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利用切口酶高效制备内部修饰的单分子构建体。

Efficient preparation of internally modified single-molecule constructs using nicking enzymes.

机构信息

Biotechnology Center, Technische Universität Dresden, D-01062 Dresden, Germany.

出版信息

Nucleic Acids Res. 2011 Feb;39(3):e15. doi: 10.1093/nar/gkq1004. Epub 2010 Nov 10.

Abstract

Investigations of enzymes involved in DNA metabolism have strongly benefited from the establishment of single molecule techniques. These experiments frequently require elaborate DNA substrates, which carry chemical labels or nucleic acid tertiary structures. Preparing such constructs often represents a technical challenge: long modified DNA molecules are usually produced via multi-step processes, involving low efficiency intermolecular ligations of several fragments. Here, we show how long stretches of DNA (>50 bp) can be modified using nicking enzymes to produce complex DNA constructs. Multiple different chemical and structural modifications can be placed internally along DNA, in a specific and precise manner. Furthermore, the nicks created can be resealed efficiently yielding intact molecules, whose mechanical properties are preserved. Additionally, the same strategy is applied to obtain long single-strand overhangs subsequently used for efficient ligation of ss- to dsDNA molecules. This technique offers promise for a wide range of applications, in particular single-molecule experiments, where frequently multiple internal DNA modifications are required.

摘要

研究 DNA 代谢相关的酶很大程度上受益于单分子技术的建立。这些实验通常需要精心设计的 DNA 底物,这些底物带有化学标记或核酸三级结构。制备这些构建体通常是一项技术挑战:长修饰的 DNA 分子通常通过多步过程产生,涉及几个片段之间效率低下的分子间连接。在这里,我们展示了如何使用切口酶修饰长链 DNA(>50bp)以产生复杂的 DNA 构建体。可以以特定且精确的方式在 DNA 内部的多个不同的化学和结构修饰。此外,有效地重新封闭所产生的切口,从而产生完整的分子,其机械性能得以保留。此外,还应用相同的策略来获得随后用于有效连接 ss-DNA 分子的长单链突出端。该技术具有广泛的应用前景,特别是在需要多个内部 DNA 修饰的单分子实验中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f83/3035433/6e1575512d2f/gkq1004f1.jpg

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