| Literature DB >> 33319748 |
Katelyn Sweeney1,2,3, Hanna Kim4, Xiaohui Yan4, Zachary M March5,6, Laura M Castellano5,7, Meredith E Jackrel5, JiaBei Lin5, Edward Chuang5,7, Edward Gomes5, Corey W Willicott4, Karolina Michalska8,9, Robert P Jedrzejczak8, Andrzej Joachimiak8,9, Kim A Caldwell4, Guy A Caldwell4, Ophir Shalem1,2,3, James Shorter5,6,2,7.
Abstract
The AAA+ protein disaggregase, Hsp104, increases fitness under stress by reversing stress-induced protein aggregation. Natural Hsp104 variants might exist with enhanced, selective activity against neurodegenerative disease substrates. However, natural Hsp104 variation remains largely unexplored. Here, we screened a cross-kingdom collection of Hsp104 homologs in yeast proteotoxicity models. Prokaryotic ClpG reduced TDP-43, FUS, and α-synuclein toxicity, whereas prokaryotic ClpB and hyperactive variants were ineffective. We uncovered therapeutic genetic variation among eukaryotic Hsp104 homologs that specifically antagonized TDP-43 condensation and toxicity in yeast and TDP-43 aggregation in human cells. We also uncovered distinct eukaryotic Hsp104 homologs that selectively antagonized α-synuclein condensation and toxicity in yeast and dopaminergic neurodegeneration in C. elegans. Surprisingly, this therapeutic variation did not manifest as enhanced disaggregase activity, but rather as increased passive inhibition of aggregation of specific substrates. By exploring natural tuning of this passive Hsp104 activity, we elucidated enhanced, substrate-specific agents that counter proteotoxicity underlying neurodegeneration.Entities:
Keywords: C. elegans; Hsp104; S. cerevisiae; TDP-43; alpha-synuclein; biochemistry; chaperone; chemical biology; disaggregase; genetics; genomics; protein misfolding
Mesh:
Substances:
Year: 2020 PMID: 33319748 PMCID: PMC7785292 DOI: 10.7554/eLife.57457
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140