线性聚合物溶液中单分子DNA的顶点固定和拉伸

IF 12.1 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Small Pub Date : 2025-05-10 DOI:10.1002/smll.202503087
Kunlin Ma, Caleb J. Samuel, Soumyadeep Paul, Ray Chang, Fereshteh L. Memarian, Gabrielle Haddon-Vukasin, Armin Darvish, Juan G. Santiago
{"title":"线性聚合物溶液中单分子DNA的顶点固定和拉伸","authors":"Kunlin Ma,&nbsp;Caleb J. Samuel,&nbsp;Soumyadeep Paul,&nbsp;Ray Chang,&nbsp;Fereshteh L. Memarian,&nbsp;Gabrielle Haddon-Vukasin,&nbsp;Armin Darvish,&nbsp;Juan G. Santiago","doi":"10.1002/smll.202503087","DOIUrl":null,"url":null,"abstract":"<p>Trapping, linearization, and imaging of single-molecule DNA are of broad interest to both biophysicists who study polymer physics and engineers who build nucleic acid analysis methods such as optical mapping. In this study, single DNA molecules in a neutral linear polymer solution are driven with an axial electric field through microchannels, and their dynamics are studied using fluorescence microscopy. Above a certain threshold electric field, individual DNA molecules become pinned to the channel walls at a vertex on each molecule and are stretched in the direction opposite to electric field. Upon removal of the electric field, pinned DNA molecules undergo relaxation within a few seconds to a Brownian coil around the vertex. After tens of seconds, DNA is released and free to diffuse and electromigrate. The method enables high-quality imaging of single-molecule DNA with high throughput using simple-to-fabricate fluidic structures. The conditions required for trapping dynamics, relaxation dynamics, and the repeatability of vertex pinning are analyzed. It is hypothesized that the neutral linear (non-cross-linked) polymers adsorb to the wall and form scaffolds that trap DNA. Potential hypotheses are discussed based on the empirical findings to explain potential physical mechanism of such unique trapping behavior in a non-crosslinked linear polymer solution.</p>","PeriodicalId":228,"journal":{"name":"Small","volume":"21 25","pages":""},"PeriodicalIF":12.1000,"publicationDate":"2025-05-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Vertex Pinning and Stretching of Single Molecule DNA in a Linear Polymer Solution\",\"authors\":\"Kunlin Ma,&nbsp;Caleb J. Samuel,&nbsp;Soumyadeep Paul,&nbsp;Ray Chang,&nbsp;Fereshteh L. Memarian,&nbsp;Gabrielle Haddon-Vukasin,&nbsp;Armin Darvish,&nbsp;Juan G. Santiago\",\"doi\":\"10.1002/smll.202503087\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Trapping, linearization, and imaging of single-molecule DNA are of broad interest to both biophysicists who study polymer physics and engineers who build nucleic acid analysis methods such as optical mapping. In this study, single DNA molecules in a neutral linear polymer solution are driven with an axial electric field through microchannels, and their dynamics are studied using fluorescence microscopy. Above a certain threshold electric field, individual DNA molecules become pinned to the channel walls at a vertex on each molecule and are stretched in the direction opposite to electric field. Upon removal of the electric field, pinned DNA molecules undergo relaxation within a few seconds to a Brownian coil around the vertex. After tens of seconds, DNA is released and free to diffuse and electromigrate. The method enables high-quality imaging of single-molecule DNA with high throughput using simple-to-fabricate fluidic structures. The conditions required for trapping dynamics, relaxation dynamics, and the repeatability of vertex pinning are analyzed. It is hypothesized that the neutral linear (non-cross-linked) polymers adsorb to the wall and form scaffolds that trap DNA. Potential hypotheses are discussed based on the empirical findings to explain potential physical mechanism of such unique trapping behavior in a non-crosslinked linear polymer solution.</p>\",\"PeriodicalId\":228,\"journal\":{\"name\":\"Small\",\"volume\":\"21 25\",\"pages\":\"\"},\"PeriodicalIF\":12.1000,\"publicationDate\":\"2025-05-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Small\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/smll.202503087\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smll.202503087","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

单分子DNA的捕获、线性化和成像是研究聚合物物理的生物物理学家和建立核酸分析方法(如光学作图)的工程师的广泛兴趣。在本研究中,单DNA分子在中性线性聚合物溶液中被轴向电场驱动通过微通道,并使用荧光显微镜研究其动力学。超过一定的阈值电场,单个DNA分子在每个分子的顶点被固定在通道壁上,并向与电场相反的方向拉伸。在移除电场后,固定的DNA分子在几秒钟内就会在顶点周围的布朗线圈上进行松弛。几十秒后,DNA被释放出来,自由扩散和电迁移。该方法使用易于制造的流体结构实现高通量单分子DNA的高质量成像。分析了捕获动力学、松弛动力学和顶点钉接可重复性所需的条件。假设中性线性(非交联)聚合物吸附到壁上并形成捕获DNA的支架。根据实验结果讨论了潜在的假设,以解释这种独特的捕获行为在非交联线性聚合物溶液中的潜在物理机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Vertex Pinning and Stretching of Single Molecule DNA in a Linear Polymer Solution

Vertex Pinning and Stretching of Single Molecule DNA in a Linear Polymer Solution

Trapping, linearization, and imaging of single-molecule DNA are of broad interest to both biophysicists who study polymer physics and engineers who build nucleic acid analysis methods such as optical mapping. In this study, single DNA molecules in a neutral linear polymer solution are driven with an axial electric field through microchannels, and their dynamics are studied using fluorescence microscopy. Above a certain threshold electric field, individual DNA molecules become pinned to the channel walls at a vertex on each molecule and are stretched in the direction opposite to electric field. Upon removal of the electric field, pinned DNA molecules undergo relaxation within a few seconds to a Brownian coil around the vertex. After tens of seconds, DNA is released and free to diffuse and electromigrate. The method enables high-quality imaging of single-molecule DNA with high throughput using simple-to-fabricate fluidic structures. The conditions required for trapping dynamics, relaxation dynamics, and the repeatability of vertex pinning are analyzed. It is hypothesized that the neutral linear (non-cross-linked) polymers adsorb to the wall and form scaffolds that trap DNA. Potential hypotheses are discussed based on the empirical findings to explain potential physical mechanism of such unique trapping behavior in a non-crosslinked linear polymer solution.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信