Ratiometric fluorescent probe based on symmetric peptidyl receptor with picomolar affinity for Zn2+ in aqueous solution

• Published in: Sensors and actuators. B, Chemical Vol. 245; pp. 996 - 1003
• Main Authors: Mehta, Pramod Kumar, Oh, Eun-Taex, Park, Heon Joo, Lee, Keun-Hyeung
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01-06-2017
• Subjects: Chemosensor; Fluorescent; Probe; Ratiometric; Sensor; Zn2; Fluorescent; Chemosensor; Probe; Ratiometric; Zn2; Sensor
• ISSN: 0925-4005; 1873-3077
• DOI: 10.1016/j.snb.2017.01.154

•The fluorescent probe based on the peptide receptor with tunable binding affinities for Zn2+.•Highly sensitive ratiometric response to Zn2+ in aqueous solutions at physiological pH.•A picomolar binding affinity (300 pM) for Zn2+ in aqueous solutions and formation of a 1:1 complex.•Highly selective response to Zn2+ among various biological relevant metal ions.•Cell penetration and detection of intracellular Zn2+ in live cells.
It is still a significant challenge to synthesize ratiometric fluorescent probes based on the new receptor with potent and tunable binding affinities for Zn2+. A fluorescent probe (1) based on the symmetric peptide receptor bearing two imidazole and two sulfonamide groups was synthesized for the ratiometric detection of Zn2+ in aqueous solution. 1 selectively and sensitively detected Zn2+ among biological relevant metal ions by a ratiometric response. Upon addition of Zn2+, monomer emissions of the pyrenes at 379 and 399nm increased significantly and the excimer emission at 508nm decreased with a blue shift. About 1 equiv of Zn2+ ions completely induced the ratiometric response of 1. Job’s plot analysis indicated that 1 formed a 1:1 complex with Zn2+. The dissociation constant for Zn2+ was found to be 300 pM. The binding mode study revealed that two imidazole and two sulfonamide groups of the peptide receptor played an important role in the binding with Zn2+. The peptidyl probe successfully penetrated and detected intracellular Zn2+ in live cells.