药物发现
神经退行性变
泛素
生物
计算生物学
泛素连接酶
药物开发
蛋白酶体
医学
生物信息学
药品
药理学
疾病
遗传学
内科学
基因
作者
Jeanine A. Harrigan,Xavier Jacq,Niall M.B. Martin,Stephen P. Jackson
摘要
More than a decade after a Nobel Prize was awarded for the discovery of the ubiquitin-proteasome system and clinical approval of proteasome and ubiquitin E3 ligase inhibitors, first-generation deubiquitylating enzyme (DUB) inhibitors are now approaching clinical trials. However, although our knowledge of the physiological and pathophysiological roles of DUBs has evolved tremendously, the clinical development of selective DUB inhibitors has been challenging. In this Review, we discuss these issues and highlight recent advances in our understanding of DUB enzymology and biology as well as technological improvements that have contributed to the current interest in DUBs as therapeutic targets in diseases ranging from oncology to neurodegeneration.
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