Aptamer-Based Multiplexed Proteomic Technology for Biomarker Discovery

Larry Gold(University of Colorado Boulder), Deborah Ayers(SomaLogic (United States)), Jennifer Bertino(SomaLogic (United States)), C. Bock(SomaLogic (United States)), Ashley Bock(SomaLogic (United States)), Edward N. Brody(SomaLogic (United States)), Jeff Carter(SomaLogic (United States)), Andrew B Dalby(SomaLogic (United States)), Bruce E. Eaton(University of Colorado Boulder), Tim Fitzwater(SomaLogic (United States)), Dylan Flather(SomaLogic (United States)), Ashley Forbes(SomaLogic (United States)), Trudi Foreman(SomaLogic (United States)), Cate Fowler(SomaLogic (United States)), Bharat Gawande(SomaLogic (United States)), Meredith Goss(SomaLogic (United States)), Magda Gunn(SomaLogic (United States)), Shashi Kumar Gupta(SomaLogic (United States)), Dennis Halladay(SomaLogic (United States)), Jim Heil(SomaLogic (United States)), Joe Heilig(SomaLogic (United States)), Brian J. Hicke(SomaLogic (United States)), Gregory M. Husar(SomaLogic (United States)), Nebojša Janjić(SomaLogic (United States)), Thale C. Jarvis(SomaLogic (United States)), Susan Jennings(SomaLogic (United States)), Evaldas Katilius(SomaLogic (United States)), Tracy R. Keeney(SomaLogic (United States)), Nancy Kim(SomaLogic (United States)), Tad H. Koch(University of Colorado Boulder), Stephan Kräemer(SomaLogic (United States)), Luke Kroiss(SomaLogic (United States)), Ngan Le(SomaLogic (United States)), Daniel M. Levine(The Rogosin Institute), Wes Lindsey(SomaLogic (United States)), Bridget Lollo(SomaLogic (United States)), Wes Mayfield(SomaLogic (United States)), Mike Mehan(SomaLogic (United States)), Robert Mehler(SomaLogic (United States)), S. Kim Nelson(SomaLogic (United States)), Michele Nelson(SomaLogic (United States)), Dan Nieuwlandt(SomaLogic (United States)), Malti Nikrad(SomaLogic (United States)), Urs A. Ochsner(SomaLogic (United States)), Rachel Ostroff(SomaLogic (United States)), Matt Otis(SomaLogic (United States)), Thomas S. Parker(The Rogosin Institute), Steve Pietrasiewicz(SomaLogic (United States)), Daniel I. Resnicow(SomaLogic (United States)), John C. Rohloff(SomaLogic (United States)), Glenn M. Sanders(SomaLogic (United States)), Sarah Sattin(SomaLogic (United States)), Daniel J. Schneider(SomaLogic (United States)), Britta Swebilius Singer(SomaLogic (United States)), Martin Stanton(SomaLogic (United States)), Alana Sterkel(SomaLogic (United States)), Alexandre F.R. Stewart(SomaLogic (United States)), Suzanne Stratford(SomaLogic (United States)), Jonathan D. Vaught(SomaLogic (United States)), Mike Vrkljan(SomaLogic (United States)), Jeffrey J. Walker(SomaLogic (United States)), Mike Watrobka(SomaLogic (United States)), Sheela Waugh(SomaLogic (United States)), Allison Weiss(SomaLogic (United States)), Sheri K. Wilcox(SomaLogic (United States)), Alexey Wolfson(SomaLogic (United States)), Steven K. Wolk(SomaLogic (United States)), Chi Zhang(SomaLogic (United States)), Dom Zichi(SomaLogic (United States))
PLoS ONE
December 7, 2010
Cited by 1,733Open Access
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Abstract

BACKGROUND: The interrogation of proteomes ("proteomics") in a highly multiplexed and efficient manner remains a coveted and challenging goal in biology and medicine. METHODOLOGY/PRINCIPAL FINDINGS: We present a new aptamer-based proteomic technology for biomarker discovery capable of simultaneously measuring thousands of proteins from small sample volumes (15 µL of serum or plasma). Our current assay measures 813 proteins with low limits of detection (1 pM median), 7 logs of overall dynamic range (~100 fM-1 µM), and 5% median coefficient of variation. This technology is enabled by a new generation of aptamers that contain chemically modified nucleotides, which greatly expand the physicochemical diversity of the large randomized nucleic acid libraries from which the aptamers are selected. Proteins in complex matrices such as plasma are measured with a process that transforms a signature of protein concentrations into a corresponding signature of DNA aptamer concentrations, which is quantified on a DNA microarray. Our assay takes advantage of the dual nature of aptamers as both folded protein-binding entities with defined shapes and unique nucleotide sequences recognizable by specific hybridization probes. To demonstrate the utility of our proteomics biomarker discovery technology, we applied it to a clinical study of chronic kidney disease (CKD). We identified two well known CKD biomarkers as well as an additional 58 potential CKD biomarkers. These results demonstrate the potential utility of our technology to rapidly discover unique protein signatures characteristic of various disease states. CONCLUSIONS/SIGNIFICANCE: We describe a versatile and powerful tool that allows large-scale comparison of proteome profiles among discrete populations. This unbiased and highly multiplexed search engine will enable the discovery of novel biomarkers in a manner that is unencumbered by our incomplete knowledge of biology, thereby helping to advance the next generation of evidence-based medicine.


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