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A simple, universal colorimetric assay for endonuclease/methyltransferase activity and inhibition based on an enzyme-responsive nanoparticle system

机译:一种基于酶反应性纳米粒子系统的简单通用比色法,用于核酸内切酶/甲基转移酶活性和抑制

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摘要

An enzyme responsive nanoparticle system that uses a DNA-gold nanoparticle (AuNP) assembly as the substrate has been developed for the simple, sensitive, and universal monitoring of restriction endonucleases in real time. This new assay takes advantage of the palindromic recognition sequence of the restriction nucleases and the unique optical properties of AuNPs and is simpler than the procedure previously described by by Xu et al. (Angew. Chem. Int. Ed. Engl. 2007, 46, 3468-3470). Because it involves only one type of ssDNA modified AuNPs, this assay can be directed toward most of the endonucleases by simply changing the recognition sequence found within the linker DNA. In addition, the endonuclease activity could be quantitatively analyzed by the value of the reciprocal of hydrolysis half time (t_(1/2)~(-1)). Furthermore, our new design could also be applied to the assay of methyltransferase activity since the methylation of DNA inhibits its cleavage by the corresponding restriction endonuclease, and thus, this new methodology can be easily adapted to highthroughput screening of methyltransferase inhibitors.
机译:已经开发出一种以DNA-金纳米颗粒(AuNP)组件为底物的酶促响应纳米颗粒系统,用于实时,简单,灵敏,通用地监测限制性核酸内切酶。这种新的测定法利用限制性核酸酶的回文识别序列和AuNPs的独特光学性质,比Xu等人先前描述的方法更简单。 (Angew.Chem.Int.Ed.Engl.2007,46,3468-3470)。因为它仅涉及一种类型的ssDNA修饰的AuNP,所以可以通过简单地改变接头DNA中发现的识别序列,将这种测定法用于大多数核酸内切酶。另外,核酸内切酶活性可以通过水解半衰期的倒数(t_(1/2)〜(-1))进行定量分析。此外,我们的新设计还可以应用于甲基转移酶活性的测定,因为DNA的甲基化可通过相应的限制性核酸内切酶抑制其裂解,因此,这种新方法可轻松适用于甲基转移酶抑制剂的高通量筛选。

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