Sample preparation strategies for targeted proteomics via proteotypic peptides in human blood using liquid chromatography tandem mass spectrometry

被引:33
|
作者
Dittrich, Julia [1 ,2 ]
Becker, Susen [1 ,2 ]
Hecht, Max [1 ]
Ceglarek, Uta [1 ,2 ]
机构
[1] Univ Hosp Leipzig, Inst Lab Med Clin Chem & Mol Diagnost, D-04103 Leipzig, Germany
[2] Univ Leipzig, LIFE Leipzig Res Ctr Civilizat Dis, D-04109 Leipzig, Germany
关键词
Absolute quantification of proteins; Proteotypic peptides; Quantitative proteomics; Sample pretreatment; Tryptic digestion; INTENSITY FOCUSED ULTRASOUND; SOLUTION PROTEIN DIGESTION; AQUEOUS SOLVENT SYSTEMS; LOW-ABUNDANCE PROTEINS; APOLIPOPROTEIN-A-I; QUANTITATIVE PROTEOMICS; HUMAN PLASMA; ABSOLUTE QUANTIFICATION; ISOTOPE-DILUTION; ENZYMATIC DIGESTION;
D O I
10.1002/prca.201400121
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The simultaneous quantification of protein concentrations via proteotypic peptides in human blood by liquid chromatography coupled to quadrupole MS/MS is an important field of bioanalytical research with a high potential for routine diagnostic applications. This review summarizes currently available sample preparation procedures and trends for absolute protein quantification in blood using LC-MS/MS. It discusses approaches of transferring established qualitative protocols to a quantitative analysis regarding their reliability and reproducibility. Techniques used to enhance method sensitivity such as the depletion of high-abundant proteins or the immunoaffinity enrichment of proteins and peptides are described. Furthermore, workflows for (i) protein denaturation, (ii) disulfide bridge reduction and (iii) thiol alkylation as well as (iv) enzymatic digestion for absolute protein quantification are presented. The main focus is on the tryptic digestion as a bottleneck of protein quantification via proteotypic peptides. Conclusively, requirements for a high-throughput application are discussed.
引用
收藏
页码:5 / 16
页数:12
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