The Proteome Folding Problem and Cellular Proteostasis

被引:24
作者
Powers, Evan T. [1 ]
Gierasch, Lila M. [2 ,3 ]
机构
[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
基金
美国国家卫生研究院;
关键词
protein folding; proteome folding; proteostasis; chaperone; energy landscape; PHARMACOLOGICAL CHAPERONE THERAPY; LIQUID PHASE-SEPARATION; ENZYMATIC REACTIVATION; SUBSTRATE-SPECIFICITY; ALPHA-SYNUCLEIN; QUALITY CONTROL; DRIVING FORCES; GROEL BINDS; IN-VIVO; PROTEINS;
D O I
10.1016/j.jmb.2021.167197
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页数:11
相关论文
共 127 条
[41]   Counteracting chemical chaperone effects on the single-molecule α-synuclein structural landscape [J].
Ferreon, Allan Chris M. ;
Moosa, Mahdi Muhammad ;
Gambin, Yann ;
Deniz, Ashok A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (44) :17826-17831
[42]   Cryo-EM structures of tau filaments from Alzheimer's disease [J].
Fitzpatrick, Anthony W. P. ;
Falcon, Benjamin ;
He, Shaoda ;
Murzin, Alexey G. ;
Murshudov, Garib ;
Garringer, Holly J. ;
Crowther, R. Anthony ;
Ghetti, Bernardino ;
Goedert, Michel ;
Scheres, Sjors H. W. .
NATURE, 2017, 547 (7662) :185-+
[43]   Folding of newly translated proteins in vivo: The role of molecular chaperones [J].
Frydman, J .
ANNUAL REVIEW OF BIOCHEMISTRY, 2001, 70 :603-647
[44]  
FUCHS S, 1967, J BIOL CHEM, V242, P398
[45]  
Germain DP, 2009, INT J CLIN PHARM TH, V47, pS111
[46]   Energy landscapes of functional proteins are inherently risky [J].
Gershenson, Anne ;
Gierasch, Lila M. ;
Pastore, Annalisa ;
Radford, Sheena E. .
NATURE CHEMICAL BIOLOGY, 2014, 10 (11) :884-891
[47]   Progressive disruption of cellular protein folding in models of polyglutamine diseases [J].
Gidalevitz, T ;
Ben-Zvi, A ;
Ho, KH ;
Brignull, HR ;
Morimoto, RI .
SCIENCE, 2006, 311 (5766) :1471-1474
[48]  
GOLDBERGER RF, 1963, J BIOL CHEM, V238, P628
[49]   Peptidyl-prolyl cis-trans isomerases, a superfamily of ubiquitous folding catalysts [J].
Göthel, SF ;
Marahiel, MA .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1999, 55 (03) :423-436
[50]   Small molecule strategies to harness the unfolded protein response: where do we go from here? [J].
Grandjean, Julia M. D. ;
Wiseman, R. Luke .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2020, 295 (46) :15692-15711