Pharmaceutical Sciences Faculty Publications
An Accurate Mass Tag Strategy for Quantitative and High Throughput Proteome Measurements
Document Type
Article
Publication Date
5-2002
Journal Title
Instrumentation Science & Technology
ISSN
1073-9149
Volume
30
Issue
2
First Page
211
Last Page
223
DOI
10.1081/CI-120003901
Abstract
We review a global strategy aimed at extending the breadth and throughput of proteomic measurements based on utilizing polypeptide "accurate mass tags" produced by global protein enzymatic digestion. The two-stage strategy described employs conventional mass spectrometric techniques to provide initial putative identifications of peptides based on searching genome databases using the partial sequence information gleaned from tandem mass spectrometric data. The second stage of the strategy utilizes advanced mass spectrometric instrumentation to "validate" those putative identifications initially made using conventional tandem mass spectrometric data. Specifically, the high mass accuracy provided by more advanced instrumentation is utilized and ultimately correlated with the conventional tandem mass spectrometric data (along with each of the peptides' liquid chromatographic elution time) to validate the putative identifications. The strategy described provides greater confidence in the assignment of protein identifications than possible with conventional tandem mass spectrometric data alone. The result is the generation of a database of accurate mass tags whose constituent peptides provide the basis for unambiguous identification of their cognate parent proteins and provide the basis for subsequent high throughput quantitative proteome measurements without the need for repeated tandem mass spectrometry.
Keywords
Proteome, proteomics, measurements, throughput, mass tag strategy
Recommended Citation
Conrads, Thomas P.; Issaq, Haleem J.; and Veenstra, Timothy D., "An Accurate Mass Tag Strategy for Quantitative and High Throughput Proteome Measurements" (2002). Pharmaceutical Sciences Faculty Publications. 517.
https://digitalcommons.cedarville.edu/pharmaceutical_sciences_publications/517