Strongly phosphorescent and water-soluble gold(I)-silver(I)-cysteine nanoplatelets via versatile small biomolecule cysteine-assisted synthesis for intracellular hypochlorite detection.

Abstract In biological systems, abnormal levels of hypochlorite (ClO−) could result in cell dysfunctions. Herein, we report a facile, one-step and green approach based on the versatile small biomolecule cysteine both serving as reducing agent and ligand for synthesizing the strongly photoluminencent and water-soluble Au(I)–Ag(I)-cysteine complexes nanoplatelets (Au(I)–Ag(I)-Cys nanoplatelets) for intracellular hypochlorite detection. Multiple spectroscopic and microscopical tools have been used to characterize the resultant Au(I)–Ag(I)-Cys nanoplatelets. It was found that with the cysteine-assisted synthesis approach, the Ag(I) doping to the Au(I) complexes could form the supramolecular organometallic nanoplatelets. Inside, the Au(I)–Ag(I) metallophilic interactions showing an Au to Ag charge transfer property were formed, thereby enhancing the photoluminescence (PL) intensity via the charge transfer from the bioligand's S to the metal-metal center. The quantum yield (QY) was measured to show a maximum 16-fold enhancement (i.e., from 0.85 to 13.8%). Interestingly, in the presence of ClO−, the metal-thiolate ligand structure of the as-synthesized Au(I)–Ag(I)-Cys nanoplatelets could be oxidatively damaged, causing the PL quenching, thereby producing the effect of biorecognition towards ClO− anions. The ClO−-induced PL quenching produced two linear regions at ClO− concentrations of 0.01–5.0 μM and 5.0–1000 μM with a limit of detection (LOD) of 8.0 nM (S/N = 3). The ClO−-induced PL quenching was specific over the other typical reactive oxygen species (ROS) and the potential interfering substances in biological samples. In addition, the Au(I)–Ag(I)-Cys nanoplatelets had good biocompatibility. Thus, they could be further developed as a biosensor for detecting endogenous ClO− anions in living cells.