Suppr超能文献

高产制备 DNA 和 RNA 构建体用于单分子力和扭矩光谱实验。

High-yield fabrication of DNA and RNA constructs for single molecule force and torque spectroscopy experiments.

机构信息

Junior Research Group 2, Interdisciplinary Center for Clinical Research, Friedrich Alexander University Erlangen-Nürnberg (FAU), Cauerstrasse 3, 91058 Erlangen, Germany.

出版信息

Nucleic Acids Res. 2019 Dec 16;47(22):e144. doi: 10.1093/nar/gkz851.

Abstract

Single molecule biophysics experiments have enabled the observation of biomolecules with a great deal of precision in space and time, e.g. nucleic acids mechanical properties and protein-nucleic acids interactions using force and torque spectroscopy techniques. The success of these experiments strongly depends on the capacity of the researcher to design and fabricate complex nucleic acid structures, as the outcome and the yield of the experiment also strongly depend on the high quality and purity of the final construct. Though the molecular biology techniques involved are well known, the fabrication of nucleic acid constructs for single molecule experiments still remains a difficult task. Here, we present new protocols to generate high quality coilable double-stranded DNA and RNA, as well as DNA and RNA hairpins with ∼500-1000 bp long stems. Importantly, we present a new approach based on single-stranded DNA (ssDNA) annealing and we use magnetic tweezers to show that this approach simplifies the fabrication of complex DNA constructs, such as hairpins, and converts more efficiently the input DNA into construct than the standard PCR-digestion-ligation approach. The protocols we describe here enable the design of a large range of nucleic acid construct for single molecule biophysics experiments.

摘要

单分子生物物理学实验能够在空间和时间上实现对生物分子的高精度观察,例如使用力和扭矩光谱技术研究核酸的机械性质和蛋白质-核酸相互作用。这些实验的成功在很大程度上取决于研究人员设计和制造复杂核酸结构的能力,因为实验的结果和产量也强烈依赖于最终构建体的高质量和高纯度。尽管涉及的分子生物学技术是众所周知的,但用于单分子实验的核酸构建体的制造仍然是一项困难的任务。在这里,我们提出了新的方案来生成高质量的可卷曲双链 DNA 和 RNA,以及具有约 500-1000 个碱基对长茎的 DNA 和 RNA 发夹。重要的是,我们提出了一种基于单链 DNA(ssDNA)退火的新方法,并使用磁镊证明这种方法简化了复杂 DNA 构建体(如发夹)的制造,并比标准的 PCR 消化-连接方法更有效地将输入 DNA 转化为构建体。我们在这里描述的方案能够为单分子生物物理学实验设计一系列的核酸构建体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e789/6902051/cb6858065107/gkz851fig1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验