Neurology Department at Huashan Hospital, State Key Laboratory of Medical Neurobiology, and Ministry of Education Frontiers Center for Brain Science, School of Life Sciences, Fudan University, Shanghai, China.
Department of Optical Science and Engineering, Shanghai Engineering Research Center of Ultra-Precision Optical Manufacturing, Key Laboratory of Micro and Nano Photonic Structures, Ministry of Education, Fudan University, Shanghai, China.
Trends Pharmacol Sci. 2020 Jul;41(7):464-474. doi: 10.1016/j.tips.2020.04.005. Epub 2020 Apr 23.
Traditional drug discovery focuses on identifying direct inhibitors of target proteins. This typically relies on a measurable biochemical readout and accessible binding sites whose occupancy influences the function of the target protein. These requirements preclude many disease-causing proteins from being 'druggable' targets, and these proteins are categorized as 'undruggable'. The proteolysis-targeting chimera (PROTAC) technology provides powerful tools to degrade these undruggable targets and has become a promising approach for drug discovery. However, the PROTAC technology has some limitations, and emerging new degrader technologies may greatly broaden the spectrum of targets that could be selectively degraded by harnessing a second major degradation pathway in cells. We review key emerging technologies that exploit the lysosomal degradation pathway and discuss their potential applications and limitations.
传统的药物发现侧重于识别靶蛋白的直接抑制剂。这通常依赖于可测量的生化读数和可及的结合位点,其占据会影响靶蛋白的功能。这些要求排除了许多导致疾病的蛋白质成为“可成药”的靶标,这些蛋白质被归类为“不可成药”。蛋白水解靶向嵌合体(PROTAC)技术为降解这些不可成药的靶标提供了强大的工具,已成为药物发现的一种有前途的方法。然而,PROTAC 技术存在一些局限性,新兴的降解剂技术可能通过利用细胞中的第二条主要降解途径,极大地拓宽可选择性降解的靶标范围。我们综述了利用溶酶体降解途径的关键新兴技术,并讨论了它们的潜在应用和局限性。