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聚合物囊泡在“凝胶状”聚合物囊泡中:向结构细胞模拟迈进。

Polymersomes in "gelly" polymersomes: toward structural cell mimicry.

机构信息

Université de Bordeaux /IPB, ENSCBP, 16 avenue Pey Berland, 33607 Pessac Cedex, France.

出版信息

Langmuir. 2012 Jan 31;28(4):2035-43. doi: 10.1021/la204018w. Epub 2011 Dec 23.

Abstract

We demonstrate here the formation of compartmentalized polymersomes with an internal "gelly" cavity using an original and versatile process. Nanosize polymersomes of poly(trimethylene carbonate)-b-poly(L-glutamic acid) (PTMC-b-PGA), formed by a solvent displacement method are encapsulated with a rough "cytoplasm mimic" in giant polymersomes of poly(butadiene)-b-poly(ethylene oxide) PB-b-PEO by emulsion-centrifugation. Such a system constitutes a first step toward the challenge of structural cell mimicry with both "organelles" and "cytoplasm mimics". The structure is demonstrated with fluorescence labeling and confocal microscopy imaging with movies featuring the motion of the inner nanosize polymersomes in larger vesicles. Without "cytoplasm mimic", the motion was confirmed to be Brownian by particle tracking analysis. The inner nanosize polymersomes motion was blocked in the presence of alginate, but only hindered in the presence of dextran. With the use of such high molecular weight and concentrated polysaccharides, the crowded internal volume of cells, responsible for the so-called "macromolecular crowding" effect influencing every intracellular macromolecular association, seems to be efficiently mimicked. This study constitutes major progress in the field of structural biomimicry and will certainly enable the rise of new, highly interesting properties in the field of high-added value soft matter.

摘要

我们在这里展示了一种使用原始且通用的方法形成具有内部“凝胶”腔的分隔聚合物囊泡的方法。通过溶剂置换法形成的聚(三亚甲基碳酸酯)-b-聚(L-谷氨酸)(PTMC-b-PGA)纳米尺寸聚合物囊泡通过乳液离心被包封在聚丁二烯)-b-聚(氧化乙烯)(PB-b-PEO)的巨大聚合物囊泡中的粗糙“细胞质模拟物”中。这样的系统构成了朝着具有“细胞器”和“细胞质模拟物”的结构细胞模拟的挑战迈出的第一步。荧光标记和共焦显微镜成像以及带有内部纳米尺寸聚合物囊泡在较大囊泡中运动的电影显示了该结构。在没有“细胞质模拟物”的情况下,通过粒子跟踪分析证实了运动是布朗运动。在存在藻酸盐的情况下,内部纳米尺寸聚合物囊泡的运动被阻断,但在存在葡聚糖的情况下,仅被阻碍。使用这种高分子量和高浓度的多糖,可以有效地模拟细胞内部拥挤的体积,这是导致所谓的“大分子拥挤”效应的原因,该效应影响每个细胞内大分子的相互作用。这项研究在结构仿生学领域取得了重大进展,必将在高附加值软物质领域带来新的、非常有趣的性质。

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