Insertion of 3D DNA Origami Nanopores into Block Copolymer Vesicles

被引:5
|
作者
Groeer, Saskia [1 ,2 ,3 ]
Garni, Martina [4 ]
Samanta, Avik [6 ]
Walther, Andreas [5 ,6 ]
机构
[1] Univ Freiburg, Inst Macromol Chem, A3BMS Lab Act Adapt & Autonomous Bioinspired Mat, Stefan Meier Str 3, D-79104 Freiburg, Germany
[2] Univ Freiburg, Freiburg Mat Res Ctr FMF, Stefan Meier Str 21, D-79104 Freiburg, Germany
[3] Univ Freiburg, Freiburg Ctr Interact Mat & Bioinspired Technol F, Georges Kohler Allee 105, D-79110 Freiburg, Germany
[4] Univ Basel, Chem Dept, BPR 1096,Postfach 3350,Mattenstr 24a, CH-4002 Basel, Switzerland
[5] Cluster Excellence LivMatS FIT, D-79110 Freiburg, Germany
[6] Johannes Gutenberg Univ Mainz, Dept Chem, A3BMS Lab Act Adapt & Autonomous Bioinspired Mat, D-55128 Mainz, Germany
基金
欧洲研究理事会; 瑞士国家科学基金会;
关键词
Artificial cells; DNA origami; nanopores; vesicles; polymersomes; POLYMER MEMBRANES; NANOCOMPARTMENTS; PERMEABILITY; PROTEINS; DYNAMICS; CHANNELS;
D O I
10.1002/syst.202200009
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页数:7
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