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Sequential Release of Proteins from Structured Multishell Microcapsules

机译:来自结构化Mulishell微胶囊的蛋白质的顺序释放

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摘要

In nature, a wide range of functional materials is based on proteins. Increasing attention is also turning to the use of proteins as artificial biomaterials in the form of films, gels, particles, and fibrils that offer great potential for applications in areas ranging from molecular medicine to materials science. To date, however, most such applications have been limited to single component materials despite the fact that their natural analogues are composed of multiple types of proteins with a variety of functionalities that are coassembled in a highly organized manner on the micrometer scale, a process that is currently challenging to achieve in the laboratory. Here, we demonstrate the fabrication of multicomponent protein microcapsules where the different components are positioned in a controlled manner. We use molecular self-assembly to generate multicomponent structures on the nanometer scale and droplet microfluidics to bring together the different components on the micrometer scale. Using this approach, we synthesize a wide range of multiprotein microcapsules containing three well-characterized proteins: glucagon, insulin, and lysozyme. The localization of each protein component in multishell microcapsules has been detected by labeling protein molecules with different fluorophores, and the final three-dimensional microcapsule structure has been resolved by using confocal microscopy together with image analysis techniques. In addition, we show that these structures can be used to tailor the release of such functional proteins in a sequential manner. Moreover, our observations demonstrate that the protein release mechanism from multishell capsules is driven by the kinetic control of mass transport of the cargo and by the dissolution of the shells. The ability to generate artificial materials that incorporate a variety of different proteins with distinct functionalities increases the breadth of the potential applications of artificial protein-based materials and provides opportunities to design more refined functional protein delivery systems.
机译:本质上,各种功能材料基于蛋白质。越来越关注的是在薄膜,凝胶,颗粒和原纤维中的形式转向使用蛋白质作为人造生物材料,这些原因是在从分子医学到材料科学的范围内的应用中提供巨大潜力。然而,迄今为止,大多数此类应用程序仅限于单一组件材料,尽管它们的天然类似物由多种类型的蛋白质组成,具有各种功能,其在微米级上以高度有组织的方式共用,这是一种过程目前在实验室实现挑战。这里,我们证明了不同组分以受控方式定位的多组分蛋白质微胶囊的制造。我们使用分子自组装在纳米级和液滴微流体上产生多组分结构,以将不同的组分放在微米级上。使用这种方法,我们合成含有三种特征的蛋白质:胰胰高血糖素,胰岛素和溶菌酶的多种多蛋白微胶囊。通过用不同荧光团标记蛋白质分子检测多蛋白质组分在多胶囊中的定位,通过使用共聚焦显微镜以及图像分析技术,已经解决了最终的三维微胶囊结构。此外,我们表明这些结构可用于以顺序方式定制这种功能蛋白的释放。此外,我们的观察结果表明,来自多机器胶囊的蛋白质释放机理由货物的大规模运输和壳体的溶解来驱动。产生具有不同功能的各种不同蛋白质的人造材料的能力增加了人造蛋白质的材料潜在应用的宽度,并提供了设计更精细的功能蛋白输送系统的机会。

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