Institute of Biotechnology, Helsinki Institute of Life Science (HiLIFE), University of Helsinki, Helsinki 00014, Finland.
Center for Life Sciences, National Laboratory Astana, Nazarbayev University, Astana 010000, Kazakhstan.
Anal Chem. 2023 Dec 5;95(48):17818-17825. doi: 10.1021/acs.analchem.3c03894. Epub 2023 Nov 22.
Long-read sequencing technologies require high-molecular-weight (HMW) DNA of sufficient purity and integrity, which can be difficult to obtain from complex biological samples. We propose a method for purifying HMW DNA that takes advantage of the fact that DNA's electrophoretic mobility decreases in a high-ionic-strength environment. The method begins with the separation of HMW DNA from various impurities by electrophoresis in an agarose gel-filled channel. After sufficient separation, a high-salt gel block is placed ahead of the DNA band of interest, leaving a gap between the separating gel and the high-salt gel that serves as a reservoir for sample collection. The DNA is then electroeluted from the separating gel into the reservoir, where its migration slows due to electrostatic shielding of the DNA's negative charge by excess counterions from the high-salt gel. As a result, the reservoir accumulates HMW DNA of high purity and integrity, which can be easily collected and used for long-read sequencing and other demanding applications without additional desalting. The method is simple and inexpensive, yields sequencing-grade HMW DNA even from difficult plant and soil samples, and has the potential for automation and scalability.
长读测序技术需要具有足够纯度和完整性的高分子量 (HMW) DNA,而从复杂的生物样本中获得这种 DNA 非常困难。我们提出了一种从复杂生物样本中分离 HMW DNA 的方法,该方法利用了在高离子强度环境中 DNA 电泳迁移率降低的原理。该方法首先通过在充满琼脂糖凝胶的通道中进行电泳,将 HMW DNA 与各种杂质分离开来。在充分分离后,在感兴趣的 DNA 条带前放置一个高盐凝胶块,在分离胶和高盐胶之间留出一个间隙,作为样品收集的储液器。然后,DNA 通过电渗作用从分离胶转移到储液器中,由于高盐凝胶中的过量抗衡离子对 DNA 负电荷的静电屏蔽作用,DNA 的迁移速度减慢。结果,储液器中积累了具有高纯度和完整性的 HMW DNA,可以轻松收集并用于长读测序和其他苛刻的应用,而无需进一步脱盐。该方法简单且廉价,即使是来自困难的植物和土壤样本也能获得可用于测序的 HMW DNA,并且具有自动化和可扩展性的潜力。