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Targeted Quantitation of Proteins by Mass Spectrometry

[Image: see text] 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 moni...

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Autores principales: Liebler, Daniel C., Zimmerman, Lisa J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2013
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674507/
https://www.ncbi.nlm.nih.gov/pubmed/23517332
http://dx.doi.org/10.1021/bi400110b
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author Liebler, Daniel C.
Zimmerman, Lisa J.
author_facet Liebler, Daniel C.
Zimmerman, Lisa J.
author_sort Liebler, Daniel C.
collection PubMed
description [Image: see text] 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.
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spelling pubmed-36745072013-06-07 Targeted Quantitation of Proteins by Mass Spectrometry Liebler, Daniel C. Zimmerman, Lisa J. Biochemistry [Image: see text] 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. American Chemical Society 2013-03-21 2013-06-04 /pmc/articles/PMC3674507/ /pubmed/23517332 http://dx.doi.org/10.1021/bi400110b Text en Copyright © 2013 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Liebler, Daniel C.
Zimmerman, Lisa J.
Targeted Quantitation of Proteins by Mass Spectrometry
title Targeted Quantitation of Proteins by Mass Spectrometry
title_full Targeted Quantitation of Proteins by Mass Spectrometry
title_fullStr Targeted Quantitation of Proteins by Mass Spectrometry
title_full_unstemmed Targeted Quantitation of Proteins by Mass Spectrometry
title_short Targeted Quantitation of Proteins by Mass Spectrometry
title_sort targeted quantitation of proteins by mass spectrometry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674507/
https://www.ncbi.nlm.nih.gov/pubmed/23517332
http://dx.doi.org/10.1021/bi400110b
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