Literature DB >> 33639418

Interspecies Differences in Proteome Turnover Kinetics Are Correlated With Life Spans and Energetic Demands.

Kyle Swovick1, Denis Firsanov1, Kevin A Welle2, Jennifer R Hryhorenko2, John P Wise3, Craig George4, Todd L Sformo5, Andrei Seluanov1, Vera Gorbunova1, Sina Ghaemmaghami6.   

Abstract

Cells continually degrade and replace damaged proteins. However, the high energetic demand of protein turnover generates reactive oxygen species that compromise the long-term health of the proteome. Thus, the relationship between aging, protein turnover, and energetic demand remains unclear. Here, we used a proteomic approach to measure rates of protein turnover within primary fibroblasts isolated from a number of species with diverse life spans including the longest-lived mammal, the bowhead whale. We show that organismal life span is negatively correlated with turnover rates of highly abundant proteins. In comparison with mice, cells from long-lived naked mole rats have slower rates of protein turnover, lower levels of ATP production, and reduced reactive oxygen species levels. Despite having slower rates of protein turnover, naked mole rat cells tolerate protein misfolding stress more effectively than mouse cells. We suggest that in lieu of a rapid constitutive turnover, long-lived species may have evolved more energetically efficient mechanisms for selective detection and clearance of damaged proteins.
Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Protein turnove; aging; protein degradation; proteostasis; quantitative proteomics

Mesh:

Substances:

Year:  2021        PMID: 33639418      PMCID: PMC7950207          DOI: 10.1074/mcp.RA120.002301

Source DB:  PubMed          Journal:  Mol Cell Proteomics        ISSN: 1535-9476            Impact factor:   5.911


  8 in total

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Review 4.  In vivo assay and modelling of protein and mitochondrial turnover during aging.

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7.  Proteotype coevolution and quantitative diversity across 11 mammalian species.

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Review 8.  Cross-species comparisons and in vitro models to study tempo in development and homeostasis.

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  8 in total

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