结合
连接器
化学
体内
毒素
肽
连接蛋白
药理学
生物化学
生物
细胞粘附
生物技术
数学分析
细胞
操作系统
计算机科学
数学
作者
Gemma Mudd,Heather S. Scott,Liuhong Chen,Katerine Van Rietschoten,Gabriela Ivanova-Berndt,Katarzyna Dzionek,Amy Brown,Sophie Watcham,Lewi White,Peter U. Park,Phil Jeffrey,Mike Rigby,Paul Beswick
标识
DOI:10.1021/acs.jmedchem.2c00065
摘要
Bicycle toxin conjugates (BTCs) are a promising new class of molecules for targeted delivery of toxin payloads into tumors. Herein we describe the discovery of BT8009, a Nectin-4 targeting BTC currently under clinical evaluation. Nectin-4 is overexpressed in multiple tumor types and is a clinically validated target for selective delivery of cytotoxic payloads. A Nectin-4 targeting bicyclic peptide was identified by phage display, which showed highly selective binding for Nectin-4 but suffered from low plasma stability and poor physicochemical properties. Multiparameter chemical optimization involving introduction of non-natural amino acids resulted in a lead Bicycle that demonstrated high affinity for Nectin-4, good stability in biological matrices, and a much-improved physicochemical profile. The optimized Bicycle was conjugated to the cytotoxin Monomethyl auristatin E via a cleavable linker to give the targeted drug conjugate BT8009, which demonstrates potent anticancer activity in in vivo rodent models.
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