纳米探针
光子上转换
限制
纳米技术
检出限
能量转移
化学
氨基酸
组合化学
材料科学
纳米颗粒
生物化学
有机化学
机械工程
工程类
离子
色谱法
分子物理学
作者
Yongan Tang,Xiaoyan Zhong,Shuangqian Yan,Xiaowang Liu,Liang Cheng,Yu Wang,Xiaogang Liu
标识
DOI:10.1002/anie.202105297
摘要
D-amino acids (DAAs) are indispensable in regulating diverse metabolic pathways. Selective and sensitive detection of DAAs is crucial for understanding the complexity of metabolic processes and managing associated diseases. However, current DAA detection strategies mainly rely on bulky instrumentation or electrochemical probes, limiting their cellular and animal applications. Here we report an enzyme-coupled nanoprobe that can detect enantiospecific DAAs through synergistic energy transfer. This nanoprobe offers near-infrared upconversion capability, a wide dynamic detection range, and a detection limit of 2.2 μM, providing a versatile platform for in vivo noninvasive detection of DAAs with high enantioselectivity. These results potentially allow real-time monitoring of biomolecular handedness in living animals, as well as developing antipsychotic treatment strategies.
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