Shanghai Key Laboratory of Advanced Polymeric Materials, State Key Laboratory of Bioreactor Engineering, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology , Shanghai 200237, China.
Langmuir. 2016 Jul 12;32(27):6917-27. doi: 10.1021/acs.langmuir.6b01484. Epub 2016 Jun 27.
Cooperative self-assembly behavior of rod-coil-rod poly(γ-benzyl-l-glutamate)-block-poly(ethylene glycol)-block-poly(γ-benzyl-l-glutamate) (PBLG-b-PEG-b-PBLG) amphiphilic triblock copolymers and hydrophobic gold nanoparticles (AuNPs) was investigated by both experiments and dissipative particle dynamics (DPD) simulations. It was discovered that pure PBLG-b-PEG-b-PBLG copolymers self-assemble into ellipse-like aggregates, and the morphology transforms into vesicles as AuNPs are introduced. When the hydrophobicity of AuNPs is close to that of the copolymers, AuNPs are homogeneously distributed in the vesicle wall. While for the AuNPs with higher hydrophobicity, they are embedded in the vesicle wall as clusters. In addition to the experimental observations, DPD simulations were performed on the self-assembly behavior of triblock copolymer/nanoparticle mixtures. Simulations well reproduced the morphology transition observed in the experiments and provided additional information such as chain packing mode in aggregates. It is deduced that the main reason for the ellipse-to-vesicle transition of the aggregates is attributed to the breakage of ordered and dense packing of PBLG rods in the aggregate core by encapsulating AuNPs. This study deepens our understanding of the self-assembly behavior of rod-coil copolymer/nanoparticle mixtures and provides strategy for designing hybrid polypeptide nanostructures.
两亲性三嵌段共聚物聚(γ-苄基-L-谷氨酸酯)-嵌段-聚乙二醇-嵌段-聚(γ-苄基-L-谷氨酸酯)(PBLG-b-PEG-b-PBLG)与疏水金纳米粒子(AuNPs)的协同自组装行为通过实验和耗散粒子动力学(DPD)模拟进行了研究。结果发现,纯 PBLG-b-PEG-b-PBLG 共聚物自组装成椭圆形聚集体,当引入 AuNPs 时,形态转变为囊泡。当 AuNPs 的疏水性接近共聚物时,AuNPs 均匀分布在囊泡壁中。而对于疏水性更高的 AuNPs,它们则以簇的形式嵌入囊泡壁中。除了实验观察外,还对三嵌段共聚物/纳米粒子混合物的自组装行为进行了 DPD 模拟。模拟很好地再现了实验中观察到的形态转变,并提供了聚集体内链组装模式等附加信息。推断聚集体的椭圆到囊泡的转变的主要原因是通过封装 AuNPs 破坏了聚集核中 PBLG 棒的有序和密集堆积。这项研究加深了我们对棒-线共聚物/纳米粒子混合物自组装行为的理解,并为设计杂化多肽纳米结构提供了策略。