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首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >A simple and universal electrochemical assay for sensitive detection of DNA methylation, methyltransferase activity and screening of inhibitors
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A simple and universal electrochemical assay for sensitive detection of DNA methylation, methyltransferase activity and screening of inhibitors

机译:用于敏感DNA甲基化,甲基转移酶活性和抑制剂筛选的简单且通用的电化学测定

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摘要

Many studies have confirmed that DNA methylation is highly correlated with the occurrence and development of various diseases including cancers. In this work, we developed a simple, sensitive, selective, and universal electrochemical biosensor for detection of DNA methylation and assay of DNA methyltransferase (MTase) activity using M.SssI MTase as an example. The thiolated single-stranded DNA SI was self-assembled on the surface of gold nanoparticles deposition modified glassy carbon electrode via Au-S bonding, then hybridization between the DNA S1 and its complementary DNA S2 formed a double-stranded target sequence for both M.SssI MTase and restriction endonuclease HpaII. HpaII could not cleave the target sequence after it was methylated by M.SssI MTase, while the sequence without methylation could be cleaved. Here, we used methylene blue (MB) as electrochemical indicator. The electrochemical signal of MB increased linearly with increasing M.SssI MTase concentration from 0.5 to 25 U/mL and from 25 to 400 U/mL with a detection limit of 0.04 U/mL. Moreover, screening of M.SssI MTase inhibitors 5-azacytidine (5-Aza) and 5-Aza-2'-deoxycytidine (5-Aza-dC) were successfully investigated using the fabricated electrochemical biosensor and showed that the two classic drugs could both inhibit the M.SssI MTase activity with the IC50 of 2.8 mu M and 0.37 mu M, respectively, indicating potential application in discovery of new anticancer drugs.
机译:许多研究证实,DNA甲基化与包括癌症的各种疾病的发生和发展高度相关。在这项工作中,我们开发了一种简单,灵敏,选择性和通用的电化学生物传感器,用于检测使用M.SSSI MTase作为实例的DNA甲基转移酶(MTase)活性的DNA甲基化和测定。通过AU-S键合在金纳米颗粒沉积改性玻璃电极的表面上自组装,然后在DNA S1及其互补DNA S2之间杂交形成双链靶序列。 SSSI MTase和限制性内切核酸酶HPAII。 HPAII不能在M.SSSI MTase甲基化后切割靶序列,而无需甲基化的序列可以裂解。在这里,我们用亚甲蓝(MB)作为电化学指示剂。 MB的电化学信号随着0.5至25u / ml的增加,从0.04 u / ml的检测限为0.5至25u / ml的M.SSSI MTase浓度增加。此外,使用制造的电化学生物传感器成功地研究了M.SSSI MTase抑制剂5-氮杂胞苷(5-AZA)和5-AZA-2'-脱氧胞苷(5-AZA-DC)的筛选,并显示了两种经典药物都可以分别抑制M.SSI mTase活性,分别用IC50和0.37μm,表明在发现新的抗癌药物中的潜在应用。

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