化学
连接器
环肽
肽
生物活性
生物物理学
立体化学
构象变化
组合化学
拟肽
血浆蛋白结合
整合素
蛋白质结构
位阻效应
分子识别
肽库
芳香性
结构母题
数量结构-活动关系
分子模型
分子动力学
结合位点
萘
肽键
结构-活动关系
细胞
分子
作者
Quan Zuo,Ximiao Yang,Junlong Lu,H Huang,Z Huang,Jie Yan,Hao Tian,Qichao He,Qichen Hu,Jieting Shen,Zirui Zhang,Qian Lü,Jiang Wu,Fang Wang,Rui Wang,Kuan Hu
标识
DOI:10.1021/acs.jmedchem.6c00693
摘要
Conformational precision is critical for peptide therapeutic design, yet the quantitative link between cross-linker geometry and in vivo performance remains unclear. We present a programmable platform using eight bi-triazine cross-linkers with varied bond length, angle, aromaticity, and symmetry to establish multilevel structure–conformation–biology relationships. Using cyclic RGD peptides targeting integrin αvβ3 and dimeric KTLLPTP peptides targeting Plectin-1 as complementary models, we integrated binding assays, cell studies, and in vivo 68Ga-PET/CT imaging to systematically evaluate linker-induced conformational effects. Two design paradigms emerged: in cyclic peptides, aromaticity and symmetry govern conformational locking, with nonmirror-symmetric naphthalene linkers enhancing protein affinity and tumor uptake. In dimeric systems, bond length and angle enable geometric matching via the “molecular ruler” effect, with a 120° benzene linker enabling optimal bivalent binding. This work not only identifies the lead candidate [68Ga]Ga-8a with high tumor contrast (∼5 %ID/mL) but also provides a generalizable framework for precision peptide engineering.
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