用荧光显微镜观察分离的单全基因组DNA上的oriC区域,用三联体形成的PNA探针

Y. Mori, H. Oana, H. Atomi, T. Imanaka, M. Washizu
{"title":"用荧光显微镜观察分离的单全基因组DNA上的oriC区域,用三联体形成的PNA探针","authors":"Y. Mori, H. Oana, H. Atomi, T. Imanaka, M. Washizu","doi":"10.1109/MHS.2007.4420830","DOIUrl":null,"url":null,"abstract":"This paper presents a methodology for analyzing intact Mb-size DNA which enables to obtain spatial information on the position of the specific sequence in single molecular level. We utilized the complex of Qdot-streptavidin conjugate and biotinylated PNA as a triplex forming fluorescent probe and tried to visualize a region of the origin site of chromosomal replication (oriC) on an intact genomic DNA of a hyperthermophilic archaeon, Thermococcus kodakaraensis KOD1. To improve the spatial resolution along the DNA, the DNA was dragged and elongated in the solution by the optical tweezers. PNA binding to homopurine sequence in oriC region of KOD1 was confirmed by the gel electrophoresis mobility shift assay and fluorescence optical mapping in single molecular level was demonstrated. However, we have not yet detected the oriC region specifically due to the difficulty of the complete elimination of the non-specific binding between Qdot-streptavidin conjugate and DNA.","PeriodicalId":161669,"journal":{"name":"2007 International Symposium on Micro-NanoMechatronics and Human Science","volume":"99 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2007-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Visualization of an oriC region on an isolated single whole-genome DNA with triplex forming PNA probe using fluorescence microscopy\",\"authors\":\"Y. Mori, H. Oana, H. Atomi, T. Imanaka, M. Washizu\",\"doi\":\"10.1109/MHS.2007.4420830\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This paper presents a methodology for analyzing intact Mb-size DNA which enables to obtain spatial information on the position of the specific sequence in single molecular level. We utilized the complex of Qdot-streptavidin conjugate and biotinylated PNA as a triplex forming fluorescent probe and tried to visualize a region of the origin site of chromosomal replication (oriC) on an intact genomic DNA of a hyperthermophilic archaeon, Thermococcus kodakaraensis KOD1. To improve the spatial resolution along the DNA, the DNA was dragged and elongated in the solution by the optical tweezers. PNA binding to homopurine sequence in oriC region of KOD1 was confirmed by the gel electrophoresis mobility shift assay and fluorescence optical mapping in single molecular level was demonstrated. However, we have not yet detected the oriC region specifically due to the difficulty of the complete elimination of the non-specific binding between Qdot-streptavidin conjugate and DNA.\",\"PeriodicalId\":161669,\"journal\":{\"name\":\"2007 International Symposium on Micro-NanoMechatronics and Human Science\",\"volume\":\"99 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2007-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2007 International Symposium on Micro-NanoMechatronics and Human Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/MHS.2007.4420830\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2007 International Symposium on Micro-NanoMechatronics and Human Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/MHS.2007.4420830","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

本文提出了一种分析完整的mb大小DNA的方法,该方法能够在单分子水平上获得特定序列位置的空间信息。我们利用qdot -链亲和素缀合物和生物素化的PNA作为三联体形成的荧光探针,并试图在嗜热古细菌柯达卡拉热球菌(Thermococcus kodakaraensis KOD1)的完整基因组DNA上可视化染色体复制起始位点(oriC)的区域。为了提高沿DNA的空间分辨率,用光学镊子在溶液中拖拽和拉长DNA。凝胶电泳迁移位移实验证实了PNA与KOD1 oriC区同嘌呤序列的结合,并证实了单分子水平的荧光光学定位。然而,由于难以完全消除Qdot-streptavidin偶联物与DNA之间的非特异性结合,我们尚未特异性检测到oriC区域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Visualization of an oriC region on an isolated single whole-genome DNA with triplex forming PNA probe using fluorescence microscopy
This paper presents a methodology for analyzing intact Mb-size DNA which enables to obtain spatial information on the position of the specific sequence in single molecular level. We utilized the complex of Qdot-streptavidin conjugate and biotinylated PNA as a triplex forming fluorescent probe and tried to visualize a region of the origin site of chromosomal replication (oriC) on an intact genomic DNA of a hyperthermophilic archaeon, Thermococcus kodakaraensis KOD1. To improve the spatial resolution along the DNA, the DNA was dragged and elongated in the solution by the optical tweezers. PNA binding to homopurine sequence in oriC region of KOD1 was confirmed by the gel electrophoresis mobility shift assay and fluorescence optical mapping in single molecular level was demonstrated. However, we have not yet detected the oriC region specifically due to the difficulty of the complete elimination of the non-specific binding between Qdot-streptavidin conjugate and DNA.
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
自引率
0.00%
发文量
0
×
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