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Harnessing surface-bound enzymatic reactions to organize microcapsules in solution

机译:利用表面结合的酶促反应在溶液中组织微胶囊

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摘要

By developing new computational models, we examine how enzymatic reactions on an underlying surface can be harnessed to direct the motion and organization of reagent-laden microcapsules in a fluid-filled microchannel. In the presence of appropriate reagents, surface-bound enzymes can act as pumps, which drive large-scale fluid flows. When the reagents diffuse through the capsules’ porous shells, they can react with enzymatic sites on the bottom surface. The ensuing reaction generates fluid density variations, which result in fluid flows. These flows carry the suspended microcapsules and drive them to aggregate into “colonies” on and near the enzyme-covered sites. This aggregation continues until the reagent has been depleted and the convection stops. We show that the shape of the assembled colonies can be tailored by patterning the distribution of enzymes on the surface. This fundamental physicochemical mechanism could have played a role in the self-organization of early biological cells (protocells) and can be used to regulate the autonomous motion and targeted delivery of microcarriers in microfluidic devices.
机译:通过开发新的计算模型,我们研究了如何利用底层表面的酶促反应来指导充满液体的微通道中载有试剂的微胶囊的运动和组织。在适当的试剂存在下,表面结合的酶可以充当泵,驱动大规模的流体流动。当试剂通过胶囊的多孔壳扩散时,它们可以与底面上的酶部位发生反应。随后的反应产生流体密度变化,这导致流体流动。这些流动携带了悬浮的微胶囊,并促使它们聚集在被酶覆盖的部位上或附近的“菌落”中。这种聚集一直持续到试剂耗尽并且对流停止为止。我们表明,可以通过在表面上构图酶的分布来定制组装菌落的形状。这种基本的物理化学机制可能在早期生物细胞(原始细胞)的自组织中发挥了作用,并且可以用来调节微流体设备中微载体的自主运动和靶向递送。

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