化学
亲缘关系
圆二色性
整合素
生物物理学
体内
结合亲和力
体外
选择性
立体化学
血浆蛋白结合
肽
生物化学
环肽
分子成像
结构母题
结合选择性
结构-活动关系
装订袋
结合位点
光学成像
蛋白质结构
生物活性
分子探针
作者
Ximiao Yang,Quan Zuo,Qichao He,H Huang,Hao Tian,Zirui Zhang,J B Yan,Rui Wang,Kuan Hu
标识
DOI:10.1021/acs.jmedchem.6c00859
摘要
Integrin-subtype selectivity remains a challenging for RGD-based imaging probes because of conserved binding interfaces among integrins. Here, we developed a conformational tuning strategy for cyclic RGD peptides by varying the carbon-spacer length and turn-inducing motifs in a 25-member library. Biolayer interferometry screening identified subtype-preferred ligands with nanomolar-level apparent affinities toward αvβ6, αvβ3, and α5β1, including 3ba/3bb/3bd, 3be, and 3bc/3dc, respectively. Circular dichroism suggested that cross-linker geometry and turn motifs modulate the RGD peptides’ secondary structure. FITC-labeled probes showed receptor-associated cellular uptake in BxPC3, A549, and U87MG cells, supporting integrin-subtype-preferred recognition at the cellular level. Furthermore, [ 68 Ga]Ga-8ba showed enhanced αvβ6-associated tumor uptake in BxPC3 xenografts, whereas [ 68 Ga]Ga-8bc and [ 68 Ga]Ga-8dc exhibited favorable α5β1-targeted imaging in U87MG tumors. The αvβ3-targeted probe retained subtype-associated recognition in vitro but showed limited tumor accumulation in vivo . These findings support conformational regulation as a viable strategy for designing subtype-selective integrin PET probes.
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