Heart disease, clinical proteomics and mass spectrometry

被引:52
作者
Stanley, BA
Gundry, RL
Cotter, RJ
Van Eyk, JE
机构
[1] Johns Hopkins Univ, Dept Pharmacol, Baltimore, MD 21224 USA
[2] Johns Hopkins Univ, Dept Med, Baltimore, MD USA
[3] Queens Univ, Dept Physiol, Kingston, ON K7L 3N6, Canada
关键词
D O I
10.1155/2004/965261
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Heart disease is the leading cause of mortality and morbidity in the world. As such, biomarkers are needed for the diagnosis, prognosis, therapeutic monitoring and risk stratification of acute injury (acute myocardial infarction (AMI)) and chronic disease (heart failure). The procedure for biomarker development involves the discovery, validation, and translation into clinical practice of a panel of candidate proteins to monitor risk of heart disease. Two types of biomarkers are possible; heart-specific and cardiovascular pulmonary system monitoring markers. Here we review the use of MS in the process of cardiac biomarker discovery and validation by proteomic analysis of cardiac myocytes/ tissue or serum/plasma. An example of the use of MS in biomarker discovery is given in which the albumin binding protein sub-proteome was examined using MALDI-TOF MS/MS. Additionally, an example of MS in protein validation is given using affinity surface enhanced laser desorption ionization (SELDI) to monitor the disease-induced post-translational modification and the ternary status of myoctye-originating protein, cardiac troponin I in serum.
引用
收藏
页码:167 / 178
页数:12
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