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用于基质辅助激光解吸电离飞行时间质谱的自动化消化与液滴沉积微流控芯片的开发。

Development of an automated digestion and droplet deposition microfluidic chip for MALDI-TOF MS.

作者信息

Lee Jeonghoon, Musyimi Harrison K, Soper Steven A, Murray Kermit K

机构信息

Department of Chemistry, Louisiana State University, Baton Rouge, Louisiana 70802, USA.

出版信息

J Am Soc Mass Spectrom. 2008 Jul;19(7):964-72. doi: 10.1016/j.jasms.2008.03.015. Epub 2008 Apr 8.

Abstract

An automated proteolytic digestion bioreactor and droplet deposition system was constructed with a plastic microfluidic device for off-line interfacing to matrix assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). The microfluidic chips were fabricated in poly(methyl methacrylate) (PMMA), using a micromilling machine and incorporated a bioreactor, which was 100 microm wide, 100 microm deep, and possessed a 4 cm effective channel length (400 nL volume). The chip was operated by pressure-driven flow and mounted on a robotic fraction collector system. The PMMA bioreactor contained surface immobilized trypsin, which was covalently attached to the UV-modified PMMA surface using coupling reagents N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC) and hydroxysulfosuccinimide (sulfo-NHS). The digested peptides were mixed with a MALDI matrix on-chip and deposited as discrete spots on MALDI targets. The bioreactor provided efficient digestion of a test protein, cytochrome c, at a flow rate of 1 microL/min, producing a reaction time of approximately 24 s to give adequate sequence coverage for protein identification. Other proteins were also evaluated using this solid-phase bioreactor. The efficiency of digestion was evaluated by monitoring the sequence coverage, which was 64%, 35%, 58%, and 47% for cytochrome c, bovine serum albumin (BSA), myoglobin, and phosphorylase b, respectively.

摘要

构建了一种自动化蛋白水解消化生物反应器和液滴沉积系统,该系统采用塑料微流控装置,用于与基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)进行离线连接。微流控芯片由聚甲基丙烯酸甲酯(PMMA)制成,使用微铣床制造,并集成了一个生物反应器,该生物反应器宽100微米,深100微米,有效通道长度为4厘米(体积为400纳升)。芯片通过压力驱动流操作,并安装在机器人馏分收集器系统上。PMMA生物反应器含有表面固定化的胰蛋白酶,使用偶联试剂N-(3-二甲基氨基丙基)-N'-乙基碳二亚胺盐酸盐(EDC)和羟基磺基琥珀酰亚胺(磺基-NHS)将其共价连接到经紫外线改性的PMMA表面。消化后的肽在芯片上与MALDI基质混合,并作为离散斑点沉积在MALDI靶上。该生物反应器以1微升/分钟的流速对测试蛋白细胞色素c进行了高效消化,产生了约24秒的反应时间,以提供足够的序列覆盖率用于蛋白质鉴定。还使用该固相生物反应器对其他蛋白质进行了评估。通过监测序列覆盖率来评估消化效率,细胞色素c、牛血清白蛋白(BSA)、肌红蛋白和磷酸化酶b的序列覆盖率分别为64%、35%、58%和47%。

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