荧光
检出限
化学
比色法
硫化氢
硫化物
生物传感器
选择性
牛血清白蛋白
环境化学
组合化学
色谱法
生物化学
硫黄
催化作用
有机化学
物理
量子力学
作者
Yong An,Linyu Li,Lepeng Li,Yongqiang Sun,Bo Li,Peng Wang
标识
DOI:10.1016/j.jhazmat.2023.133192
摘要
Pollution caused by Copper and hydrogen sulfide pollution has severe adverse effects on the environment and organisms. Real-time, fast and accurate monitoring of Cu2+ and S2- faces serious challenges. In this study, we designed a novel biosensor and synthesized it by mimicking the structure of the main Cu(II)-binding site on bovine serum albumin. As a peptide-based sensor, FGGH (FITC-Gly-Gly-His-NH2) can perform the sequential detection of Cu2+ and S2– by fluorescence and colorimetry. The high water solubility and selectivity make it suitable for monitoring Cu2+ and S2– in environmental water samples with high sensitivity; its limit of detection (LOD) is as low as 1.42 nM for Cu2+ and 22.2 nM for S2–. The paper-based sensing platform of this probe was found to be a promising tool for the on-site visualization of real-time quantitative analysis of Cu2+ and S2– due to its rapid response and recyclable detection characteristics. Additionally, FGGH was successfully used to image Cu2+ and S2– in living cells and zebrafish models with adequate fluorescence stability and low cytotoxicity, providing the first visual evidence of the effect of the interactions between Cu2+ and S2– on the redox homeostasis of organisms.
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