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Development of a multiplex immunoassay for receptor signaling protein analysis
Author(s) -
Wiese Rick,
Harbison Stephen,
Hayes David
Publication year - 2012
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.26.1_supplement.577.2
Subject(s) - multiplex , immunoassay , phosphorylation , computational biology , peptide , biology , signal transduction , protein phosphorylation , antibody , microbiology and biotechnology , chemistry , bioinformatics , biochemistry , genetics , protein kinase a
Cellular signaling analysis is integral to a thorough understanding of living systems. Cellular analysis methods traditionally have involved the examination of single targets, but new techniques allow for multiplex analysis of proteins. MILLIPLEX® EpiQuant™ technology is an answer to multiplex limitations such as antibody cross‐reactivity and the inability to accurately quantify target protein levels. EpiQuant technology uses computational algorithms to identify unique peptide sequences in proteins. Antibodies generated against these sequences have pre‐defined target specificity. Total protein and protein phosphorylation measurements are made at the peptide level, using EpiQuant antibodies, following proteolytic fragmentation of samples. This process has a number of benefits including: a synthetic peptide can be used as a quantitative standard, cross‐reactivity with similar peptide sequences in other proteins can be predicted and avoided and multi‐site phosphorylated and total protein analysis of a single protein can be conducted in a single well. These attributes result in a superior methodology for cellular signaling multiplex analysis. We have utilized the EpiQuant technology to develop a multiplex assay consisting of 13 receptor signaling related protein targets, as well as, phosphorylation sites on these proteins, yielding a 27‐plex immunoassay. These total and phosphorylated protein targets include HER2, HER3, VEGFR1 and VEGFR2, among others. Here we demonstrate the use of this panel for the analysis of various stimulated tissue culture lysates.