Analysis of iTRAQ data using Mascot and Peaks quantification algorithms
Author(s) -
Carla M. R. Lacerda,
Lei Xin,
Iain Rogers,
Kenneth F. Reardon
Publication year - 2008
Publication title -
briefings in functional genomics and proteomics
Language(s) - English
Resource type - Journals
eISSN - 1477-4062
pISSN - 1473-9550
DOI - 10.1093/bfgp/eln017
Subject(s) - mascot , mass spectrometry , software , proteomics , quantitative proteomics , field (mathematics) , computer science , peptide , biology , computational biology , algorithm , biological system , chromatography , chemistry , biochemistry , mathematics , political science , pure mathematics , law , gene , programming language
The field of proteomics has been developing rapidly toward quantification of proteins. Despite the variety of experimental techniques available for peptide and protein labelling, there are few commercially available analytical tools with the ability to interpret data from any mass spectrometer. In this study, we compare two software packages, Mascot and Peaks, for the analysis of iTRAQ data from ESI-Q/TOF mass spectrometry. In the case of a six-protein mixture combined in a known proportion, the output of the Peaks algorithm deviated from the correct result by 14% on average, while the error of the Mascot quantification was nearly 200%. When the software were used to analyse iTRAQ data from a complex protein sample, the quantification results agreed within 20% for only 26% of the quantified proteins, showing significant differences in the two quantification algorithms. This comparison and analysis revealed major intricacies in peptide and protein quantification that must be taken into consideration for software development.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom