Combination of DNA‐directed immobilization and immuno‐PCR: very sensitive antigen detection by means of self‐assembled DNA–protein conjugates

An assay for very sensitive antigen detection is described which takes advantage of the self‐ assembly capabilities of semi‐synthetic conjugates of DNA and proteins. The general scheme of this assay is similar to a two‐sided (sandwich) enzyme‐linked immunoassay (ELISA); however, covalent single‐stra...

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Veröffentlicht in:Nucleic acids research 2003-08, Vol.31 (16), p.e90-e90
Hauptverfasser: Niemeyer, Christof M., Wacker, Ron, Adler, Michael
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Sprache:eng
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Zusammenfassung:An assay for very sensitive antigen detection is described which takes advantage of the self‐ assembly capabilities of semi‐synthetic conjugates of DNA and proteins. The general scheme of this assay is similar to a two‐sided (sandwich) enzyme‐linked immunoassay (ELISA); however, covalent single‐stranded DNA–streptavidin (STV) conjugates, capable of hybridizing to complementary surface‐bound DNA oligomers, are utilized for the effective immobilzation of either capture antibodies or antigens, rather than the chemi‐ or physisorption usually applied in ELISA. Immuno‐PCR (IPCR) is employed as a method for signal generation, utilizing oligomeric reagents obtained by self‐assembly of STV, biotinylated DNA and antibodies. In three different model systems, detecting human IgG, rabbit IgG or carcinoembryonic antigen, this combination allowed one to increase the sensitivity of the analogous ELISA ∼1000‐fold. For example,
ISSN:0305-1048
1362-4962
1362-4962
DOI:10.1093/nar/gng090