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A Hierarchical Assembly Process to Engineer a Hydrophobic Core for Virus-like Particles

机译:设计用于病毒样颗粒的疏水核的分层组装过程

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摘要

Modern gene- and drug-delivery vehicles are evolving into elaborate machines with multiple targeting moieties and efficient cargo-loading capacities. These functionalities need to be localized such that the targeting motifs are on the exterior with high surface accessibility whereas the cargo is protected in the interior. To address this need for incorporating a variety of functionalities with spatial selectivity, multivalent protein assemblies, viruses, and virus-like particles (VLPs) have recently been considered as ideal scaffolds. The advantages of viral systems include simple production, uniform size and structure, and a surface, which molecular cloning and protein-conjugation strategies, can display a variety of functional groups with molecular precision. In the past decade, myriad viruses and VLPs have been genetically and chemically reprogrammed to function as drug/gene-delivery vehicles, vaccine carriers, imaging probes, and composite materials.
机译:现代的基因和药物递送工具正在发展成为具有多个靶向部分和高效货物装载能力的精致机器。这些功能需要本地化,以使目标图案位于外部且具有较高的表面可及性,而货物则在内部受到保护。为了满足将各种功能与空间选择性结合在一起的需求,近来多价蛋白装配体,病毒和病毒样颗粒(VLP)被认为是理想的支架。病毒系统的优势包括生产简单,大小和结构均一以及表面,分子克隆和蛋白质结合策略可以显示出具有分子精度的各种官能团。在过去的十年中,对无数病毒和VLP进行了基因和化学重编程,以用作药物/基因传递载体,疫苗载体,成像探针和复合材料。

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