Hansen Anton B, Svejdal Rasmus R, Aerts Jordan T, Stahlhut Vanessa B P, Harmash Daria, Hamidi Minna, Sticker Drago, Kutter Jörg P, Rand Kasper D
Protein Analysis Group, Department of Pharmacy, University of Copenhagen, Copenhagen 2100, Denmark.
Department of Pharmacy, University of Copenhagen, Copenhagen 2100, Denmark.
Anal Chem. 2025 Jun 24;97(24):12503-12512. doi: 10.1021/acs.analchem.4c06230. Epub 2025 Jun 9.
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 () for global or local HDX-MS analysis that can be cooled to subzero temperatures. 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 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.
氢/氘交换质谱法(HDX-MS)是一种用于分析蛋白质构象动力学的强大技术。该方法通过液相色谱与质谱联用(LC-MS),实现了高灵敏度,并可选择在在线胃蛋白酶蛋白水解后,对完整蛋白质进行氢/氘交换测量(整体分析)或对蛋白质的小肽段进行氢/氘交换测量(局部分析)。然而,目前HDX-MS受到所需的基于超高效液相色谱(UPLC)的专用冷藏色谱设备的高昂成本以及被分析蛋白质中氘标记的损失(30%-50%)的限制,尽管将LC-MS系统的部分部件冷却至0°C,这种损失仍然会发生。在此,我们描述了一种用于整体或局部HDX-MS分析的微流控芯片的开发,该芯片可冷却至零下温度。该芯片包括一个带有固定化酶微反应器(IMER)的样品加载模块,用于芯片上的胃蛋白酶蛋白水解,以及一个填充有反相材料的模块,用于芯片上的脱盐和反相色谱。因此,该芯片以低成本、小体积的微流控形式集成了经典HDX-MS工作流程的特点。此外,芯片的小尺寸使得通过珀耳帖模块能够有效地将芯片的部分区域局部冷却至零下温度。我们表明,与传统的基于商业UPLC的HDX-MS装置相比,该芯片能够在显著降低的回交换情况下对模型肽和完整蛋白质进行HDX-MS分析。此外,我们表明该芯片能够以良好的灵敏度、序列覆盖率、重复性和低回交换对血红蛋白进行局部HDX-MS分析。我们的结果证明了在微芯片上集成HDX-MS工作流程(包括蛋白水解和分离)以及零下温度冷却的潜力。