Fiber-optic biosensor with fluorescence detection based on immobilized alkaline phosphatase
β Scribed by Mary K. Freeman; Leonidas G. Bachas
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 704 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0956-5663
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β¦ Synopsis
A method for quantifying the concentration of an enzymatic substrate has been demonstrated that is based on competition between two substrates for the active site of an enzyme. This was accomplished by fling the concentration of a substrate whose reaction can be monitored optically, and observing the effect of the addition of a second substrate whose concentration was to be determined The model enzyme, alkaline phosphatase, was immobilized on a nylon mesh, which was placed in front of a bifurcated fiber-optic bundle. The concentration of 4methylumbelliferyl phosphate in the sample solution was fixed This substrate of alkaline phosphatase becomes a highly fluorescent molecule upon hydrolysis of the phosphate ester. The rate of fluorescence production as a result of this reaction was monitored. The addition of a second substrate caused a decrease in the rate of fluorescence production and, therefore, an apparent inhibition of the enzyme. This method was demonstrated for two different substrates of alkaline phosphatase.
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## Abstract A novel method for the determination of alkaline phosphatase (ALP) isoenzymes in individual fibroblast cells of mouse bone marrow was developed by combining capillary electrophoresis with an onβcapillary enzymeβcatalyzed reaction and electrochemical detection. In this method, a single a