| Literature DB >> 30093420 |
Alexander B Saltzman1, Mei Leng1, Bhoomi Bhatt1, Purba Singh2, Doug W Chan2, Lacey Dobrolecki2,3, Hamssika Chandrasekaran4, Jong M Choi4, Antrix Jain4, Sung Y Jung1,4, Michael T Lewis2,5,3,6, Matthew J Ellis2,5,6, Anna Malovannaya7,6,4,5.
Abstract
In quantitative mass spectrometry, the method by which peptides are grouped into proteins can have dramatic effects on downstream analyses. Here we describe gpGrouper, an inference and quantitation algorithm that offers an alternative method for assignment of protein groups by gene locus and improves pseudo-absolute iBAQ quantitation by weighted distribution of shared peptide areas. We experimentally show that distributing shared peptide quantities based on unique peptide peak ratios improves quantitation accuracy compared with conventional winner-take-all scenarios. Furthermore, gpGrouper seamlessly handles two-species samples such as patient-derived xenografts (PDXs) without ignoring the host species or species-shared peptides. This is a critical capability for proper evaluation of proteomics data from PDX samples, where stromal infiltration varies across individual tumors. Finally, gpGrouper calculates peptide peak area (MS1) based expression estimates from multiplexed isobaric data, producing iBAQ results that are directly comparable across label-free, isotopic, and isobaric proteomics approaches.Entities:
Keywords: Bioinformatics software; Cancer Biology; Label-free quantification; Mass Spectrometry; Mouse models; Quantification; iTRAQ; patient derived xenograft; protein inference; shared peptides
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Year: 2018 PMID: 30093420 PMCID: PMC6210220 DOI: 10.1074/mcp.TIR118.000850
Source DB: PubMed Journal: Mol Cell Proteomics ISSN: 1535-9476 Impact factor: 5.911