectrometry was used to determine molecular dynamics resilience and global flexibility. It was found that high intracellular accumulation of Mg<sup>2+</sup> and low intracellular accumulation of K<sup>+</sup> were correlated with higher stability and resilience. Sequence traits associated with mean proteome halophilicity, such as decreased hydrophobicity and increased acidity, weighted by the relative abundance of each protein, were also correlated with stability and resilience. <i>Haloferax mediterranei</i>, however, was found to be an exception as its proteome showed the highest <i>in cellulo</i> molecular stability and resilience associated with fewest sequence traits related to halophilicity, highlighting the significance of the intracellular salt environment in determining proteome biophysical properties.

Journal of The Royal Society InterfaceVol. 22(224)
Centre National de la Recherche Scientifique (FR), Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR), CEA Grenoble (FR), Istituto Officina dei Materiali (IT), Institut Laue-Langevin (FR), Institut de Biologie Structurale (FR), Université Grenoble Alpes (FR)
Agence Nationale de la Recherche, Centre National de la Recherche Scientifique, French Infrastructure for Integrated Structural Biology
Openalex Percentile: Top 34%
Mass Spectrometry Techniques and Applications
0.76
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