Development of a Thiol–ene Microfluidic Chip for Hydrogen/Deuterium Exchange Mass Spectrometry (HDX-MS)

IF 6.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Anton B. Hansen, Rasmus R. Svejdal, Jordan T. Aerts, Vanessa B. P. Stahlhut, Daria Harmash, Minna Hamidi, Drago Sticker, Jörg P. Kutter and Kasper D. Rand*, 
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Abstract

Hydrogen/deuterium exchange mass spectrometry (HDX-MS) is a powerful technique for analyzing the conformational dynamics of proteins. Using liquid chromatography coupled to mass spectrometry (LC-MS), the method achieves high sensitivity and the option to measure the HDX either of the intact protein (global analysis) or of small peptide segments of the protein (local analysis) after online pepsin proteolysis. However, HDX-MS is currently limited by the significant cost of the specialized refrigerated UPLC-based chromatographic equipment needed and by the loss of deuterium label from the analyzed protein (30–50%), which still occurs despite cooling parts of the LC-MS system to 0 °C. Here we describe the development of a microfluidic chip (HDXchip) for global or local HDX-MS analysis that can be cooled to subzero temperatures. HDXchip comprises a sample loading module with an immobilized enzyme microreactor (IMER) for on-chip pepsin proteolysis and a module packed with reversed-phase material for on-chip desalting and reversed-phase chromatography. The chip thus integrates the hallmarks of the classical HDX-MS workflow in a low-cost, low-volume microfluidic format. Furthermore, the small size of the chip allows for efficient localized cooling of parts of the chip to subzero temperatures by a Peltier module. We show that HDXchip allows for HDX-MS analysis of model peptides and intact proteins at significantly lowered back-exchange compared to a conventional commercially available UPLC-based HDX-MS setup. Furthermore, we show that the chip is capable of local HDX-MS analysis of hemoglobin with good sensitivity, sequence coverage, repeatability, and low back-exchange. Our results demonstrate the potential of integrating the HDX-MS workflow, including proteolysis and separation, with subzero temperature cooling, on a microchip.

Abstract Image

氢/氘交换质谱(HDX-MS)用巯基微流控芯片的研制
氢/氘交换质谱(HDX-MS)是一种分析蛋白质构象动力学的强大技术。使用液相色谱-质谱联用(LC-MS),该方法实现了高灵敏度,并且可以选择在线胃蛋白酶蛋白水解后测量完整蛋白(全局分析)或蛋白质小肽段(局部分析)的HDX。然而,HDX-MS目前受限于所需的专用冷藏uplc色谱设备的巨大成本,以及分析蛋白质中氘标签的损失(30-50%),尽管LC-MS系统的部分冷却到0°C仍会发生这种情况。在这里,我们描述了用于全局或局部HDX-MS分析的微流控芯片(HDXchip)的开发,该芯片可以冷却到零度以下的温度。HDXchip包括一个带有固定化酶微反应器(IMER)的样品上样模块,用于片上胃蛋白酶蛋白水解;一个装有反相材料的模块,用于片上脱盐和反相色谱。因此,该芯片集成了经典HDX-MS工作流程的特点,以低成本,小体积的微流控格式。此外,芯片的小尺寸允许通过Peltier模块有效地局部冷却芯片部分到零度以下的温度。我们发现,与传统的市售uplc为基础的HDX-MS设置相比,HDXchip允许HDX-MS分析模型肽和完整蛋白质的回交换显著降低。此外,我们表明该芯片能够进行血红蛋白的局部HDX-MS分析,具有良好的灵敏度、序列覆盖率、可重复性和低回交换。我们的研究结果证明了将HDX-MS工作流程(包括蛋白水解和分离)与零下温度冷却集成到微芯片上的潜力。
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来源期刊
Analytical Chemistry
Analytical Chemistry 化学-分析化学
CiteScore
12.10
自引率
12.20%
发文量
1949
审稿时长
1.4 months
期刊介绍: Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.
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