Enhancing Kinase Activity Detection with a Programmable Lanthanide Metal-Organic Framework via ATP-to-ADP Conversion.

IF 6.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL Analytical Chemistry Pub Date : 2024-07-23 Epub Date: 2024-07-11 DOI:10.1021/acs.analchem.4c02237
Long Yu, Yongjin Shen, Qi Xu, Zhiwen Gan, Yumin Feng, Chunxu Yang, Yuxiu Xiao
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Abstract

Precise modulation of host-guest interactions between programmable Ln-MOFs (lanthanide metal-organic frameworks) and phosphate analytes holds immense promise for enabling novel functionalities in biosensing. However, the intricate relationship between these functionalities and structures remains largely elusive. Understanding this correlation is crucial for advancing the rational design of fluorescent biosensor technology. Presently, there exists a large research gap concerning the utilization of Ln-MOFsto monitor the conversion of ATP to ADP, which poses a limitation for kinase detection. In this work, we delve into the potential of Ln-MOFs to amplify the fluorescence response during the kinase-mediated ATP-to-ADP conversion. Six Eu-MOFs were synthesized and Eu-TPTC ([1,1':4',1″]-terphenyl-3,3'',5,5''-tetracarboxylic acid) was selected as a ratiometric fluorescent probe, which is most suitable for high-precision detection of creatine kinase activity through the differential response from ATP to ADP. The molecular -level mechanism was confirmed by density functional theory. Furthermore, a simple paper chip-based platform was constructed to realize the fast (20 min) and sensitive (limit of detection is 0.34 U/L) creatine kinase activity detection in biological samples. Ln-MOF-phosphate interactions offer promising avenues for kinase activity assays and hold the potential for precise customization of analytical chemistry.

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通过 ATP 到ADP 的转换,利用可编程镧系金属有机框架增强激酶活性检测。
精确调节可编程 Ln-MOF(镧系元素金属有机框架)与磷酸盐分析物之间的主客体相互作用,为实现生物传感的新功能带来了巨大希望。然而,这些功能性与结构之间错综复杂的关系在很大程度上仍然难以捉摸。了解这种关系对于推进荧光生物传感器技术的合理设计至关重要。目前,在利用 Ln-MOF 监测 ATP 向 ADP 的转化方面还存在很大的研究空白,这对激酶检测造成了限制。在这项工作中,我们深入研究了 Ln-MOFs 在激酶介导的 ATP 向 ADP 转化过程中放大荧光响应的潜力。我们合成了六种 Eu-MOFs 并选择了 Eu-TPTC ([1,1':4',1″]-三联苯-3,3'',5,5''-四羧酸)作为比率计量荧光探针,它最适合通过 ATP 到 ADP 的差异响应来高精度检测肌酸激酶的活性。密度泛函理论证实了这一分子水平的机制。此外,还构建了一个基于纸芯片的简易平台,实现了生物样品中肌酸激酶活性的快速(20 分钟)和灵敏(检测限为 0.34 U/L )检测。Ln-MOF 与磷酸的相互作用为激酶活性检测提供了前景广阔的途径,并为精确定制分析化学提供了潜力。
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来源期刊
Analytical Chemistry
Analytical Chemistry 化学-分析化学
CiteScore
12.10
自引率
12.20%
发文量
1949
审稿时长
1.4 months
期刊介绍: Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.
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