Issue 7, 2015

Tailoring of the desired selectivity and the turn-on detection range in a self-assembly-based fluorescence sensory system

Abstract

This study demonstrates how to control the selectivity and the turn-on detection range toward the tailoring of an assembly-based fluorescence (FL) sensory system. Assembly-based FL chemosensors composed of oligophenylenevinylene with a varied number of guanidinium receptors (G2, G4 and G6) were newly developed, and their FL response to nucleotides (AMP, ADP and ATP) was investigated. Indeed, G6 exhibited FL emission via self-assembly with ATP. More importantly, the FL response of G6 showed markedly improved selectivity for ATP over ADP and a broadly extended detection range of ATP concentration under adjusted salt conditions. The salt effect on the FL response revealed the competitive binding interactions affecting the subsequent self-assembly process. These studies have unveiled the pivotal binding mechanisms operating in the self-assembly process, which tailor the performance level of the assembly-based sensory system. We believe that this study offers a new design principle of an assembly-based FL chemosensor with high selectivity and the appropriate detection range, being different from the conventional key-and-lock system.

Graphical abstract: Tailoring of the desired selectivity and the turn-on detection range in a self-assembly-based fluorescence sensory system

Supplementary files

Article information

Article type
Edge Article
Submitted
10 Mar 2015
Accepted
08 Apr 2015
First published
06 May 2015
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2015,6, 3863-3867

Tailoring of the desired selectivity and the turn-on detection range in a self-assembly-based fluorescence sensory system

T. Noguchi, B. Roy, D. Yoshihara, Y. Tsuchiya, T. Yamamoto and S. Shinkai, Chem. Sci., 2015, 6, 3863 DOI: 10.1039/C5SC00863H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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