{"title":"Distinct DNA conformations during forward and backward translocations through a conical nanopore†","authors":"Fei Zheng and Quan Han","doi":"10.1039/D4AN01068J","DOIUrl":null,"url":null,"abstract":"<p >DNA conformations, which encompass the three-dimensional structures of the DNA strand, play a crucial role in genome regulation. During DNA translocation in a nanopore, various conformations occur due to interactions among force fields, the fluidic environment, and polymer features. The most common conformation is folding, where DNA moves through the nanopore in a two-strand or multi-strand manner, influencing the current signature. Factors such as hydrodynamic drag, ionic environments, and DNA length significantly affect these conformations. Notably, conical nanopores, with their asymmetrical geometry, impose unique constraints on DNA translocation. Our findings reveal that during forward translocation, from the narrow (<em>cis</em>) end to the wide (<em>trans</em>) end, DNA experiences less resistance, resulting in shorter translocation times and higher blockade currents. Conversely, backward translocation, from the wide (<em>trans</em>) end to the narrow (<em>cis</em>) end, leads to longer translocation times and more complex conformations due to increased hydrodynamic drag and geometric constraints. This study employs molecular ping-pong methods to confine DNA, further highlighting the intricate dynamics of DNA folding within nanopores. These insights enhance the understanding of DNA behavior in confined environments, contributing to advancements in nanopore-based sensing and sequencing technologies, with implications for genome regulation and biomedical applications.</p>","PeriodicalId":63,"journal":{"name":"Analyst","volume":" 20","pages":" 5131-5138"},"PeriodicalIF":3.6000,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/an/d4an01068j?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analyst","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/an/d4an01068j","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
DNA conformations, which encompass the three-dimensional structures of the DNA strand, play a crucial role in genome regulation. During DNA translocation in a nanopore, various conformations occur due to interactions among force fields, the fluidic environment, and polymer features. The most common conformation is folding, where DNA moves through the nanopore in a two-strand or multi-strand manner, influencing the current signature. Factors such as hydrodynamic drag, ionic environments, and DNA length significantly affect these conformations. Notably, conical nanopores, with their asymmetrical geometry, impose unique constraints on DNA translocation. Our findings reveal that during forward translocation, from the narrow (cis) end to the wide (trans) end, DNA experiences less resistance, resulting in shorter translocation times and higher blockade currents. Conversely, backward translocation, from the wide (trans) end to the narrow (cis) end, leads to longer translocation times and more complex conformations due to increased hydrodynamic drag and geometric constraints. This study employs molecular ping-pong methods to confine DNA, further highlighting the intricate dynamics of DNA folding within nanopores. These insights enhance the understanding of DNA behavior in confined environments, contributing to advancements in nanopore-based sensing and sequencing technologies, with implications for genome regulation and biomedical applications.
DNA 构象包括 DNA 链的三维结构,在基因组调控中起着至关重要的作用。DNA 在纳米孔中转运时,由于力场、流体环境和聚合物特征之间的相互作用,会出现各种构象。最常见的构象是折叠,DNA 以双链或多链的方式通过纳米孔,影响电流特征。流体动力阻力、离子环境和 DNA 长度等因素都会对这些构象产生重大影响。值得注意的是,锥形纳米孔具有不对称的几何形状,对 DNA 的转位造成了独特的限制。我们的研究结果表明,在前向转位过程中,即从窄(顺式)端到宽(反式)端,DNA 遇到的阻力较小,因此转位时间较短,阻塞电流较大。相反,从宽(反式)端向窄(顺式)端逆向转位时,由于流体动力阻力和几何限制增加,转位时间更长,构象更复杂。该研究采用分子乒乓方法来限制 DNA,进一步突出了 DNA 在纳米孔内折叠的复杂动态。这些见解加深了人们对 DNA 在封闭环境中行为的理解,有助于推动基于纳米孔的传感和测序技术的发展,并对基因组调控和生物医学应用产生影响。