Double protein directed synthesis of chemically etched sulfur doped quantum dots for signal "on-off-on" sensing of glutathione mediated by copper ions

In this study, a novel "on-off-on" fluorescent probe was suggested for sensitive and selective assay of glutathione (GSH). The as-fabricated nanoswitch employs a Cu 2+ -sulfur quantum dot system (SQ-dots/Cu 2+ ). The surface reactivity and water solubility of SQ-dots were improved through capping with egg white and bovine serum albumin proteins. The surface functional groups on the surface of double protein-protected SQ-dots enhanced the interaction with Cu 2+ ions, resulting in the aggregation induced quenching of SQ-dots. Addition of GSH, a strong Cu 2+ ion chelator, disassembles the large aggregates into relatively smaller ones, restoring the fluorescence emission of SQ-dots. Under optimized conditions, the fluorescence intensity was increased by increasing GSH amounts within the range of 0.13-550 μM with a detection limit (S/N = 3) of 0.04 μM. The SQ-dots/Cu 2+ system was successfully applied for the detection of GSH in different matrices such as dietary supplements, human serum, and vegetable extract samples. The as-fabricated probe holds great potential for the synthesis of other functionalized SQ-dots for (bio) sensing. A novel "on-off-on" Cu 2+ -sulfur quantum dot (weak fluorescence) system was suggested for detection of GSH. Addition of GSH disassembles the large aggregates into relatively smaller ones, restoring the fluorescence emission of SQ-dots.