通过靶向蛋白降解识别和表征癌症脆弱性

Q1 Pharmacology, Toxicology and Pharmaceutics
Cristina Mayor-Ruiz, Georg E. Winter
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引用次数: 24

摘要

靶蛋白降解(Target(ed) protein degradation, TPD)是一种新的药物发现模式,也是一种很有前景的治疗策略。TPD是基于通过重定向泛素E3连接酶的泛素化活性来催化蛋白质降解的小分子。其独特的分子药理学使其在细胞和体内检测中具有强大的选择性和快速消除蛋白质的能力。除了可能的临床应用之外,TPD也正在成为传统药理学或遗传扰动策略的一种有吸引力的替代方案。直接作用的降解剂以及化学遗传学衍生物为临床前鉴定、表征和治疗靶点的机制验证提供了独特的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification and characterization of cancer vulnerabilities via targeted protein degradation

Target(ed) protein degradation (TPD) is a novel paradigm in drug discovery and a promising therapeutic strategy. TPD is based on small-molecules that catalyze the degradation of proteins by re-directing the ubiquitination activity of ubiquitin E3 ligases. Its unique molecular pharmacology enables robust, selective and fast elimination of proteins in cellular assays and in vivo. In addition to possible clinical applications, TPD is also emerging as an attractive alternative to traditional pharmacologic or genetic perturbation strategies. Directly acting degraders, as well as chemical-genetics derivatives offer unique opportunities in the pre-clinical identification, characterization and mechanistic validation of therapeutic targets.

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来源期刊
Drug Discovery Today: Technologies
Drug Discovery Today: Technologies Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
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期刊介绍: Discovery Today: Technologies compares different technological tools and techniques used from the discovery of new drug targets through to the launch of new medicines.
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