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Two-color, rolling-circle amplification on antibody microarrays for sensitive, multiplexed serum-protein measurements

Heping Zhou1, Kerri Bouwman1, Mark Schotanus1, Cornelius Verweij2, Jorge A Marrero3, Deborah Dillon4, Jose Costa4, Paul Lizardi4 and Brian B Haab1*

Author affiliations

1 The Van Andel Research Institute, 333 Bostwick, Grand Rapids, MI 49503, USA

2 The University of Amsterdam, Department of Molecular and Cell Biology, 1081 BT Amsterdam, The Netherlands

3 The University of Michigan Medical School, 1500 East Medical Center Drive, Ann Arbor, MI 48109, USA

4 Yale University School of Medicine, Department of Pathology, 310 Cedar Street, New Haven, CT 06510, USA

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Citation and License

Genome Biology 2004, 5:R28  doi:

Published: 30 March 2004

Abstract

The ability to conveniently and rapidly profile a diverse set of proteins has valuable applications. In a step toward further enabling such a capability, we developed the use of rolling-circle amplification (RCA) to measure the relative levels of proteins from two serum samples, labeled with biotin and digoxigenin, respectively, that have been captured on antibody microarrays. Two-color RCA produced fluorescence up to 30-fold higher than direct-labeling and indirect-detection methods using antibody microarrays prepared on both polyacrylamide-based hydrogels and nitrocellulose. Replicate RCA measurements of multiple proteins from sets of 24 serum samples were highly reproducible and accurate. In addition, RCA enabled reproducible measurements of distinct expression profiles from lower-abundance proteins that were not measurable using the other detection methods. Two-color RCA on antibody microarrays should allow the convenient acquisition of expression profiles from a great diversity of proteins for a variety of applications.