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Integrated microfluidic chip for on-line proteome analysis with combination of denaturing and rapid digestion of protein

机译:用于在线蛋白质组分析的集成微流体芯片,与蛋白质的结合和快速消化

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摘要

A microfluidic platform based on the integration of denaturation and online immobilized enzyme reactor (IMER) digestion for protein pretreatment was first developed on a glass chip. The design of three inlet channels and two groups of snake channel in glass chip can allow the protein solution, the reducing reagent and the alkylating agent to be simultaneously injected into the chip channel and ensured the reaction solution on-line efficient mixing and sufficient reacting. By thiol-ene click chemistry, the capillary-based and glass chip-based trypsin IMER on the surface of poly(trimethylolpropane trimethacrylate) monolith were fabricated. The wide range of flow rate tolerance (0.8-5.0 mL/min), and the acceptable reproducibility (RSD% = 3.1%, n = 5) and stability (13.8% decrease of enzyme activity in 2 months) indicated the feasibility of using IMER for online digestion of proteins. Compared with the solution denaturation-offline IMER digestion, the integrated microfluidic platform of chip denaturation-chip IMER and chip denaturation-online IMER have comparable protein identification ability for mouse liver protein with a similar number of protein (798 or 826 vs. 843) and unique peptides (3923 or 4593 vs. 3916). More importantly, the easy and fast digestion of protein samples and possible combination with MS revealed that this microfluidic platform can be a potential method for rapid proteomics analysis. (C) 2020 Elsevier B.V. All rights reserved.
机译:一种基于变性和在线固定化酶反应器(IMER)消化的微流体平台首先在玻璃芯片上发育蛋白质预处理。三个入口通道的设计和玻璃芯片中的两组蛇通道可以允许蛋白质溶液,还原剂和烷基化剂同时注入芯片通道中,并确保在线有效混合和充分的反应溶液。通过Thiol-ene点击化学,制备聚(三羟甲基丙烷三丙烯酸三丙烯酸三丙烯酸三丙烯酸三丙烯酸三丙烯酸酯)表面上的基于毛细管和基于玻璃芯片的胰蛋白酶溶质。流量耐受性(0.8-5.0ml / min)和可接受的再现性(RSD%= 3.1%,n = 5)和稳定性(2个月内的酶活性降低13.8%)表明使用造皮的可行性用于在线消化蛋白质。与溶液变性 - 离线造型消化相比,芯片变性芯片造型的集成微流体平台和芯片变性 - 在线造型具有相当的蛋白质鉴定能力,具有类似数量的蛋白质(798或826与843)和独特的肽(3923或4593 vs.3916)。更重要的是,易于和快速消化的蛋白质样品和可能的与MS的组合显示,该微流体平台可以是快速蛋白质组学分析的潜在方法。 (c)2020 Elsevier B.V.保留所有权利。

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