One-step immunoassay for measuring protein concentrations in plasma, based on precipitate-enhanced ellipsometry

Standard enzyme immunoassays (EIAs) require washing steps to remove excess enzyme–antibody complexes. Such washing is laborious, lengthens assay time, and increases assay scatter. Recently, so-called precipitate-enhanced immunoassays (PEIAs) were introduced. Instead of color formation due to enzymat...

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Published inAnalytical biochemistry Vol. 326; no. 2; pp. 257 - 261
Main Authors Speijer, Han, Laterveer-Vreeswijk, Ria H, Glatz, Jan F.C, Nieuwenhuizen, Willem, Hermens, Wim T
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 15.03.2004
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Summary:Standard enzyme immunoassays (EIAs) require washing steps to remove excess enzyme–antibody complexes. Such washing is laborious, lengthens assay time, and increases assay scatter. Recently, so-called precipitate-enhanced immunoassays (PEIAs) were introduced. Instead of color formation due to enzymatic conversion of a chromogenic substrate, this technique measures the rate of precipitate formation due to conversion of a substrate with a precipitating product. Such precipitation can be measured in the presence of active enzyme–antibody complexes in the buffer and no washing is required. In the present study this technique was used in a one-step PEIA, without washing steps, for the measurement of plasma concentrations of fatty-acid-binding protein. Horseradish peroxidase was used as tagging enzyme and diaminobenzidine as precipitating substrate. Precipitate formation was measured by ellipsometry. Assay time of the one-step PEIA was much shorter than that for an existing standard EIA. Test results can be obtained within minutes, depending on the sensitivity required. Assay precision of the one-step PEIA was better than that of the standard EIA. In the one-step assay, loss of surface-bound conjugate due to washing is prevented, which could explain part of the improved sensitivity compared to that of the two-step PEIA. More importantly, the presence of substrate-converting enzyme–antibody complexes in the buffer caused a large enhancement of precipitation.
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ISSN:0003-2697
1096-0309
DOI:10.1016/j.ab.2003.12.008