Repurposing Hsp104 to Antagonize Seminal Amyloid and Counter HIV Infection-Reference-Cited by-同舟云学术

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Repurposing Hsp104 to Antagonize Seminal Amyloid and Counter HIV Infection

Published:2015-08 Issue:8 Volume:22 Page:1074-1086
ISSN:1074-5521
Container-title:Chemistry & Biology
language:en
Short-container-title:Chemistry & Biology

Author:

Castellano Laura M.,Bart Stephen M.,Holmes Veronica M.,Weissman Drew,Shorter James

Funder

NSF Graduate Research Fellowship

Bill and Melinda Gates Foundation Grand Challenges Explorations Award

Linda Pechenik Montague Investigator Award

NIH

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,General Medicine,Biochemistry

Reference53 articles.

1. Dynamic droplets: the role of cytoplasmic inclusions in stress, function, and disease;Amen;Cell. Mol. Life Sci.,2015

2. Naturally occurring fragments from two distinct regions of the prostatic acid phosphatase form amyloidogenic enhancers of HIV infection;Arnold;J. Virol.,2012

3. The amino-terminal domain of ClpB supports binding to strongly aggregated proteins;Barnett;J. Biol. Chem.,2005

4. Substrate binding to the molecular chaperone Hsp104 and its regulation by nucleotides;Bosl;J. Biol. Chem.,2005

5. The amyloidogenic SEVI precursor, PAP248-286, is highly unfolded in solution despite an underlying helical tendency;Brender;Biochim. Biophys. Acta,2011

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3. The Extracellular Molecular Chaperone Clusterin Inhibits Amyloid Fibril Formation and Suppresses Cytotoxicity Associated with Semen-Derived Enhancer of Virus Infection (SEVI);Cells;2022-10-17

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