Cellular membrane-anchored fluorescent probe with aggregation-induced emission characteristics for selective detection of Cu2+ ions. (25th November 2016)

• Record Type: Journal Article
• Authors: Liu, Danni; Ji, Shenglu; Li, Heran; Hong, Liang; Kong, Deling; Qi, Xin; Ding, Dan
• Is Part Of: Faraday discussions. Volume 196(2017)
• Page Start: 377
• Page End: 393
• Publication Date: 2016-11-25
• Subjects: Chemistry -- Periodicals; Metallurgy -- Periodicals; Electrochemistry -- Periodicals; 540
• DOI: 10.1039/c6fd00176a
• Languages: English
• ISSNs: 1359-6640

Abstract

Abstract : The exploration of advanced fluorescent probes that can detect divalent copper (Cu 2+ ) in aqueous environments and even in live organisms is particularly valuable for understanding the occurrence and development of Cu 2+ -related diseases. In this work, we report the design and synthesis of an aggregation-induced emission luminogen (AIEgen)-based probe (TPE-Py-EEGTIGYG) by integrating an AIEgen, TPE-Py, with a peptide, EEGTIGYG, which can selectively detect Cu 2+ in both aqueous solution and live cells. Peptide EEGTIGYG has dual functionality in the probe design, namely improving water solubility and providing specific cell membrane-binding ability. TPE-Py-EEGTIGYG can self-assemble into nanoaggregates at high concentration in aqueous solution ( e.g., 25 μM), which possess large fluorescence output due to the restriction of intramolecular rotation of the phenyl rings on TPE-Py. The fluorescence of the TPE-Py-EEGTIGYG nanoaggregates can be significantly quenched by Cu 2+ but not by other metal ions, achieving the selective detection of Cu 2+ in aqueous media. Furthermore, TPE-Py-EEGTIGYG can exist as a molecular species and is very weakly fluorescent in dilute aqueous solution ( e.g., 5 μM), but can however largely switch on its fluorescence upon specifically anchoring onto the cell membrane. The emissive probes on the cell membrane can be used for the detection of Cu 2+ ions that move in and out of cells with a fluorescence "turn-off" mode.