杯芳烃
两亲性
化学
烷基
阳离子聚合
肽
胶束
组合化学
内化
自组装
有机化学
水溶液
分子
生物化学
共聚物
受体
聚合物
作者
R. V. Rodik,S. О. Cherenok,Viktoriia Postupalenko,Sule Oncul,Vladyslava Brusianska,Petro Borysko,Vitaly I. Kаlchеnkо,Yves Mély,Andrey S. Klymchenko
标识
DOI:10.1016/j.jcis.2022.05.124
摘要
Shape-persistent macrocycles enable superior control on molecular self-assembly, allowing the preparation of well-defined nanostructures with new functions. Here, we report on anionic amphiphilic calixarenes of conic shape and their self-assembly behavior in aqueous media for application in intracellular delivery of peptides. Newly synthesized calixarenes bearing four phosphonate groups and two or four long alkyl chains were found to form micelles of ∼ 10 nm diameter, in contrast to an analogue with short alkyl chains. These amphiphilic calixarenes are able to complex model (oligo-lysine) and biologically relevant (HIV-1 nucleocapsid peptide) cationic peptides into small nanoparticles (20-40 nm). By contrast, a control anionic calixarene with short alkyl chains fails to form small nanoparticles with peptides, highlighting the importance of micellar assembly of amphiphilic calixarenes for peptide complexation. Cellular studies reveal that anionic amphiphilic calixarenes exhibit low cytotoxicity and enable internalization of fluorescently labelled peptides into live cells. These findings suggest anionic amphiphilic macrocycles as promising building blocks for the preparation of peptide delivery vehicles.
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