Microarray-based kinetic colorimetric detection for quantitative multiplex protein phosphorylation analysis

Commonly used colorimetric detection applied to protein microarrays with enzymatic signal amplification leads to non-linear signal production upon increase in analyte concentration, thereby considerably limiting the range and accuracy of quantitative readout interpretation. To extend the detection r...

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Bibliographic Details
Main Authors: Holenya, Pavlo (Author) , Kitanovic, Igor (Author) , Heigwer, Florian (Author) , Wölfl, Stefan (Author)
Format: Article (Journal)
Language:English
Published: 08 March 2011
In: Proteomics
Year: 2011, Volume: 11, Issue: 10, Pages: 2129-2133
ISSN:1615-9861
DOI:10.1002/pmic.201000690
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/pmic.201000690
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/pmic.201000690
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Author Notes:Pavlo Holenya, Igor Kitanovic, Florian Heigwer, and Stefan Wölfl
Description
Summary:Commonly used colorimetric detection applied to protein microarrays with enzymatic signal amplification leads to non-linear signal production upon increase in analyte concentration, thereby considerably limiting the range and accuracy of quantitative readout interpretation. To extend the detection range, we developed a kinetic colorimetric detection protocol for the analysis of ELISA microarrays designed to measure multiple phosphorylated proteins using the platforms ArrayTube™ and ArrayStrip™. With our novel quantification approach, microarrays were calibrated over a broad concentration range spanning four orders of magnitude of analyte concentration with picomolar threshold. We used this design for the simultaneous quantitative measurement of 15 phosphorylated proteins on a single chip.
Item Description:Gesehen am 29.06.2022
Physical Description:Online Resource
ISSN:1615-9861
DOI:10.1002/pmic.201000690