可药性
工作流程
计算机科学
合成生物学
数据科学
药物发现
计算生物学
自动化
表型筛选
纳米技术
生化工程
信息学
新兴技术
工程类
转化研究
高含量筛选
风险分析(工程)
作者
Baoli Ding,Xiaotong Chen,Yulu Chen,Ji Cao,Bo Yang,Li Jiang,Cheng‐Liang Zhu
标识
DOI:10.1002/chem.202503641
摘要
Targeted protein degradation (TPD) is significantly expanding the druggable landscape to include proteins that are intractable to conventional occupancy-based inhibition. However, the discovery of targeted protein degraders is often less efficient due to their structural complexity and the labor-intensive nature of traditional medicinal chemistry campaigns. To capture the recent advances developed to streamline and accelerate degrader discovery, this review summarizes enabling synthetic methodologies and state-of-the-art screening strategies specialized for this field. From the well-established click chemistry to emerging late-stage functionalization, we highlight a wide array of robust and versatile chemistries that facilitate the rapid construction of diverse degrader libraries. Moreover, we elucidate how these synthetic toolkits synergize with screening tactics to expand the biological space and maximize the efficiency of identifying promising degrader candidates. Furthermore, we underscore that evolving automation and robotic workflows are integrating with these synthetic and screening strategies to propel a new era of degrader discovery. By providing a comprehensive overview and critical perspectives on these advancements, this review aims to offer a practical roadmap for researchers to streamline degrader synthesis and strategically screen their libraries, with the hope of inspiring continued innovation to expedite the discovery of novel degraders with both biological and therapeutic importance.
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