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Direct oxidative pathway from amplex red to resorufin revealed by in situ confocal imaging
Author(s) -
Pauline Lefrançois,
Venkata Suresh Vajrala,
Imelda Bonifas Arredondo,
Bertrand Goudeau,
Thomas Doneux,
Laurent Bouffier,
Stéphane Arbault
Publication year - 2016
Publication title -
physical chemistry chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 239
eISSN - 1463-9084
pISSN - 1463-9076
DOI - 10.1039/c6cp04438g
Subject(s) - in situ , fluorescence , chemistry , electrochemistry , redox , confocal , confocal microscopy , biophysics , photochemistry , electrode , biology , inorganic chemistry , optics , microbiology and biotechnology , organic chemistry , physics
Amplex Red (AR) is a very useful chemical probe that is employed in biochemical assays. In these assays, the non-fluorescent AR is converted to resorufin (RS), which strongly absorbs in the visible region (λabs = 572 nm) and yields strong fluorescence (λfluo = 583 nm). Even if AR is commonly used to report on enzymatic oxidase activities, an increasing number of possible interferences have been reported, thus lowering the accuracy of the so-called AR assay. As a redox-based reaction, we propose here to directly promote the conversion of AR to RS by means of electrochemistry. The process was first assessed by classic electrochemical and spectroelectrochemical investigations. In addition, we imaged the electrochemical conversion of AR to RS at the electrode surface by in situ confocal microscopy. The coupling of methodologies allowed to demonstrate that RS is directly formed from AR by an oxidation step, unlike what was previously reported. This gives a new insight in the deciphering of AR assays' mechanism and about their observed discrepancy.

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