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Continuous-Flow pI-Based Sorting of Proteins and Peptides in a Microfluidic Chip Using Diffusion Potential

机译:基于扩散电位的微流芯片中基于连续流动pI的蛋白质和肽的排序

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摘要

Efficient sample preparation tools are the key to measuring molecular signals in a complex biological system. A novel continuous-flow isoelectric point (pI)-based sorting technique has been developed for proteins and peptides in a microfluidic chip format. It can sort biomolecules at a relatively high flow rate of up to 10 (mu)L/min and does not require carrier ampholytes, which can create molecular backgrounds for subsequent analysis. Furthermore, the electrophoretic field required to run the pI-based sorting is generated by the diffusion of buffer ions in situ, at the liquid junction between two laminar flows within the microfluidic channel. Utilizing the diffusion potential in combination with a pH difference between the buffers, we demonstrated a separation of binary mixtures of pI markers and proteins without applying any external field. The sorting resolution and its efficiency are sufficiently high for sample preparation and could be further improved by optimizing buffers or with an additional transverse electric field. Once fully developed, it can potentially be a pI-based sample fractionation tool for proteomic analysis of complex biomolecule samples.
机译:高效的样品制备工具是在复杂的生物系统中测量分子信号的关键。已经开发了一种基于连续流等电点(pI)的新型分选技术,用于微流控芯片形式的蛋白质和肽。它可以以高达10μL/ min的相对较高的流速分选生物分子,并且不需要载体两性电解质,这可以为后续分析创造分子背景。此外,运行基于pI的分选所需的电泳场是通过缓冲液离子在微流通道内两个层流之间的液接处的原位扩散而产生的。利用扩散潜能与缓冲液之间的pH值相结合,我们证明了在不施加任何外部电场的情况下,可以分离pI标记物和蛋白质的二元混合物。分类分辨率及其效率对于样品制备而言足够高,并且可以通过优化缓冲液或使用额外的横向电场来进一步提高。一旦完全开发,它就有可能成为基于pI的样品分级工具,用于复杂生物分子样品的蛋白质组学分析。

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