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基于多金属氧酸盐介导的膜组装的凝聚层基原细胞中的自发结构形成。

Spontaneous structuration in coacervate-based protocells by polyoxometalate-mediated membrane assembly.

机构信息

Centre for Organized Matter Chemistry, School of Chemistry, University of Bristol, Bristol, BS8 1TS, UK.

出版信息

Small. 2014 May 14;10(9):1830-40. doi: 10.1002/smll.201303654. Epub 2014 Feb 10.

Abstract

Molecularly crowded, polyelectrolyte/ribonucleotide-enriched membrane-free coacervate droplets are transformed into membrane-bounded sub-divided vesicles by using a polyoxometalate-mediated surface-templating procedure. The coacervate to vesicle transition results in reconstruction of the coacervate micro-droplets into novel three-tiered micro-compartments comprising a semi-permeable negatively charged polyoxometalate/polyelectrolyte outer membrane, a sub-membrane coacervate shell, and an internal aqueous lumen. We demonstrate that organic dyes, ssDNA, magnetic nanoparticles and enzymes can be concentrated into the interior of the micro-compartments by sequestration into the coacervate micro-droplets prior to vesicle formation. The vesicle-encapsulated proteins are inaccessible to proteases in the external medium, and can be exploited for the spatial localization and coupling of two-enzyme cascade reactions within single or between multiple populations of hybrid vesicles dispersed in aqueous media.

摘要

通过使用多金属氧酸盐介导的表面模板程序,将分子拥挤的聚电解质/核糖核苷酸富集的无膜凝聚液滴转化为具有膜的细分囊泡。凝聚物到囊泡的转变导致凝聚微滴重建为新型的三层微隔室,包括半透性带负电荷的多金属氧酸盐/聚电解质外层膜、亚膜凝聚壳和内部水腔。我们证明,有机染料、ssDNA、磁性纳米粒子和酶可以在囊泡形成之前通过被隔离到凝聚微滴中来浓缩到微隔室的内部。囊泡包封的蛋白质对外部介质中的蛋白酶不可接近,并且可以用于在单个或多个混合囊泡群体在水介质中分散时,在空间上定位和偶联两种酶级联反应。

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