Proteome Center Rostock, Medical Faculty and Natural Science Faculty, University of Rostock, Schillingallee 69, Rostock, 18057, Germany.
Department of Obstetrics and Gynecology, Medical Faculty, University of Rostock, Clinic Südstadt, Rostock, 18059, Germany.
Rapid Commun Mass Spectrom. 2021 Jul 31;35(14):e9121. doi: 10.1002/rcm.9121.
To open up new ways for matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS)-based patient screening, blood serum is the most preferred specimen because of its richness in patho-physiological information and due to ease of collection. To overcome deleterious freeze/thaw cycles and to reduce high costs for shipping and storage, we sought to develop a procedure which enables MALDI-MS protein profiling of blood serum proteins without the need for serum freezing.
Blood sera from patients/donors were divided into portions which after pre-incubation were fast frozen. Thawed aliquots were deposited on filter paper discs and air-dried at room temperature. Intact serum proteins were eluted with acid-labile detergent-containing solutions and were desalted by employing a reversed-phase bead system. Purified protein solutions were screened by MALDI-MS using standardized instrument settings.
MALDI mass spectra from protein solutions which were eluted from filter paper discs and desalted showed on average 25 strong ion signals (mass range m/z 6000 to 10,000) from intact serum proteins (apolipoproteins, complement proteins, transthyretin and hemoglobin) and from proteolytic processing products. Semi-quantitative analysis of three ion pairs: m/z 6433 and 6631, m/z 8205 and 8916, as well as m/z 9275 and 9422, indicated that the mass spectra from either pre-incubated fast-frozen serum or pre-incubated dried serum spot eluted serum contained the same information on protein composition.
A workflow that avoids the conventional cold-chain and yet enables the investigation of intact serum proteins and/or serum proteolysis products by MALDI-MS profiling was developed. The presented protocol tremendously broadens the clinical application of MALDI-MS and simultaneously allows a reduction in the costs for storage and shipping of serum samples. This will pave the way for clinical screening of patients also in areas with limited access to health care systems, and/or specialized laboratories.
为了开拓基质辅助激光解吸电离飞行时间质谱(MALDI-TOF-MS)基础上的患者筛选的新途径,由于富含病理生理信息且易于采集,血清是最优选的标本。为了克服有害的冻融循环并降低运输和储存的高成本,我们寻求开发一种不需要血清冷冻即可进行 MALDI-MS 血清蛋白谱分析的程序。
将患者/供体的血清分成几部分,预孵育后快速冷冻。解冻的等分试样被沉积在滤纸片上,并在室温下空气干燥。使用含有酸不稳定洗涤剂的溶液洗脱完整的血清蛋白,并通过反相珠系统进行脱盐。使用标准化仪器设置通过 MALDI-MS 筛选纯化的蛋白溶液。
从滤纸片洗脱并脱盐的蛋白溶液的 MALDI 质谱平均显示 25 个来自完整血清蛋白(载脂蛋白、补体蛋白、转甲状腺素蛋白和血红蛋白)和蛋白水解处理产物的强离子信号(分子量范围 m/z 6000 至 10000)。对三个离子对(m/z 6433 和 6631、m/z 8205 和 8916 以及 m/z 9275 和 9422)的半定量分析表明,来自预孵育快速冷冻血清或预孵育干燥血清斑点洗脱血清的质谱包含相同的蛋白质组成信息。
开发了一种避免传统冷链但仍能够通过 MALDI-MS 谱分析研究完整血清蛋白和/或血清蛋白水解产物的工作流程。所提出的方案极大地拓宽了 MALDI-MS 的临床应用,同时降低了血清样本储存和运输的成本。这将为在医疗保健系统有限或缺乏专门实验室的地区的患者临床筛查铺平道路。