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一种基于磷酸柱[5]芳烃@多壁碳纳米管与硫堇之间的主客体识别用于T4多核苷酸激酶活性测定的电化学生物传感器。

An electrochemical biosensor for T4 polynucleotide kinase activity assay based on host-guest recognition between phosphate pillar[5]arene@MWCNTs and thionine.

作者信息

Su Aiwen, Luo Dan, Li Shixuan, Zhang Yanli, Wang Hongbin, Yang Lijuan, Yang Wenrong, Pang Pengfei

机构信息

Key Laboratory of Environmental Functional Materials of Yunnan Province Education Department, Yunnan Minzu University, Kunming 650504, P. R. China.

School of Life and Environmental Sciences, Deakin University, Geelong, VIC 3217, Australia.

出版信息

Analyst. 2024 Feb 12;149(4):1271-1279. doi: 10.1039/d3an01863f.

DOI:10.1039/d3an01863f
PMID:38226548
Abstract

T4 polynucleotide kinase helps with DNA recombination and repair. In this study, an electrochemical biosensor was developed for a T4 polynucleotide kinase activity assay and inhibitor screening based on phosphate pillar[5]arene and multi-walled carbon nanotube nanocomposites. The water-soluble pillar[5]arene was employed as the host to complex thionine guest molecules. The substrate DNA with a 5'-hydroxyl group initially self-assembled on the gold electrode surface through chemical adsorption of the thiol group, which was phosphorylated in the presence of T4 polynucleotide kinase. Titanium dioxide nanoparticles served as a bridge to link phosphorylated DNA and phosphate pillar[5]arene and multi-walled carbon nanotube composite due to strong phosphate-Ti-phosphate chemistry. Through supramolecular host-guest recognition, thionine molecules were able to penetrate the pillar[5]arene cavity, resulting in an enhanced electrochemical response signal. The electrochemical signal is proportional to the T4 polynucleotide kinase concentration in the range of 10 to 15 U mL with a detection limit of 5 × 10 U mL. It was also effective in measuring HeLa cell lysate-related T4 polynucleotide kinase activity and inhibitor screening. The proposed method offers a unique sensing platform for kinase activity measurement, holding great potential in nucleotide kinase-target drug development, clinical diagnostics, and inhibitor screening.

摘要

T4多核苷酸激酶有助于DNA重组和修复。在本研究中,基于磷酸柱[5]芳烃和多壁碳纳米管纳米复合材料,开发了一种用于T4多核苷酸激酶活性测定和抑制剂筛选的电化学生物传感器。水溶性柱[5]芳烃用作主体,用于络合硫堇客体分子。具有5'-羟基的底物DNA最初通过硫醇基团的化学吸附自组装在金电极表面,在T4多核苷酸激酶存在下被磷酸化。由于强的磷酸-钛-磷酸化学作用,二氧化钛纳米颗粒作为桥梁连接磷酸化的DNA和磷酸柱[5]芳烃与多壁碳纳米管复合材料。通过超分子主客体识别,硫堇分子能够穿透柱[5]芳烃空腔,从而增强电化学响应信号。在10至15 U/mL范围内,电化学信号与T4多核苷酸激酶浓度成正比,检测限为5×10 U/mL。它还可有效测量与HeLa细胞裂解物相关的T4多核苷酸激酶活性并进行抑制剂筛选。所提出的方法为激酶活性测量提供了一个独特的传感平台,在核苷酸激酶靶向药物开发、临床诊断和抑制剂筛选方面具有巨大潜力。

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