Martin Lundberg,
Stine Buch Thorsen,
Erika Assarsson, Andrea Villablanca,
Bonnie Tran,
Nick Gee,
Mick Knowles,
Birgitte Sander Nielsen,
Eduardo González Couto,
Roberto Martin, [......],
Christian Fermer,
Jörg Schlingemann,
Ib Jarle Christensen,
Hans-Jorgen Nielsen,
Björn Ekström,
Claes Andersson,
Mats Gustafsson,
Nils Brunner,
Jan Stenvang,
Simon Fredriksson
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ABSTRACT: A high throughput protein biomarker discovery tool has been developed based on multiplexed proximity ligation assays in a homogeneous format in the sense of no washing steps. The platform consists of four 24-plex panels profiling 74 putative biomarkers with sub-pm sensitivity each consuming only 1 μl of human plasma sample. The system uses either matched monoclonal antibody pairs or the more readily available single batches of affinity purified polyclonal antibodies to generate the target specific reagents by covalently linking with unique nucleic acid sequences. These paired sequences are united by DNA ligation upon simultaneous target binding forming a PCR amplicon. Multiplex proximity ligation assays thereby converts multiple target analytes into real-time PCR amplicons that are individually quantified using microfluidic high capacity qPCR in nano liter volumes. The assay shows excellent specificity, even in multiplex, by its dual recognition feature, its proximity requirement, and most importantly by using unique sequence specific reporter fragments on both antibody-based probes. To illustrate the potential of this protein detection technology, a pilot biomarker research project was performed using biobanked plasma samples for the detection of colorectal cancer using a multivariate signature.
Molecular & Cellular Proteomics 01/2011; 10(4):M110.004978. · 7.40 Impact Factor
