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Detection of human asialo-α1-acid glycoprotein using a heterosandwich immunoassay in conjunction with the light addressable potentiometric sensor

  • Glycoconjugate Journal
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Abstract

Highly specific detection of human α1-acid glycoprotein (AGP) and asialo-α1-acid glycoprotein (asialo-AGP) was made possible by use of a sandwich immunoassay. The glycoproteins were sandwiched between biotinylated and fluoresceinated polyclonal rabbit anti-human AGP antibodies. Additionally, asialo-AGP could be distinctly detected, apart from AGP, via the formation of a heterosandwich immunoassay using biotinylated polyclonal rabbit antihuman AGP and the lectin, fluoresceinated ricin toxin. Streptavidin was added to the formed immunocomplexes and the immunocomplexes captured on a biotinylated nitrocellulose membrane. The signal generator, urease conjugate of an anti-fluorescein antibody, was then bound to the complex on membrane. The rate of pH change under microvolume conditions (0.6 µl) was monitored using a silicon chip-based, light addressable potentiometer sensor. Results indicated that AGP and asialo-AGP can be detected to the 2 pg level when two antibodies are used to form the immunocomplex. Asialo-AGP can be detected down to 250 pg when the heterosandwich immunoassay is used; this assay exhibited no response up to 10 ng for native AGP or asialofetuin. Both immunoassays can be used to quantify the level of AGP and asialo-AGP in solution. Although the assay presented is very specific for AGP, asialo-AGP and terminal galactose, it is readily adaptable for the detection of any glycoprotein and terminal carbohydrate (or branched structure) by use of a protein-specific antibody and various lectins.

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Dill, K., Bearden, D.W. Detection of human asialo-α1-acid glycoprotein using a heterosandwich immunoassay in conjunction with the light addressable potentiometric sensor. Glycoconjugate J 13, 637–641 (1996). https://doi.org/10.1007/BF00731452

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  • DOI: https://doi.org/10.1007/BF00731452

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