Toward Systeme International d'Unite-traceable protein quantification: From amino acids to proteins

被引:74
作者
Burkitt, William I. [1 ]
Pritchard, Caroline [1 ]
Arsene, Cristian [2 ]
Henrion, Andre [2 ]
Bunk, David [3 ]
O'Connor, Gavin [1 ]
机构
[1] LGC, Dept Bioorgan Mass Spectrometry, Teddington TW11 0LY, Middx, England
[2] Phys Tech Bundesanstalt, D-38116 Braunschweig, Germany
[3] Natl Inst Stand & Technol, Gaithersburg, MD 20899 USA
关键词
absolute protein quantification; SI-traceable; isotope dilution mass spectrometry; mass spectrometry and proteomics;
D O I
10.1016/j.ab.2008.02.010
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Here we present a demonstration of the proof of principle that absolute concentration of a protein within a mixture of other proteins can be measured with SI traceability. The method used was based on tryptic digestion of a protein followed by quantification using double exact matching isotope dilution mass spectrometry (IDMS) of the peptides released. To provide full SI traceability to measurements of protein concentration we demonstrated a method of SI traceable peptide quantification in which the peptide standards used were quantified by an amino acid analysis method that incorporated double exact matching IDMS and amino acid standards of known purity. The concentration of the protein was therefore determined based upon the concentration of tryptic peptides, which in turn had been quantified based upon amino acid standards. This allowed fully SI-traceable measurements of protein concentration to be made. Important caveats in the implementation of this approach are also discussed and examples of how these can have detrimental effects on the measurements are shown. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:242 / 251
页数:10
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