Homogeneous antibody-based proximity extension assays provide sensitive and specific detection of low-abundant proteins in human blood

• Published in: Nucleic acids research 2011-08, Vol.39 (15), p.e102-e102
• Main Authors: Lundberg, Martin, Eriksson, Anna, Tran, Bonnie, Assarsson, Erika, Fredriksson, Simon
• Format: Article
• Language: English
• Subjects: Antibodies; Blood Proteins - analysis; Blood Proteins - immunology; Exonucleases; Humans; Immunoassay - methods; Methods Online; Oligonucleotide Probes; Polymerase Chain Reaction; Water - chemistry
• ISSN: 0305-1048; 1362-4962
• DOI: 10.1093/nar/gkr424

Convenient and well-performing protein detection methods for a wide range of targets are in great demand for biomedical research and future diagnostics. Assays without the need for washing steps while still unaffected when analyzing complex biological samples are difficult to develop. Herein, we report a well-characterized nucleic acid proximity-based assay using antibodies, called Proximity Extension Assay (PEA), showing good performance in plasma samples. Target-specific antibody pairs are linked to DNA strands that upon simultaneous binding to the target analyte create a real-time PCR amplicon in a proximity-dependent manner enabled by the action of a DNA polymerase. 3'Exonuclease-capable polymerases were found to be clearly superior in sensitivity over non-3'exonuclease ones. A PEA was set up for IL-8 and GDNF in a user-friendly, homogenous assay displaying femtomolar detection sensitivity, good recovery in human plasma, high specificity and up to 5-log dynamic range in 1 μL samples. Furthermore, we have illustrated the use of a macro-molecular crowding matrix in combination with this homogeneous assay to drive target binding for low-affinity antibodies, thereby improving the sensitivity and increasing affinity reagent availability by lowering assay development dependency on high-affinity antibodies. Assay performance was also confirmed for a multiplex version of PEA.