利用T4 DNA连接酶合成骨架修饰寡核苷酸

Q3 Biochemistry, Genetics and Molecular Biology Current protocols in chemical biology Pub Date : 2019-01-28 DOI:10.1002/cpch.62
Donaat Kestemont, Piet Herdewijn, Marleen Renders
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引用次数: 3

摘要

T4 DNA连接酶在高浓度的某些拥挤剂和辅质中催化一系列难以化学获得的骨架修饰寡核苷酸的合成。骨架修饰的核酸通常在酶和化学上更稳定,这使得它们作为潜在的诊断或治疗药物、生物安全工具或纳米技术很有趣。在本文中,我们描述了一个小规模的实验,以探索在3 M甜菜碱和10% PEG 8000存在下修饰寡核苷酸的连接反应效率,然后进行大规模的连接,随后分离连接的寡核苷酸。正确的产品形成可以用变性聚丙烯酰胺凝胶电泳和质谱进行验证。©2019 by John Wiley &儿子,Inc。
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Enzymatic Synthesis of Backbone-Modified Oligonucleotides Using T4 DNA Ligase

T4 DNA ligase in high concentrations of certain crowding agents and cosolutes catalyzes the synthesis of a series of backbone-modified oligonucleotides that are difficult to obtain chemically. Backbone-modified nucleic acids are often enzymatically and chemically more stable, making them interesting as potential diagnostic or therapeutic agents, as a biosafety tool, or in nanotechnology. In this article, we describe a small-scale experiment to probe the efficiency of the ligation reaction of modified oligonucleotides in the presence of 3 M betaine and 10% PEG 8000, followed by large-scale ligation with subsequent isolation of the ligated oligonucleotide. The correct product formation can be verified using denaturing polyacrylamide gel electrophoresis and mass spectrometry. © 2019 by John Wiley & Sons, Inc.

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Current protocols in chemical biology
Current protocols in chemical biology Biochemistry, Genetics and Molecular Biology-Biophysics
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