The Proteome Folding Problem and Cellular Proteostasis

JOURNAL OF MOLECULAR BIOLOGY

卷:433

Review

Powers, Evan T.¹  Gierasch, Lila M.^2,3 

[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA

[2] Univ Massachusetts, Dept Biochem & Mol Biol, Amherst, MA 01003 USA

[3] Univ Massachusetts, Dept Chem, Amherst, MA 01003 USA

关键词: protein folding;    proteome folding;    proteostasis;    chaperone;    energy landscape;   

DOI  :  10.1016/j.jmb.2021.167197

来源: Elsevier

【 摘 要 】

Stunning advances have been achieved in addressing the protein folding problem, providing deeper understanding of the mechanisms by which proteins navigate energy landscapes to reach their native states and enabling powerful algorithms to connect sequence to structure. However, the realities of the in vivo protein folding problem remain a challenge to reckon with. Here, we discuss the concept of the proteome folding problem-the problem of how organisms build and maintain a functional proteome-by admitting that folding energy landscapes are characterized by many misfolded states and that cells must deploy a network of chaperones and degradation enzymes to minimize deleterious impacts of these off-pathway species. The resulting proteostasis network is an inextricable part of in vivo protein folding and must be understood in detail if we are to solve the proteome folding problem. We discuss how the development of computational models for the proteostasis network's actions and the relationship to the biophysical properties of the proteome has begun to offer new insights and capabilities. (C) 2021 Elsevier Ltd. All rights reserved.

【 授权许可】

Free