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Molecular Cell|April 14, 2009
Motor mechanism for protein threading through Hsp104Petra Wendler, James Shorter, David Snead, et al.
Plos Biology|May 5, 2011
Molecular determinants and genetic modifiers of aggregation and toxicity for the ALS disease protein FUS/TLSZhihui Sun, Zamia Diaz, Xiaodong Fang, et al.
Molecular Cell|June 3, 2014
A cellular system that degrades misfolded proteins and protects against neurodegenerationLili Guo, Benoit I Giasson, Alex Glavis-Bloom, et al.
Nature|August 19, 2021
DAXX represents a new type of protein-folding enablerLiangqian Huang, Trisha Agrawal, Guixin Zhu, et al.
Biorxiv : the Preprint Server for Biology|November 26, 2025
Nuclear-import receptors remodel the dilute phase to suppress phase transitions of RNA-binding proteins with prion-like domainsMiriam Linsenmeier, Min Kyung Shinn, Thomas R Mumford, et al.
The Journal of Cell Biology|June 19, 2002
Sequential SNARE disassembly and GATE-16-GOS-28 complex assembly mediated by distinct NSF activities drives Golgi membrane fusionJoyce M M Muller, James Shorter, Richard Newman, et al.
Molecular Cell|August 14, 2018
Poly(ADP-Ribose) Prevents Pathological Phase Separation of TDP-43 by Promoting Liquid Demixing and Stress Granule LocalizationLeeanne McGurk, Edward Gomes, Lin Guo, et al.
Nature Structural & Molecular Biology|August 2, 2016
Spiral architecture of the Hsp104 disaggregase reveals the basis for polypeptide translocationAdam L Yokom, Stephanie N Gates, Meredith E Jackrel, et al.
Cell Reports|September 28, 2022
Unique structural features govern the activity of a human mitochondrial AAA+ disaggregase, Skd3Ryan R Cupo, Alexandrea N Rizo, Gabriel A Braun, et al.
The Journal of Biological Chemistry|November 28, 2013
Conserved distal loop residues in the Hsp104 and ClpB middle domain contact nucleotide-binding domain 2 and enable Hsp70-dependent protein disaggregationMorgan E Desantis, Elizabeth A Sweeny, David Snead, et al.
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