化学
内化
内吞作用
肽
前药
RGD基序
点击化学
去肽
细胞毒性
细胞培养
共焦显微镜
生物化学
立体化学
体外
整合素
组合化学
细胞
细胞生物学
生物
遗传学
作者
Markus Nahrwold,Christine Weiß,Tobias Bogner,Felix Mertink,Jens Conradi,Benedikt Sammet,Ralf Palmisano,Soledad Royo Gracia,Thomas Preuße,Norbert Sewald
摘要
Tumor targeting anticancer drug conjugates that contain a tumor recognition motif (homing device) are of high current relevance. Cryptophycins, naturally occurring cytotoxic cyclo-depsipeptides, have been modified by total synthesis to provide analogues suitable for conjugation to peptide-based homing devices. An array of functionalized β(2)-amino acids was synthesized and incorporated into cryptophycins. All analogues proved to be highly active in the cytotoxicity assay using the human cervix carcinoma cell line KB-3-1 and its multidrug-resistant subclone KB-V1. Conformational analysis of cryptophycin-52 and two synthetic analogues was performed by NMR and MD methods to obtain information on the influence of the unit C configuration on the overall conformation. An azide-functionalized cryptophycin was connected by CuAAC to an alkyne-containing fluorescently labeled cyclic RGD-peptide as the homing device for internalization studies. Confocal fluorescence microscopy proved integrin-mediated internalization by endocytosis and final lysosomal localization of the cryptophycin prodrug.
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