Adenosine reagent-free detection by co-immobilization of adenosine deaminase and phenol red on an optical biostrip

Adenosine detection in human serum is important because this ribonucleoside has established clinical applications, modulating many physiological processes. Furthermore, a simple and cheap detection method is useful in adenosine production processes. Adenosine can be determined enzymatically using ei...

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Published inBiotechnology journal Vol. 10; no. 1; p. 136
Main Authors Bartzoka, Foteini, Venetsanou, Katerina, Clonis, Yannis
Format Journal Article
LanguageEnglish
Published Germany 01.01.2015
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Abstract Adenosine detection in human serum is important because this ribonucleoside has established clinical applications, modulating many physiological processes. Furthermore, a simple and cheap detection method is useful in adenosine production processes. Adenosine can be determined enzymatically using either S-adenosyl-homocysteine hydrolase and (3) [H]-adenosine, or adenosine kinase combined with GTP and luciferase, or an amperometric biosensor carrying adenosine deaminase (ADA), purine nucleoside phosphorylase, and xanthine oxidase. We developed a simple and cheap method relying on a transparent biostrip bearing ADA and the indicator phenol red (PR), co-immobilized to polyacrylamide, itself chemically adhered to a derivatized glass strip. The ADA-catalyzed conversion of adenosine to inosine and ammonia leads to a local pH alteration, changing the absorbance maximum of PR (from 425 to 567 nm), which is measured optically. The biostrip shows an analytical range 0.05-1.5 mM adenosine and is reusable when stored at 4 °C. When the biostrip was tested with serum, spiked with adenosine (70 and 100 μM), and filtered for protein and adenosine phosphates depletion, it showed good adenosine recovery. In summary, we show the proof-of-concept that adenosine can be determined reagent-free, at moderate sensitivity on an easy to construct, cheap, and reusable biostrip, based on commercially available molecular entities.
AbstractList Adenosine detection in human serum is important because this ribonucleoside has established clinical applications, modulating many physiological processes. Furthermore, a simple and cheap detection method is useful in adenosine production processes. Adenosine can be determined enzymatically using either S-adenosyl-homocysteine hydrolase and (3) [H]-adenosine, or adenosine kinase combined with GTP and luciferase, or an amperometric biosensor carrying adenosine deaminase (ADA), purine nucleoside phosphorylase, and xanthine oxidase. We developed a simple and cheap method relying on a transparent biostrip bearing ADA and the indicator phenol red (PR), co-immobilized to polyacrylamide, itself chemically adhered to a derivatized glass strip. The ADA-catalyzed conversion of adenosine to inosine and ammonia leads to a local pH alteration, changing the absorbance maximum of PR (from 425 to 567 nm), which is measured optically. The biostrip shows an analytical range 0.05-1.5 mM adenosine and is reusable when stored at 4 °C. When the biostrip was tested with serum, spiked with adenosine (70 and 100 μM), and filtered for protein and adenosine phosphates depletion, it showed good adenosine recovery. In summary, we show the proof-of-concept that adenosine can be determined reagent-free, at moderate sensitivity on an easy to construct, cheap, and reusable biostrip, based on commercially available molecular entities.
Author Clonis, Yannis
Bartzoka, Foteini
Venetsanou, Katerina
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Issue 1
Keywords Reagent-free
Adenosine deaminase
Adenosine detection
Biosensor
Phenol red
Language English
License Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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Snippet Adenosine detection in human serum is important because this ribonucleoside has established clinical applications, modulating many physiological processes....
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StartPage 136
SubjectTerms Adenosine - analysis
Adenosine - metabolism
Adenosine Deaminase - chemistry
Adenosine Deaminase - metabolism
Biosensing Techniques - methods
Enzyme Stability
Enzymes, Immobilized - chemistry
Enzymes, Immobilized - metabolism
Limit of Detection
Phenolsulfonphthalein - chemistry
Phenolsulfonphthalein - metabolism
Title Adenosine reagent-free detection by co-immobilization of adenosine deaminase and phenol red on an optical biostrip
URI https://www.ncbi.nlm.nih.gov/pubmed/25293641
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