4.5 Article

Mechanistic Studies of Sansalvamide A-Amide: An Allosteric Modulator of Hsp90

Journal

ACS MEDICINAL CHEMISTRY LETTERS
Volume 1, Issue 1, Pages 4-8

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ml900003t

Keywords

Sansalvamide A-amide; Hsp90; cancer therapeutics

Funding

  1. San Diego State University
  2. Frasch Foundation [658-HF07]
  3. NIH [1U54CA132379-01A1, 1R01CA137873]
  4. NIH/NIGMS SDSU MARC [5T34GM08303]
  5. NIH MIRT
  6. NIW [T90DK07015]
  7. Howell Foundation
  8. HHMI
  9. FOGARTY INTERNATIONAL CENTER [T37TW000067] Funding Source: NIH RePORTER
  10. NATIONAL CANCER INSTITUTE [R01CA137873] Funding Source: NIH RePORTER

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Herein, we show that sansalvarnide A-amide (San A-amide), a structurally unique molecule, influences a subset of cancer-related pathways involving heat shock protein 90 (Hsp90) We show that San A-amide specifically binds to the N-middle domain of Hsp90 and allosterically disrupts the binding of proteins thought to interact with the Hsp90 C-terminal domain, while having no effect on an N-terminal domain client protein This unique mechanism suggests that San A-amide is a potential tool for studying C-terminal binding proteins of Hsp90 as well as a promising lead in the development of new cancer therapeutics

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