Candelli Andrea, Hoekstra Tjalle P, Farge Geraldine, Gross Peter, Peterman Erwin J G, Wuite Gijs J L
Institute for Lasers, Life and Biophotonics, Department of Physics and Astronomy, VU University Amsterdam, Amsterdam, 1081, HV, The Netherlands.
Biopolymers. 2013 Sep;99(9):611-20. doi: 10.1002/bip.22225.
Essential genomic transactions such as DNA-damage repair and DNA replication take place on single-stranded DNA (ssDNA) or require specific single-stranded/double-stranded DNA (ssDNA/dsDNA) junctions (SDSJ). A significant challenge in single-molecule studies of DNA-protein interactions using optical trapping is the design and generation of appropriate DNA templates. In contrast to dsDNA, only a limited toolbox is available for the generation of ssDNA constructs for optical tweezers experiments. Here, we present several kinds of DNA templates suitable for single-molecule experiments requiring segments of ssDNA of several kilobases in length. These different biotinylated dsDNA templates can be tethered between optically trapped microspheres and can, by the subsequent use of force-induced DNA melting, be converted into partial or complete ssDNA molecules. We systematically investigated the time scale and efficiency of force-induced melting at different ionic strengths for DNA molecules of different sequences and lengths. Furthermore, we quantified the impact of microspheres of different sizes on the lifetime of ssDNA tethers in optical tweezers experiments. Together, these experiments provide deeper insights into the variables that impact the production of ssDNA for single molecules studies and represent a starting point for further optimization of DNA templates that permit the investigation of protein binding and kinetics on ssDNA.
诸如DNA损伤修复和DNA复制等基本的基因组事务发生在单链DNA(ssDNA)上,或者需要特定的单链/双链DNA(ssDNA/dsDNA)连接点(SDSJ)。利用光镊进行DNA-蛋白质相互作用的单分子研究中的一个重大挑战是设计和生成合适的DNA模板。与双链DNA(dsDNA)相比,用于生成用于光镊实验的ssDNA构建体的工具非常有限。在这里,我们展示了几种适用于单分子实验的DNA模板,这些实验需要长度为几千碱基的ssDNA片段。这些不同的生物素化双链DNA模板可以连接在光镊捕获的微球之间,并且通过随后使用力诱导的DNA解链,可以转化为部分或完全的单链DNA分子。我们系统地研究了不同序列和长度的DNA分子在不同离子强度下力诱导解链的时间尺度和效率。此外,我们在光镊实验中量化了不同大小的微球对单链DNA系链寿命的影响。总之,这些实验为影响单分子研究中ssDNA产生的变量提供了更深入的见解,并代表了进一步优化DNA模板的起点,这些模板允许研究蛋白质与单链DNA的结合及动力学。