Open AccessProteostasis is adaptive: Balancing chaperone holdases against foldases
Author(s) -
Adam Mr de Graff,
David E. Mosedale,
Helen BeacockSharp,
Ken A. Dill,
David J. Grainger
Publication year - 2020
Publication title -
plos computational biology/plos computational biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.628
H-Index - 182
eISSN - 1553-7358
pISSN - 1553-734X
DOI - 10.1371/journal.pcbi.1008460
Subject(s) - proteostasis , proteome , foldase , protein folding , robustness (evolution) , chaperone (clinical) , biology , evolvability , microbiology and biotechnology , adaptation (eye) , computer science , bioinformatics , groel , biochemistry , neuroscience , genetics , medicine , escherichia coli , pathology , gene
Because a cell must adapt to different stresses and growth rates, its proteostasis system must too. How do cells detect and adjust proteome folding to different conditions? Here, we explore a biophysical cost-benefit principle, namely that the cell should keep its proteome as folded as possible at the minimum possible energy cost. This can be achieved by differential expression of chaperones–balancing foldases (which accelerate folding) against holdases (which act as parking spots). The model captures changes in the foldase-holdase ratio observed both within organisms during aging and across organisms of varying metabolic rates. This work describes a simple biophysical mechanism by which cellular proteostasis adapts to meet the needs of a changing growth environment.