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高效的 DNA 构建体金标装配用于单分子力谱学和成像。

Efficient golden gate assembly of DNA constructs for single molecule force spectroscopy and imaging.

机构信息

The Francis Crick Institute, London NW1 1AT, UK.

出版信息

Nucleic Acids Res. 2022 Jul 22;50(13):e77. doi: 10.1093/nar/gkac300.

Abstract

Single-molecule techniques such as optical tweezers and fluorescence imaging are powerful tools for probing the biophysics of DNA and DNA-protein interactions. The application of these methods requires efficient approaches for creating designed DNA structures with labels for binding to a surface or microscopic beads. In this paper, we develop a simple and fast technique for making a diverse range of such DNA constructs by combining PCR amplicons and synthetic oligonucleotides using golden gate assembly rules. We demonstrate high yield fabrication of torsionally-constrained duplex DNA up to 10 kbp in length and a variety of DNA hairpin structures. We also show how tethering to a cross-linked antibody substrate significantly enhances measurement lifetime under high force. This rapid and adaptable fabrication method streamlines the assembly of DNA constructs for single molecule biophysics.

摘要

单分子技术,如光学镊子和荧光成像,是探测 DNA 和 DNA-蛋白质相互作用的生物物理学的有力工具。这些方法的应用需要有效的方法来创建具有标记的设计 DNA 结构,以便与表面或微小珠结合。在本文中,我们开发了一种简单快速的技术,通过使用金纳米颗粒门组装规则将 PCR 扩增子和合成寡核苷酸结合,来制造各种此类 DNA 构建体。我们证明了高达 10 kbp 长度的扭转约束双链 DNA 和各种 DNA 发夹结构的高产率制造。我们还展示了如何将其连接到交联的抗体底物上,可显著提高高力下的测量寿命。这种快速且适应性强的制造方法简化了单分子生物物理学中 DNA 构建体的组装。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a76/9303394/6ae2caa3cfcc/gkac300fig1.jpg

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