生物正交化学
化学
蛋白质降解
前药
降级(电信)
四嗪
癌细胞
细胞
癌症研究
肿瘤细胞
靶蛋白
癌症
癌症治疗
分子成像
纳米探针
结合
纳米技术
生物化学
蛋白质-蛋白质相互作用
作者
Feilong Sun,Tian Wang,Pengfei Wang,Jiaxin Shi,Yanyan Shen,Guilong Wang,Biyu Yang,Huiwen Li,Qiumeng Zhang,Yi Chen,Xuan Zhang
摘要
Targeted protein degradation offers therapeutic promise but often suffers from on-target off-tissue toxicities. To overcome this challenge, we developed a versatile theranostic platform that integrates tumor cell imaging with precisely controlled protein degradation. Central to this platform is XZ2223, a glutathione (GSH)-cleavable bioorthogonal trigger that couples cancer cell labeling with concomitant tetrazine release, thereby activating trans-cyclooctene (TCO)-caged CRBN-recruiting degrader prodrugs, Pro-CC-885 and Pro-dBET6, to induce on-demand degradation of GSPT1 and BET, respectively. Coadministration of XZ2223 with either prodrug afforded robust tumor imaging and efficient protein degradation in xenograft models, while the XZ2223/Pro-dBET6 combination further elicited in vivo antitumor efficacy with reduced systemic toxicity. This innovative platform shows potential as a dual-function approach for precision cancer therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI