The Francis Crick Institute, London NW1 1AT, UK.
Nucleic Acids Res. 2022 Jul 22;50(13):e77. doi: 10.1093/nar/gkac300.
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.
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。