Targeted Quantitation of Proteins by Mass Spectrometry

被引:245
作者
Liebler, Daniel C.
Zimmerman, Lisa J.
机构
[1] Vanderbilt Univ, Sch Med, Vanderbilt Ingram Canc Ctr, Dept Biochem, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Vanderbilt Ingram Canc Ctr, Jim Ayers Inst Precanc Detect & Diag, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
SHOTGUN PROTEOMICS; ELECTROPHORETIC TRANSFER; PROTEOTYPIC PEPTIDES; POLYACRYLAMIDE GELS; SIGNALING NETWORKS; TRIPLE QUADRUPOLE; PLASMA-PROTEINS; HIGH-RESOLUTION; CELL-CULTURE; ION-TRAP;
D O I
10.1021/bi400110b
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Quantitative measurement of proteins is one of the most fundamental analytical tasks in a biochemistry laboratory, but widely used immunochemical methods often have limited specificity and high measurement variation. In this review, we discuss applications of multiple-reaction monitoring (MRM) mass spectrometry, which allows sensitive, precise quantitative analyses of peptides and the proteins from which they are derived. Systematic development of MRM assays is permitted by databases of peptide mass spectra and sequences, software tools for analysis design and data analysis and rapid evolution of tandem mass spectrometer technology. Key advantages of MRM assays are the ability to target specific peptide sequences, including variants and modified forms, and the capacity for multiplexing that allows analysis of dozens to hundreds of peptides. Different quantitative standardization methods provide options that balance precision, sensitivity, and assay cost. Targeted protein quantitation by MRM and related mass spectrometry methods can advance biochemistry by transforming approaches to protein measurement.
引用
收藏
页码:3797 / 3806
页数:10
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