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采用N-乙二醛标记和MazF切割对FTO进行电化学检测。

Electrochemical detection of FTO with N-kethoxal labeling and MazF cleavage.

作者信息

Chen Chen, Zhao Mei, Guo Jingyi, Kuang Xia, Chen Zilin, Wang Fang

机构信息

School of Pharmaceutical Sciences, Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (MOE), Wuhan University Wuhan 430071 China

出版信息

RSC Adv. 2024 Aug 13;14(35):25561-25570. doi: 10.1039/d4ra03989k. eCollection 2024 Aug 12.

Abstract

6-Methyladenosine (m6A) is a prevalent modification in eukaryotic mRNAs and is linked to various human cancers. The fat mass and obesity-associated protein (FTO), a key m6A demethylase, is crucial in m6A regulation, affecting many biological processes and diseases. Detecting FTO is vital for clinical and research applications. Our study leverages the specific cleavage properties of the MazF endoribonuclease to design an electrochemical method with signal amplification guided by streptavidin-horseradish peroxidase (SA-HRP), intended for FTO detection. Initially, the compound N-kethoxal is employed for its reversible tagging ability, selectively attaching to guanine (G) bases. Subsequently, dibenzocyclooctyne polyethylene glycol biotin (DBCO-PEG4-Biotin), is introduced through a reaction with N-kethoxal. HRP is then employed to catalyze the redox system to enhance the current response further. A promising linear correlation between the peak current and the FTO concentration was observed within the range of 7.90 × 10 to 3.50 × 10 M, with a detection limit of 5.80 × 10 M. Moreover, this method assessed the FTO inhibitor FB23's inhibitory effect, revealing a final IC value of 54.73 nM. This result aligns with the IC value of 60 nM obtained through alternative methods and is very close to the values reported in the literature. The study provides reference value for research into obesity, diabetes, cancer, and other FTO-related diseases, as well as for the screening of potential therapeutic drugs.

摘要

6-甲基腺嘌呤(m6A)是真核生物mRNA中普遍存在的一种修饰,与多种人类癌症相关。脂肪量和肥胖相关蛋白(FTO)是一种关键的m6A去甲基化酶,在m6A调控中至关重要,影响许多生物学过程和疾病。检测FTO对临床和研究应用至关重要。我们的研究利用MazF内切核糖核酸酶的特异性切割特性,设计了一种以链霉亲和素-辣根过氧化物酶(SA-HRP)为信号放大引导的电化学方法,用于FTO检测。最初,化合物N-乙二醛因其可逆标记能力而被使用,选择性地附着于鸟嘌呤(G)碱基。随后,通过与N-乙二醛反应引入二苯并环辛炔聚乙二醇生物素(DBCO-PEG4-生物素)。然后使用HRP催化氧化还原系统以进一步增强电流响应。在7.90×10至3.50×10 M范围内观察到峰电流与FTO浓度之间有良好的线性相关性,检测限为5.80×10 M。此外,该方法评估了FTO抑制剂FB23的抑制作用,最终IC值为54.73 nM。该结果与通过其他方法获得的60 nM的IC值一致,并且与文献报道的值非常接近。该研究为肥胖、糖尿病、癌症和其他与FTO相关疾病的研究以及潜在治疗药物的筛选提供了参考价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2a0/11322896/911242cd17e9/d4ra03989k-s1.jpg

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