An intercompartmental enzymatic cascade reaction in channel-equipped polymersome-in-polymersome architectures

被引:48
作者
Siti, Winna [1 ]
de Hoog, Hans-Peter M. [2 ]
Fischer, Ozana [3 ]
Shan, Wong Yee [4 ]
Tomczak, Nikodem [2 ]
Nallani, Madhavan [1 ]
Liedberg, Bo [1 ]
机构
[1] Nanyang Technol Univ, Sch Mat Sci & Engn, Ctr Biomimet Sensor Sci, Singapore 637553, Singapore
[2] ASTAR, Inst Mat Res & Engn, Singapore 117602, Singapore
[3] Univ Basel, Dept Chem, CH-4056 Basel, Switzerland
[4] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
关键词
MEMBRANE-PROTEIN; VESICLES; COMPARTMENTS; NANOREACTORS; DEPOSITION; LIPOSOMES; RELEASE; ENZYMES; SYSTEMS;
D O I
10.1039/c3tb21849j
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Compartmentalization, as a design principle, is a prerequisite for the functioning of eukaryotic cells. Although cell mimics in the form of single vesicular compartments such as liposomes or polymersomes have been tremendously successful, investigations of the corresponding higher-order architectures, in particular bilayer-based multicompartment vesicles, have only recently gained attention. We hereby demonstrate a multicompartment cell-mimetic nanocontainer, built-up from fully synthetic membranes, which features an inner compartment equipped with a channel protein and a semi-permeable outer compartment that allows passive diffusion of small molecules. The functionality of this multicompartment architecture is demonstrated by a cascade reaction between enzymes that are segregated in separate compartments. The unique architecture of polymersomes, which combines stability with a cell-membrane-mimetic environment, and their assembly into higher-order architectures could serve as a design principle for new generation drug-delivery vehicles, biosensors, and protocell models.
引用
收藏
页码:2733 / 2737
页数:5
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