Gambogic Acid, a Natural Product Inhibitor of Hsp90

被引:117
作者
Davenport, Jason [1 ]
Manjarrez, Jacob R. [1 ]
Peterson, Laura [2 ]
Krumm, Brian [1 ]
Blagg, Brian S. J. [2 ]
Matts, Robert L. [1 ]
机构
[1] Oklahoma State Univ, Dept Biochem & Mol Biol, Noble Res Ctr 246, Stillwater, OK 74078 USA
[2] Univ Kansas, Dept Med Chem, Lawrence, KS 66045 USA
来源
JOURNAL OF NATURAL PRODUCTS | 2011年 / 74卷 / 05期
关键词
PANCREATIC-CANCER CELLS; HIGH-AFFINITY BINDING; TYROSINE PHOSPHORYLATION; FIREFLY LUCIFERASE; INDUCED APOPTOSIS; TERMINAL DOMAIN; IN-VITRO; PROTEIN; KINASE; EXPRESSION;
D O I
10.1021/np200029q
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
A high-throughput screening of natural product libraries identified (-)-gambogic acid (1), a component of the exudate of Garcinia harburyi, as a potential Hsp90 inhibitor, in addition to the known Hsp90 inhibitor celastrol (2). Subsequent testing established that 1 inhibited cell proliferation, brought about the degradation of Hsp90 client proteins in cultured cells, and induced the expression of Hsp70 and Hsp90, which are hallmarks of Hsp90 inhibition. Gambogic acid also disrupted the interaction of Hsp90, Hsp70, and Cdc37 with the heme-regulated elF2 alpha. kinase (HRI, an Hsp90-dependent client) and blocked the maturation of HRI in vitro. Surface plasmon resonance spectroscopy indicated that 1 bound to the N-terminal domain of Hsp90 with a low micromolar K(d), in a manner that was not competitive with the Hsp90 inhibitor geldanamycin (3). Molecular docking experiments supported the posit that 1 binds Hsp90 at a site distinct from Hsp90s ATP binding pocket. The data obtained have firmly established 1 as a novel Hsp90 inhibitor and have provided evidence of a new site that can be targeted for the development of improved Hsp90 inhibitors.
引用
收藏
页码:1085 / 1092
页数:8
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