化学
膨胀的
合理设计
肽
互补性(分子生物学)
纳米技术
癌症治疗
组合化学
药物发现
计算生物学
癌症研究
分子成像
内化
癌症影像学
癌症治疗
癌症
分子工程
癌症免疫疗法
转化式学习
蛋白质工程
免疫疗法
精确肿瘤学
肽合成
小分子
折叠(DSP实现)
免疫原性
靶向治疗
显像剂
癌细胞
连接器
对偶(语法数字)
新视野
肽库
放射免疫疗法
计算机科学
作者
Xueting Cheng,Shuo Jiang,X.-G. Peng,Yang Pan,Siqi Zhang,Chaoying Xu,Xin Gao,Shihui Fan,Hongtan Liu,Jie Zhuang,Xueyao Chen,Naixin Liang,Bin Lin,Qingshuang Lu,Meirong Chen,Yibei Xiao,Zhaohui Zhu,Rui Wang,Kuan Hu,Chuanliu Wu
摘要
Radiotheranostics holds transformative potential for precision oncology by integrating diagnostic imaging with targeted radionuclide therapy. However, advancements in this field are significantly hindered by the limited availability of high-affinity ligands that are capable of engaging challenging cell-surface antigens, particularly flat, low-druggability targets such as programmed death-ligand 1 (PD-L1). Here, we overcome this barrier through de novo discovery and rational engineering of a disulfide-directed multicyclic peptide (DDMP), dmp10, which achieves a picomolar affinity for PD-L1 by leveraging conformationally constrained structural scaffolds. By combining disulfide-directed library design with iterative directed evolution, we successfully generated dmp10, a ∼3 kDa multicyclic peptide that establishes unprecedented shape complementarity to the expansive binding interface of PD-L1. Preclinical evaluations demonstrated that 68Ga-labeled dmp10 enables high-contrast PET imaging of PD-L1+ tumors in murine models, achieving a tumor uptake of 13.27 %ID/g at 4 h post-injection. The therapeutic counterpart, 177Lu-labeled dmp10, effectively eradicated 92.47% of established tumors in tumor models while sparing healthy tissues, thereby validating its dual radiotheranostic utility. The translational relevance of our findings was further confirmed in a first-in-human pilot study, where 68Ga-labeled dmp10 was well tolerated and allowed visualization of PD-L1+ lesions in patients with solid tumors. This work not only establishes DDMPs as a versatile platform for targeting geometrically complex antigens but also delivers a promising radiotheranostic agent that bridges molecular imaging and precision radionuclide therapy for PD-L1-driven malignancies. Our findings advance current strategies for designing ultrahigh-affinity peptide binders and underscore the untapped potential of multicyclic architectures in overcoming longstanding challenges in cancer theranostics.
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