Kinder- und Jugendklinik, Universitätsklinikum Erlangen, Erlangen, Germany.
J Chromatogr B Analyt Technol Biomed Life Sci. 2012 Feb 1;883-884:59-67. doi: 10.1016/j.jchromb.2011.09.030. Epub 2011 Sep 22.
The LC-triple quadrupole mass spectrometer (LC-MS/MS) is an increasingly common tool in the clinical laboratory. Established applications include routine assays for detecting inborn errors of metabolism, and for monitoring therapeutic drugs and steroids. Peptides and proteins in biological matrices have traditionally been quantified by immunological methods such as RIA or ELISA. These methods have the drawback of being insufficiently selective, often not allowing differentiation between the peptide and its derivatives or degradation fragments. The improved robustness and sensitivity of LC-MS-based techniques provide reliable alternatives for peptide quantification. Mass spectrometry does not require specific antibody reagents and is a powerful tool for the study of posttranslational modifications (PTM). In addition, several studies have demonstrated the utility of selected reaction monitoring (SRM) assays using stable-isotope-labelled (tryptic) peptides for quantifying proteins in human serum. Peptide-based MS/MS is a relatively new development in the measurement of clinically significant proteins, offering cost effectiveness, high throughput, multiplexed analysis and quantification, with the potential for combining the measurement of small molecules, peptides and proteins on a single technology platform. Quantitative analysis of proteins and peptides by LC-MS/MS is becoming a practical technique for clinical laboratories. To move from the laboratories of highly skilled analysts to routine clinical diagnostic laboratories requires that a number of technical hurdles be overcome in regard to sensitivity, imprecision, accuracy and the sample handling necessary for clinical use.
LC-三重四极杆质谱仪(LC-MS/MS)是临床实验室中越来越常用的工具。已建立的应用包括用于检测先天性代谢错误的常规检测,以及用于监测治疗药物和类固醇的常规检测。生物基质中的肽和蛋白质传统上通过免疫测定法(如 RIA 或 ELISA)进行定量。这些方法的缺点是选择性不足,通常不允许区分肽与其衍生物或降解片段。基于 LC-MS 的技术的改进的稳健性和灵敏度为肽定量提供了可靠的替代方法。质谱法不需要特定的抗体试剂,是研究翻译后修饰(PTM)的有力工具。此外,几项研究已经证明了使用稳定同位素标记(胰蛋白酶)肽的选择反应监测(SRM)测定在定量人血清中的蛋白质方面的实用性。基于肽的 MS/MS 是测量临床上有意义的蛋白质的相对较新的发展,具有成本效益高、高通量、多重分析和定量的优点,并且有可能将小分子、肽和蛋白质的测量结合在单个技术平台上。LC-MS/MS 对蛋白质和肽的定量分析正在成为临床实验室的实用技术。要从高度熟练的分析师实验室转移到常规临床诊断实验室,需要克服许多技术障碍,包括灵敏度、不精密度、准确性以及临床使用所需的样品处理。