材料科学
双模
生物传感器
假阳性悖论
生物分析
生物分子
可靠性(半导体)
机制(生物学)
DNA
DNA损伤
纳米技术
计算生物学
电子工程
人工智能
生物化学
功率(物理)
计算机科学
生物
工程类
物理
量子力学
作者
Ji‐Na Hao,Yongsheng Li
标识
DOI:10.1002/adfm.201903058
摘要
Abstract The identification of biomolecules for disease diagnosis requires facile analytical technologies with high precision and reliability. Several signal transduction pathways have inspired the development of various bioanalytical systems. However, most systems are greatly limited by a single‐mechanism/mode assay, which easily results in false‐positive/negative results. Herein, a multiple‐mechanism‐driven optical biosensor for 8‐oxo‐2′‐deoxyguanosine (8‐oxo‐dG), an early pathological signature of DNA lesions and various diseases, is designed by assembling adenine as a recognition element, mellitic acid as energy donors and Eu 3+ as signal reporters into one metal‐organic framework (MOF) system. Significantly, by regulating the delicate competition between the different mechanisms, the fabricated single platform (Eu‐ade‐MOF) concurrently provides two switchable approaches for rapid qualitative (30 s and 4 min) and quantitive (ppb level) recognition of 8‐oxo‐dG in both complex artificial and real human urine environments. Compared with those single‐mechanism/mode‐driven detections, this light‐operated dual‐mode analysis system can inherently boost the analysis reliability and largely minimize the chances of false negatives/positives for a non‐invasive diagnosis of DNA damage and related diseases. This work represents the first effort in designing a luminescent sensor coupling multiple mechanisms in a single interface to determine DNA damage degree and provides a new approach for developing multimode analysis platforms for human health monitoring.
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