Protein-stabilized gold nanoclusters (AuNCs) are intensively used in nanoscale biological systems and biosensors. However, protein-stabilized AuNCs that exhibit an emission peak at the first near-infrared (NIR) window (700–900 nm) have rarely been explored. Herein, we present a rapid microwave synthetic approach for developing NIR-emissive AuNCs (named NIR750-AuNCs) through pH-mediated NaBH 4 reduction of HAuCl 4 in the presence of lysozyme as a template. The NIR750-AuNCs exhibited emission peaks at 750 nm with luminescence lifetimes of 1.0 μs and quantum yields (QY) of 4.9%. The incorporation of Ag(I) into NIR750-AuNCs [named [email protected] (I)] efficiently enhanced their QY (13.7%) and luminescence lifetime (1.9 μs) due to the coordination of the Ag(I) ions with electron-rich residues of the lysozyme shell that mediates the ligand-to-metal–metal charge transfer (LMMCT) process. Additionally, this coordination reaction enables [email protected] (I) to exhibit excellent resistance to photobleaching. The lysozyme shell allowed the conjugation of [email protected] (I) with FITC molecules. As a result, the as-made FITC/ [email protected] (I) display two well-resolved emission peaks at 525 and 750 nm with almost equal intensities. These outstanding features allowed the use of FITC/ [email protected] (I) for ratiometric sensing of 5–25 μM NaHS in environmental samples with an excellent reproducibility (relative standard deviation of intensity ratio (<2.5%), satisfactory selectivity, and acceptable recovery (94.4%–101.9%). The sensing mechanism of FITC/ [email protected] (I) is attributable to HS – -triggered removal of Ag(I) from the electron-rich residues of the lysozyme shell. Also, FITC/ [email protected] (I) were implemented for ratiometric imaging of exogenous and endogenous H 2 S in live cells. This work demonstrates the synthesis of protein-stabilized AuNCs with an emission maximum of 750 nm, paving the road to designing NIR-emitting AuNCs.
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Chuang et al. (2022) studied this question.
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