Yan Qiang, Zhang Hongji, Zhao Yue
Département de Chimie, Université de Sherbrooke, Sherbrooke, Québec J1K 2R1, Canada.
ACS Macro Lett. 2014 May 20;3(5):472-476. doi: 10.1021/mz500181q. Epub 2014 May 6.
A novel supramolecular block glycopolypeptide, designed to have the viral building blocks and be sensitive to CO, a physiological stimulus, was prepared via the orthogonal coupling of two end-functionalized biopolymers, dextran with β-cyclodextrin terminal (Dex-CD) and poly(l-valine) with a benzimidazole tail (BzI-PVal), respectively, driven by the end-to-end host-guest interactions. Due to the CO-cleavable CD/BzI connection, both the vesicular and fibrous aggregates of this supramolecular block copolymer self-assembled in aqueous solution can undergo a reversible process of disassembly upon "breathing in" CO and assembly upon "breathing out" CO, which mimics, to some extent, the disintegration and construction of viral capsid nanostructures.
通过分别由端对端主客体相互作用驱动的两种末端功能化生物聚合物——β-环糊精末端的右旋糖酐(Dex-CD)和带有苯并咪唑尾的聚(L-缬氨酸)(BzI-PVal)的正交偶联,制备了一种新型超分子嵌段糖多肽。该超分子嵌段糖多肽被设计成具有病毒构建块且对生理刺激物一氧化碳(CO)敏感。由于CO可裂解的CD/BzI连接,这种超分子嵌段共聚物在水溶液中自组装形成的囊泡状和纤维状聚集体在“吸入”CO时均可经历可逆的解体过程,在“呼出”CO时则经历组装过程,这在一定程度上模拟了病毒衣壳纳米结构的解体和构建。