A fluorescent assay for Clostridium Perfringens phospholipase C is described using l-palmitoyl-2-[6(pyren-l-yl)hexanoyl]-snglycero-3-phospho-N-(trinitrophenyl)aminoethanol (PPHTE) as the substrate. This method is based on the decrease of the quenching of pyrene monomer fluorescence when phospholipas
An electrochemical immunoassay for Clostridium perfringens phosholipase C
✍ Scribed by Marco Cardosi; Stephen Birch; Jane Talbot; Anthony Phillips
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 790 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1040-0397
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✦ Synopsis
Abstract
A sensitive two‐site, enzyme‐linked immunoassay utilizing electrochemical detection has been developed for Clostridium perfringens phospholipase C (α toxin). Alkaline phosphatase conjugated to a mouse monoclonal antibody is used as the enzyme label. The enzyme activity is measured using 1‐naphthyl phosphate as the enzyme substrate. The enzyme‐generated naphthol is detected amperometrically in a thin‐layer cell at a glassy carbon electrode after chromatography on a 50 mm C8 reverse phase column. Two assay formats are described, based on either microtiter plates or polydispersed polymeric microbeads. The limits of detection of the two assay formats were 67.1 and 13.0 ng/mL, respectively, with a total assay time of less than one hour. The performance characteristics of three possible substrates for the alkaline phosphatase catalyzed reaction are also described.
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