{"title":"Trajectory Retracing of the Packaging and Ejection Processes of Coaxially Spooled DNA.","authors":"Chung Bin Park, Bong June Sung","doi":"10.1021/acs.jctc.5c00137","DOIUrl":null,"url":null,"abstract":"<p><p>The coaxial spool structure of DNA has been regarded as an equilibrium conformation inside of a viral capsid. It has also been accepted that the DNA conformation inside the viral capsid should correlate strongly with the ejection of DNA out of the viral capsid. However, how the coaxial spool structure of DNA would affect the ejection kinetics remains elusive at the molecular level. In this study, we perform extensive Langevin dynamics simulations for a single polymer chain packaged within a small confinement to mimic the packaging and ejection processes of viral DNA and investigate the effects of its conformation on the ejection kinetics. We show that when the polymer chain within a small rectangular confinement is coaxially spooled, its ejection kinetics is facilitated significantly due to the <i>trajectory retracing</i>. We tune the conformation of the polymer chain inside the confinement by changing both the chain rigidity and the aspect ratio (γ) of the confinement. As either the aspect ratio (γ) decreases or the rigidity increases, the chain packaged inside the confinement is more likely to have a coaxial spool structure. And the polymer chain of the coaxial spool structure ejects quickly than chains of other conformations. We find that the coaxial spool structure enables the single chain to follow the reverse pathway of the packaging during ejection without significant structural rearrangement, thus enhancing the ejection kinetics.</p>","PeriodicalId":45,"journal":{"name":"Journal of Chemical Theory and Computation","volume":" ","pages":"5736-5745"},"PeriodicalIF":5.7000,"publicationDate":"2025-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Theory and Computation","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.jctc.5c00137","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/27 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The coaxial spool structure of DNA has been regarded as an equilibrium conformation inside of a viral capsid. It has also been accepted that the DNA conformation inside the viral capsid should correlate strongly with the ejection of DNA out of the viral capsid. However, how the coaxial spool structure of DNA would affect the ejection kinetics remains elusive at the molecular level. In this study, we perform extensive Langevin dynamics simulations for a single polymer chain packaged within a small confinement to mimic the packaging and ejection processes of viral DNA and investigate the effects of its conformation on the ejection kinetics. We show that when the polymer chain within a small rectangular confinement is coaxially spooled, its ejection kinetics is facilitated significantly due to the trajectory retracing. We tune the conformation of the polymer chain inside the confinement by changing both the chain rigidity and the aspect ratio (γ) of the confinement. As either the aspect ratio (γ) decreases or the rigidity increases, the chain packaged inside the confinement is more likely to have a coaxial spool structure. And the polymer chain of the coaxial spool structure ejects quickly than chains of other conformations. We find that the coaxial spool structure enables the single chain to follow the reverse pathway of the packaging during ejection without significant structural rearrangement, thus enhancing the ejection kinetics.
期刊介绍:
The Journal of Chemical Theory and Computation invites new and original contributions with the understanding that, if accepted, they will not be published elsewhere. Papers reporting new theories, methodology, and/or important applications in quantum electronic structure, molecular dynamics, and statistical mechanics are appropriate for submission to this Journal. Specific topics include advances in or applications of ab initio quantum mechanics, density functional theory, design and properties of new materials, surface science, Monte Carlo simulations, solvation models, QM/MM calculations, biomolecular structure prediction, and molecular dynamics in the broadest sense including gas-phase dynamics, ab initio dynamics, biomolecular dynamics, and protein folding. The Journal does not consider papers that are straightforward applications of known methods including DFT and molecular dynamics. The Journal favors submissions that include advances in theory or methodology with applications to compelling problems.