嵌段共聚物小泡中三维DNA折纸纳米孔的插入

IF 3.1 Q2 CHEMISTRY, MULTIDISCIPLINARY
Dr. Saskia Groeer, Dr. Martina Garni, Dr. Avik Samanta, Prof. Dr. Andreas Walther
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引用次数: 3

摘要

基于嵌段共聚物的聚合体是自下而上设计原始细胞的重要组成部分,由于其更高的机械稳定性和化学通用性,被认为比脂质体更有优势。赋予这两种类型的囊泡跨膜运输能力对于创建纳米反应器功能非常重要,并且通过插入蛋白质纳米孔来实现,即使是在相当厚的聚合体膜中。尽管如此,蛋白质纳米孔的设计空间是有限的,更高的灵活性可能通过DNA纳米孔的重新设计来实现,迄今为止,DNA纳米孔主要局限于脂质体系统。在这里,我们成功地将两种不同的3D DNA折纸纳米孔插入到PMOXA-b-PDMS-b-PMOXA聚合体中,并通过染料流入研究和显微镜证实了孔的形成。因此,这项研究为基于聚合体的功能原始细胞的多用途类大DNA折纸纳米孔的进一步设计开辟了空间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Insertion of 3D DNA Origami Nanopores into Block Copolymer Vesicles

Insertion of 3D DNA Origami Nanopores into Block Copolymer Vesicles

Block copolymer-based polymersomes are important building blocks for the bottom-up design of protocells and are considered advantageous over liposomes due to their higher mechanical stability and chemical versatility. Endowing both types of vesicles with capabilities for transmembrane transport is important for creating nanoreactor functionality and has been achieved by insertion of protein nanopores, even into comparably thick polymersome membranes. Still, the design space for protein nanopores is limited and higher flexibility might be accessible by de novo design of DNA nanopores, which have thus far been limited largely to liposome systems. Here, we introduce the successful insertion of two different 3D DNA origami nanopores into PMOXA-b-PDMS-b-PMOXA polymersomes, and confirm pore formation by dye influx studies and microscopy. This research thus opens the further design space of this versatile class of large DNA origami nanopores for polymersome-based functional protocells.

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