2013Angewandte Chemie International EditionOpen access

Enzymatic Interconversion of Isomorphic Fluorescent Nucleosides: Adenosine Deaminase Transforms an Adenosine Analogue into an Inosine Analogue

Renatus W. Sinkeldam, Lisa S. McCoy, Dongwon Shin, Yitzhak Tor

Open full text 47 citations

Abstract

Adenosine deaminase (ADA), a major enzyme involved in purine metabolism, converts an isomorphic fluorescent analogue of adenosine (thA) into an isomorphic inosine analogue (thI), which possesses distinct spectral features, allowing one to monitor the enzyme-catalyzed reaction and its inhibition in real time. The utility of this sensitive fluorescence-monitored transformation for the high-throughput detection and analysis of ADA inhibitors is demonstrated.

Open-access reader

About this research paper

What this paper is about

Adenosine deaminase (ADA), a major enzyme involved in purine metabolism, converts an isomorphic fluorescent analogue of adenosine (thA) into an isomorphic inosine analogue (thI), which possesses distinct spectral features, allowing one to monitor the enzyme-catalyzed reaction and its inhibition in real time. The utility of this sensitive fluorescence-monitored transformation for the high-throughput detection and analysis of ADA inhibitors is demonstrated.

Why it matters

OpenAlex reports 47 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Adenosine deaminase (ADA), a major enzyme involved in purine metabolism, converts an isomorphic fluorescent analogue of adenosine (thA) into an isomorphic inosine analogue (thI), which possesses distinct spectral features, allowing one to monitor the enzyme-catalyzed reaction and its inhibition in real time. The utility of this sensitive fluorescence-monitored transformation for the high-throughput detection and analysis of ADA inhibitors is demonstrated.

Key concepts: Inosine, Chemistry, Adenosine deaminase, AMP deaminase, Biochemistry, Adenosine

Related papers

Back to paper searchBrowse research topicsOriginal source
Enzymatic Interconversion of Isomorphic Fluorescent Nucleosides: Adenosine Deaminase Transforms an Adenosine Analogue into an Inosine Analogue — Research Paper | ScholarLens