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Microchip Protein Separartion by Electric Field Gradient Focusing

机译:通过电场梯度聚焦的微芯片蛋白分离

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摘要

A microfluidic chip is presented, which separates and focuses charged proteins based on variable electric field. The device operates by physical means involving the independent manipulation of the electrophoretic and electroosmotic forces and velocities in the channel. While electroosmosis is kept constant along the channel, the opposing electrophoretic force varies from one region to another. By this means, the net force on a given protein molecule becomes zero at a unique point while all other solutes are swept away. Like isoelectric focusing, this method concentrates separated molecules into spatially distinct bands. For injection-based methods of separation, the maximum separable quantity of solute is limited by the amount initially present in a single discrete injection plug. In contrast, the stationary zone method investigated here is capable in principle of continuous separation and accumulation up to steric and electrostatic limits. This is of potential benefit in the separation and detection of medicallyimportant trace proteins and metabolites. In this report we present experimental results describing the separation of a binary mixture of bovine serum albumin and phycoerythrin utilizing a chip comprised of intersecting channels in PDMS inlaid with hollow fibers. The results are rationalized by theory and numerical simulations.
机译:提出了一种微流体芯片,其分离并聚焦基于可变电场的带电蛋白质。该装置通过物理装置操作,涉及独立于电泳和电渗力和通道中的速度的独立操纵。虽然电渗沿着通道保持恒定,但相反的电泳力从一个区域变化到另一个区域。通过这种方式,给定蛋白质分子上的净力在独特的点处变为零,而所有其他溶质都被扫除。与等电聚焦一样,该方法将分离的分子浓缩成空间不同的带。对于基于注射的分离方法,最大可分离量的溶质量受到最初存在于单个离散注射塞中的量的限制。相反,此处研究的静止区域方法能够在连续分离和积累到空间和静电限制的原则上能够。这对杂散痕量蛋白和代谢物分离和检测具有潜在的益处。在本报告中,我们呈现了利用中空纤维中的PDMS中的交叉通道分离牛血清白蛋白和Phycoerythrin分离的实验结果。结果通过理论和数值模拟合理化。

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