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Identification of short terminal motifs enriched by antibodies using peptide mass fingerprinting
Author(s) -
Hannes Planatscher,
F. T. Weiss,
David Eisen,
Bart H. J. van den Berg,
Andreas Zell,
Thomas Joos,
Oliver Poetz
Publication year - 2014
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btu009
Subject(s) - epitope , computational biology , proteome , peptide mass fingerprinting , proteomics , peptide , bottom up proteomics , mass spectrometry , peptide library , antibody , chemistry , monoclonal antibody , context (archaeology) , peptide sequence , epitope mapping , tandem mass spectrometry , biology , biochemistry , protein mass spectrometry , chromatography , genetics , gene , paleontology
Mass spectrometry-based protein profiling has become a key technology in biomedical research and biomarker discovery. Sample preparation strategies that reduce the complexity of tryptic digests by immunoaffinity substantially increase throughput and sensitivity in proteomic mass spectrometry. The scarce availability of peptide-specific capture antibodies limits these approaches. Recently antibodies directed against short terminal motifs were found to enrich subsets of peptides with identical terminal sequences. This approach holds the promise of a significant gain in efficiency. TXP (Triple X Proteomics) and context-independent motif specific/global proteome survey binders are variants of this concept. Principally the binding motifs of such antibodies have to be elucidated after generating these antibodies. This entails a substantial effort in the lab, as it requires synthetic peptide libraries and numerous mass spectrometry experiments.

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