DNA
DNA甲基化
核酸外切酶 III
化学
甲基化DNA免疫沉淀
分子信标
生物物理学
核酸外切酶
生物化学
检出限
分子生物学
DNA聚合酶
生物
寡核苷酸
基因
色谱法
基因表达
大肠杆菌
作者
Qiumei Feng,Qin Li,Mengying Wang,Po Wang
标识
DOI:10.1016/j.bios.2019.111847
摘要
A promising electrochemical system was explored for DNA methylation detection according to the construction of a signal-on biosensor. Based on the ingenious design of probe DNA and auxiliary DNA, methylated target DNA triggered the exonuclease III (Exo III) digestion of auxiliary DNA from 3'-terminus, resulting in the conformational change of probe DNA with an electroactive methylene blue (MB) tag at 5'-terminus. Consequently, the MB tag in the probe DNA was close to the electrode surface for electron transfer, generating an increased current signal. Because of the target recycling of methylated DNA, significant signal amplification was obtained. Moreover, bisulfite conversion conferred an efficient approach for the universal analysis of any CpG sites without the restriction of specific DNA sequence. As a result, the target DNA with different methylation statuses were clearly recognized, and the fully methylated DNA was quantified in a wide range from 10 fM to 100 pM, with a detection limit of 4 fM. The present work realized the assay of methylated target DNA in serum samples with satisfactory results, illustrating the application performance of the system in complex sample matrix.
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