John R. Glover

Affiliations: 
University of Toronto, Toronto, ON, Canada 
Website:
http://biochemistry.utoronto.ca/glover/lab/
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"John Glover"
Mean distance: 7.34
 
SNBCP
Cross-listing: FlyTree - Cell Biology Tree

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Publications

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Rosenzweig R, Moradi S, Zarrine-Afsar A, et al. (2013) Unraveling the mechanism of protein disaggregation through a ClpB-DnaK interaction. Science (New York, N.Y.). 339: 1080-3
Helsen CW, Glover JR. (2012) A new perspective on Hsp104-mediated propagation and curing of the yeast prion [PSI (+) ]. Prion. 6: 234-9
Helsen CW, Glover JR. (2012) Insight into molecular basis of curing of [PSI+] prion by overexpression of 104-kDa heat shock protein (Hsp104). The Journal of Biological Chemistry. 287: 542-56
Glover JR, Lum R. (2009) Remodeling of protein aggregates by Hsp104. Protein and Peptide Letters. 16: 587-97
Lum R, Niggemann M, Glover JR. (2008) Peptide and protein binding in the axial channel of Hsp104. Insights into the mechanism of protein unfolding. The Journal of Biological Chemistry. 283: 30139-50
Mackay RG, Helsen CW, Tkach JM, et al. (2008) The C-terminal extension of Saccharomyces cerevisiae Hsp104 plays a role in oligomer assembly. Biochemistry. 47: 1918-27
Tkach JM, Glover JR. (2008) Nucleocytoplasmic trafficking of the molecular chaperone Hsp104 in unstressed and heat-shocked cells. Traffic (Copenhagen, Denmark). 9: 39-56
Tkach JM, Glover JR. (2006) Hsp104p: A protein disaggregase Topics in Current Genetics. 16: 65-90
Mosser DD, Ho S, Glover JR. (2004) Saccharomyces cerevisiae Hsp104 enhances the chaperone capacity of human cells and inhibits heat stress-induced proapoptotic signaling. Biochemistry. 43: 8107-15
Tkach JM, Glover JR. (2004) Amino acid substitutions in the C-terminal AAA+ module of Hsp104 prevent substrate recognition by disrupting oligomerization and cause high temperature inactivation. The Journal of Biological Chemistry. 279: 35692-701
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