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8-Azapurines as isosteric purine fluorescent probes for nucleic acid and enzymatic research.

Authors :
Wierzchowski J
Antosiewicz JM
Shugar D
Source :
Molecular bioSystems [Mol Biosyst] 2014 Nov; Vol. 10 (11), pp. 2756-74.
Publication Year :
2014

Abstract

The 8-azapurines, and their 7-deaza and 9-deaza congeners, represent a unique class of isosteric (isomorphic) analogues of the natural purines, frequently capable of substituting for the latter in many biochemical processes. Particularly interesting is their propensity to exhibit pH-dependent room-temperature fluorescence in aqueous medium, and in non-polar media. We herein review the physico-chemical properties of this class of compounds, with particular emphasis on the fluorescence emission properties of their neutral and/or ionic species, which has led to their widespread use as fluorescent probes in enzymology, including enzymes involved in purine metabolism, agonists/antagonists of adenosine receptors, mechanisms of catalytic RNAs, RNA editing, etc. They are also exceptionally useful fluorescent probes for analytical and clinical applications in crude cell homogenates.

Details

Language :
English
ISSN :
1742-2051
Volume :
10
Issue :
11
Database :
MEDLINE
Journal :
Molecular bioSystems
Publication Type :
Academic Journal
Accession number :
25124808
Full Text :
https://doi.org/10.1039/c4mb00233d