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四色荧光标记二硫键可逆终端的合成及在DNA合成测序中的应用
引用本文:汤道年,江敏,李小卫,康亚妮,伍新燕,龚兵,邵志峰,赵小东,沈玉梅.四色荧光标记二硫键可逆终端的合成及在DNA合成测序中的应用[J].高等学校化学学报,2014,35(11):2346-2352.
作者姓名:汤道年  江敏  李小卫  康亚妮  伍新燕  龚兵  邵志峰  赵小东  沈玉梅
作者单位:1. 上海交通大学系统生物医学研究院, 系统生物医学教育部重点实验室,2. 生物医学工程学院, Bio-ID研究中心, 上海 2002403. 华东理工大学化学与分子工程学院, 先进材料重点实验室和精细化工研究所, 上海 2002374. 北京师范大学化学学院, 北京 1008755. 布法罗纽约州立大学化学系, 纽约 14260
基金项目:国家自然科学基金,科技重大专项“重大新药创制”项目
摘    要:分别以5-碘-2'-脱氧尿苷、 5-碘-2'-脱氧胞苷、 7-去氮-7-碘-2'-脱氧腺苷及7-去氮-7-碘-2'-脱氧鸟苷为原料, 以二硫键为可裂解连接单元, 通过多步反应合成了四色荧光标记不同碱基的脱氧核糖核苷酸; 研究了该类荧光标记核苷酸作为可逆终端在DNA合成测序中的应用. 所得产物结构经1H NMR, 31P NMR及HRMS表征, 并对其进行了DNA高通量测序的测试. 结果表明, 该类荧光标记核苷酸作为DNA合成测序的可逆终端能够满足高通量测序的生化反应要求, 具有较好的应用前景.

关 键 词:DNA合成测序  可逆终端  可裂解连接单元  四色荧光标记  
收稿时间:2014-03-24

Synthesis and Application of Four Fluorescence Labeled Nucleotides Through Disulfide as Reversible Terminators in DNA Sequencing by Synthesis
TANG Daonian,JIANG Min,LI Xiaowei,KANG Yani,WU Xinyan,GONG Bing,SHAO Zhifeng,ZHAO Xiaodong,SHEN Yumei.Synthesis and Application of Four Fluorescence Labeled Nucleotides Through Disulfide as Reversible Terminators in DNA Sequencing by Synthesis[J].Chemical Research In Chinese Universities,2014,35(11):2346-2352.
Authors:TANG Daonian  JIANG Min  LI Xiaowei  KANG Yani  WU Xinyan  GONG Bing  SHAO Zhifeng  ZHAO Xiaodong  SHEN Yumei
Institution:TANG Daonian;JIANG Min;LI Xiaowei;KANG Yani;WU Xinyan;GONG Bing;SHAO Zhifeng;ZHAO Xiaodong;SHEN Yumei;Shanghai Center for Systems Biomedicine,Key Laboratory of Systems Biomedicine,Ministry of Education,Shanghai Jiao Tong University;Key Laboratory for Advanced Materials and Institute of Fine Chemicals,School of Chemistry & Molecular Engineering,East China University of Science and Technology;School of Biomedical Engineering,Bio-ID Center,Shanghai Jiao Tong University;College of Chemistry,Beijing Normal University;Department of Chemistry,University at Buffalo,the State University of New York;
Abstract:DNA sequencing is one of the important means of biological research. The development of accurate and high-throughput DNA-sequencing methods has a strong impact on biomedical research. Sequencing by synthesis(SBS) approaches is one of the most important techniques of DNA sequencing. A series of SBS methods have been investigated and implemented. In SBS methods, the principal thing is to synthesize four fluorescently labelled cyclic reversible terminators as the sequencing reagents. These cyclic reversible terminators need to connect the fluorescein through a cleavable linker. In chemical biology, disulfide bridges, which are known to be efficiently and rapidly cleaved by mild reducing agents, have been used in a wide range of applications including drug delivery, functional and structural proteomics, DNA and tumor imaging. The disulfide-based cleavable linker is commonly used due to its rapid cleavage and straightforward synthesis. In this work, starting from 5-iodo-2'-deoxyuridine, 5-iodo-2'-deoxycyridine, 7-deazo-7-iodo-2'-deoxyadenosine and 7-deazo-7-iodo-2'-deoxyguanosine, four kinds of fluorescence labelled necleotides with four different bases through disulfide were synthesized and characterized. The synthesized fluorescence labelled nucleotides can be recognized and accepted by an identified DNA polymerase, incorporated faithfully into DNA strand, followed by cleaved completely by DTT within 1 min. These results demonstrate that the fluorescence labelled nucleotides have potential value as reversible terminators in DNA sequencing by synthesis.
Keywords:DNA sequencing by synthesis  Reversible terminator  Cleavable linker  Four fluorescence labelled nucleotide
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