Carol-Visser Jeroen, van der Schans Marcel, Fidder Alex, Hulst Albert G, van Baar Ben L M, Irth Hubertus, Noort Daan
Department of Analytical Chemistry and Applied Spectroscopy, Faculty of Sciences, Vrije Universiteit, De Boelelaan 1083, 1081 HV Amsterdam, The Netherlands.
J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Jul 1;870(1):91-7. doi: 10.1016/j.jchromb.2008.06.008. Epub 2008 Jun 11.
Rapid monitoring and retrospective verification are key issues in protection against and non-proliferation of chemical warfare agents (CWA). Such monitoring and verification are adequately accomplished by the analysis of persistent protein adducts of these agents. Liquid chromatography-mass spectrometry (LC-MS) is the tool of choice in the analysis of such protein adducts, but the overall experimental procedure is quite elaborate. Therefore, an automated on-line pepsin digestion-LC-MS configuration has been developed for the rapid determination of CWA protein adducts. The utility of this configuration is demonstrated by the analysis of specific adducts of sarin and sulfur mustard to human butyryl cholinesterase and human serum albumin, respectively.
快速监测和追溯性核查是防范化学战剂(CWA)及其不扩散的关键问题。通过分析这些战剂的持久性蛋白质加合物可充分实现此类监测和核查。液相色谱 - 质谱联用(LC-MS)是分析此类蛋白质加合物的首选工具,但整个实验过程相当复杂。因此,已开发出一种自动化在线胃蛋白酶消化 - LC-MS配置,用于快速测定CWA蛋白质加合物。通过分别分析沙林和硫芥与人丁酰胆碱酯酶和人血清白蛋白的特定加合物,证明了该配置的实用性。