Body fluid identification by mass spectrometry

被引:72
作者
Yang, Heyi [1 ]
Zhou, Bo [1 ]
Deng, Haiteng [2 ]
Prinz, Mechthild [1 ]
Siegel, Donald [1 ]
机构
[1] New York City Off Chief Med Examiner, New York, NY 10016 USA
[2] Tsinghua Univ, Sch Life Sci, Beijing 100084, Peoples R China
关键词
Body fluid identification; Mass spectrometry; Protein markers; MALDI-TOF MS; PROTEOMIC ANALYSIS; FORENSIC IDENTIFICATION; SEMENOGELIN-I; RNA; EXPRESSION; PROTEINS; BLOOD; PRESERVATION; DEGRADATION;
D O I
10.1007/s00414-013-0848-1
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
Standard methods for body fluid identification typically rely on detection of the functional proteins specific to or enriched in them, such as hemoglobin in blood, alkaline phosphatase and PSA in semen, or alpha-amylase in saliva. While these markers can be relatively specific, the multiple methods used to identify them frequently rely on nonspecific chemical, enzymatic, or antibody reactions that usually require the structural integrity of the markers and are not confirmatory because other proteins or substances can also give positive test results. Recent advances in proteomics and mass spectrometry offer the ability to simultaneously detect multiple body fluid protein markers in a single, confirmatory test. Here, multiple markers for blood, saliva, and semen are identified by matrix-assisted laser desorption/ionization (MALDI) mass spectrometry (MS). Data demonstrate the ability to detect these body fluids at nanoliter to subnanoliter levels and to distinguish mixtures. Protein stability of mock samples assayed after 16 months showed no diminution of signal. Because multiple peptides from multiple protein markers are detected and effectively sequenced by MALDI MS/MS, the assay is confirmatory. As mass spectrometry detects whatever peptides are present in a sample, no a priori knowledge of an unknown stain is necessary to perform the test.
引用
收藏
页码:1065 / 1077
页数:13
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