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外切核酸酶 III 在微阵列上的作用:荧光相关光谱法观察 DNA 降解。

Exonuclease III action on microarrays: observation of DNA degradation by fluorescence correlation spectroscopy.

机构信息

Physics Institute, University of Lübeck, D-23538 Lübeck, Germany.

出版信息

Anal Biochem. 2010 Apr 15;399(2):251-6. doi: 10.1016/j.ab.2009.12.004. Epub 2010 Jan 6.

Abstract

DNA with all cytosines, thymines, or all pyrimidines of one strand substituted by fluorescently labeled analogs shows diminished solubility in aqueous media and a strong tendency to aggregation that hampers enzymatic downstream processing. In this study, immobilization of fully fluorescently labeled DNA on microarrays was shown to resolve the named problems and to enable successive DNA degradation by exonuclease III. Fluorescence correlation spectroscopy and single-molecule counting for monitoring the course of DNA hydrolysis in real time revealed the virtually processive degradation of labeled DNA that occurred at an average rate of approximately 4 nt/s.

摘要

DNA 中所有胞嘧啶、胸腺嘧啶或一条链上的所有嘧啶都被荧光标记的类似物取代,会降低在水性介质中的溶解度,并强烈倾向于聚集,从而阻碍酶的下游处理。在这项研究中,证明了完全荧光标记的 DNA 在微阵列上的固定可以解决上述问题,并能够通过外切酶 III 进行连续的 DNA 降解。荧光相关光谱和单分子计数实时监测 DNA 水解过程,揭示了标记 DNA 的几乎连续的降解,其平均速率约为 4 个核苷酸/秒。

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