4.5 Article

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

Journal

GENOME BIOLOGY
Volume 5, Issue 4, Pages -

Publisher

BMC
DOI: 10.1186/gb-2004-5-4-r28

Keywords

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Funding

  1. NATIONAL CANCER INSTITUTE [U01CA084986, R33CA081671] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [P30DK034989] Funding Source: NIH RePORTER
  3. NCI NIH HHS [CA81671, UO1 CA084986] Funding Source: Medline
  4. NIDDK NIH HHS [P30 DK 34989] Funding Source: Medline

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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.

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