首页> 外文期刊>Journal of physical chemistry letters >Highly Stable, Ultrasmall Polymer-Grafted Nanobins (usPGNs) with Stimuli-Responsive Capability
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Highly Stable, Ultrasmall Polymer-Grafted Nanobins (usPGNs) with Stimuli-Responsive Capability

机译:具有刺激响应能力的高度稳定,超强聚合物接枝纳米蛋白(USPGNS)

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Highly stable and stimuli/pH-responsive ultrasmall polymer-grafted nanobins (usPGNs) have been developed by grafting a small amount (10 mol %) of short (4.3 kDa) cholesterol-terminated poly(acrylic acid) (Chol-PAA) into an ultrasmall unilamellar vesicle (uSUV). The usPGNs are stable against fusion and aggregation over several weeks, exhibiting over 10-fold enhanced cargo retention in biologically relevant media at pH 7.4 in comparison with the parent uSUV template. Coarse-grained molecular dynamics (CGMD) simulations confirm that the presence of the cholesterol moiety can greatly stabilize the lipid bilayer. They also show extended PAA chain conformations that can be interpreted as causing repulsion between colloidal particles, thus stabilizing them against fusion. Notably, CGMD predicted a clustering of the Chol-PAA chains on the lipid bilayer under acidic conditions due to intra- and interchain hydrogen bonding, leading to the destabilization of local membrane areas. This explains the experimental observation that usPGNs can be triggered to release a significant amount of cargo upon acidification to pH 5. These developments put the lipid-bilayer-embedded Chol-PAA in stark contrast with traditional poly(acrylic acid) systems where the molar mass (M-n) of the polymer chains must exceed 16.5 kDa to achieve stimuli-responsive changes in conformation. They also distinguish the small usPGNs from the much-larger polymer-caged nanobin platform where the Chol-PAA chains must be covalently cross-linked to engender stimuli-responsive behaviors.
机译:通过将少量(10mol%)的短(4.3kDa)胆固醇封端的聚(丙烯酸)(Chol-Paa)嫁接成一个UltraMall Unilamellar囊泡(USUV)。 USPGNS在几周内对融合和聚集稳定,与母体USUV模板相比,在pH 7.4的生物相关培养基中表现出超过10倍的货物保留。粗粒化分子动力学(CGMD)模拟证实,胆固醇部分的存在可以大大稳定脂质双层。它们还显示了可以解释为胶体颗粒之间的排斥的扩展PAA链构象,从而稳定它们反对融合。值得注意的是,CGMD由于内部氢键引起的酸性条件下,CGMD预测了脂质双层对脂质双层的聚类,导致局部膜区域的稳定化。这解释了实验观察,即可以触发USPGNS以释放酸化至pH的含量大量货物5.这些发育使脂质双层嵌入式乳酸Paa与摩尔质量的传统聚(丙烯酸)系统进行瘙痒症对比聚合物链的(Mn)必须超过16.5kDa,以实现刺激反应的构象变化。它们还将小USPGN与大多数较大的聚合物笼式纳米蛋白平台区分开,其中核PAA链必须共价交联以获得刺激敏敏的行为。

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