Direct oxidative pathway from amplex red to resorufin revealed by in situ confocal imaging. Issue 37 (29th July 2016)

• Record Type: Journal Article
• Authors: Lefrançois, Pauline; Vajrala, Venkata Suresh Reddy; Arredondo, Imelda Bonifas; Goudeau, Bertrand; Doneux, Thomas; Bouffier, Laurent; Arbault, Stéphane
• Is Part Of: Physical chemistry chemical physics. Volume 18:Issue 37(2016)
• Page Start: 25817
• Page End: 25822
• Publication Date: 2016-07-29
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c6cp04438g
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : The conversion of Amplex Red (AR) to the fluorescent dye resorufin (RS) is employed in many biochemical assays. Here, direct generation of RS from AR at a mild oxidation potential is proven by a series of in situ electrochemical techniques. Abstract : 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 ( λ abs = 572 nm) and yields strong fluorescence ( λ fluo = 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.