Crystallographic Investigation and Selective Inhibition of Mutant Isocitrate Dehydrogenase.

Crystallographic Investigation and Selective Inhibition of Mutant Isocitrate Dehydrogenase.
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DOI:
10.1021/ml400036z
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发表时间:
2013-06-13
影响因子:
4.2
通讯作者:
Song, Yongcheng
Song, Yongcheng
中科院分区:
医学3区
文献类型:
--
作者:
Zheng, Baisong;Yao, Yuan;Liu, Zhen;Deng, Lisheng;Anglin, Justin L.;Jiang, Hong;Prasad, B. V. Venkataram;Song, Yongcheng

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Mutations in isocitrate dehydrogenase (IDH), a key enzyme in the tricarboxylic acid cycle, have recently been found in ~75% glioma and ~20% acute myeloid leukemia. Different from the wild-type enzyme, mutant IDH1 catalyzes the reduction of α-ketoglutaric acid to D-2-hydroxyglutaric acid. Strong evidence has shown mutant IDH1 represents a novel target for this type of cancer. We found two 1-hydroxypyridin-2-one compounds that are potent inhibitors of R132H and R132C IDH1 mutants with Ki values as low as 120 nM. These compounds exhibit >60-fold selectivity against wild-type IDH1 and can inhibit the production of D-2-hydroxyglutaric acid in IDH1 mutated cells, representing novel chemical probes for cancer biology studies. We also report the first inhibitor-bound crystal structures of IDH1(R132H), showing these inhibitors have H-bond, electrostatic and hydrophobic interactions with the mutant enzyme. Comparison with the substrate-bound IDH1 structures revealed the structural basis for the high enzyme selectivity of these compounds.
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