化学
多巴胺
半胱氨酸
荧光
过氧化物酶
水溶液
拟南芥
检出限
硫醇
生物物理学
核化学
生物化学
酶
有机化学
色谱法
神经科学
生物
物理
量子力学
基因
突变体
作者
Zhengquan Yan,Yulian Tang,Zhaoran Zhang,Jing Feng,Junkai Hao,Shuo Sun,Meng Li,Yuguang Song,Wei Dong,Lei Hu
标识
DOI:10.1021/acs.analchem.4c00081
摘要
To boost the enzyme-like activity, biological compatibility, and antiaggregation effect of noble-metal-based nanozymes, folic-acid-strengthened Ag–Ir quantum dots (FA@Ag–Ir QDs) were developed. Not only did FA@Ag–Ir QDs exhibit excellent synergistic-enhancement peroxidase-like activity, high stability, and low toxicity, but they could also promote the lateral root propagation of Arabidopsis thaliana. Especially, ultratrace cysteine or Hg2+ could exclusively strengthen or deteriorate the inherent fluorescence property with an obvious "turn-on" or "turn-off" effect, and dopamine could alter the peroxidase-like activity with a clear hypochromic effect from blue to colorless. Under optimized conditions, FA@Ag–Ir QDs were successfully applied for the turn-on fluorescence imaging of cysteine or the stress response in cells and plant roots, the turn-off fluorescence monitoring of toxic Hg2+, or the visual detection of dopamine in aqueous, beverage, serum, or medical samples with low detection limits and satisfactory recoveries. The selective recognition mechanisms for FA@Ag–Ir QDs toward cysteine, Hg2+, and dopamine were illustrated. This work will offer insights into constructing some efficient nanozyme sensors for multichannel environmental analyses, especially for the prediagnosis of cysteine-related diseases or stress responses in organisms.
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