Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an, 710069, PR China.
Shaanxi Key Laboratory of Catalysis, School of Chemistry and Environment Science, Shaanxi University of Technology, Hanzhong, Shaanxi, 723000, PR China.
Biosens Bioelectron. 2024 Jul 15;256:116276. doi: 10.1016/j.bios.2024.116276. Epub 2024 Apr 6.
Fat mass and obesity-associated protein (FTO) has gained attention as the first RNA N6-methyladenosine (mA) modification eraser due to its overexpression being associated with various cancers. In this study, an electrochemiluminescence (ECL) biosensor for the detection of demethylase FTO was developed based on DNAzyme-mediated CRISPR/Cas12a signal cascade amplification system and carboxylated carbon nitride nanosheets/phosphorus-doped nitrogen-vacancy modified carbon nitride nanosheets (C-CN/PCN) heterojunction as the emitter. The biosensor was constructed by modifying the C-CN/PCN heterojunction and a ferrocene-tagged probe (ssDNA-Fc) on a glassy carbon electrode. The presence of FTO removes the mA modification on the catalytic core of DNAzyme, restoring its cleavage activity and generating activator DNA. This activator DNA further activates the trans-cleavage ability of Cas12a, leading to the cleavage of the ssDNA-Fc and the recovery of the ECL signal. The C-CN/PCN heterojunction prevents electrode passivation and improves the electron-hole recombination, resulting in significantly enhanced ECL signal. The biosensor demonstrates high sensitivity with a low detection limit of 0.63 pM in the range from 1.0 pM to 100 nM. Furthermore, the biosensor was successfully applied to detect FTO in cancer cell lysate and screen FTO inhibitors, showing great potential in early clinical diagnosis and drug discovery.
脂肪量和肥胖相关蛋白(FTO)由于其过表达与各种癌症有关,因此作为第一个 RNA N6-甲基腺苷(mA)修饰清除剂而受到关注。在这项研究中,基于 DNAzyme 介导的 CRISPR/Cas12a 信号级联放大系统和羧基化碳氮纳米片/磷掺杂氮空位修饰碳氮纳米片(C-CN/PCN)异质结作为发射体,开发了一种用于检测去甲基酶 FTO 的电化学发光(ECL)生物传感器。该生物传感器通过修饰 C-CN/PCN 异质结和一个带有二茂铁标记的探针(ssDNA-Fc)在玻碳电极上构建。FTO 的存在去除了 DNAzyme 催化核心上的 mA 修饰,恢复了其切割活性并产生了激活 DNA。这种激活 DNA 进一步激活了 Cas12a 的转切割能力,导致 ssDNA-Fc 的切割和 ECL 信号的恢复。C-CN/PCN 异质结防止了电极钝化并提高了电子-空穴复合效率,从而显著增强了 ECL 信号。该生物传感器具有高灵敏度,在 1.0 pM 至 100 nM 的范围内检测限低至 0.63 pM。此外,该生物传感器成功地用于检测癌细胞裂解液中的 FTO 并筛选 FTO 抑制剂,在早期临床诊断和药物发现方面具有巨大的潜力。