发卡型万能传导在基于核酸分子线路的基因诊断中的应用和性能优化
详细信息    查看全文 | 推荐本文 |
  • 英文篇名:Adaption and Optimization of Universal Hairpin Transduction in Gene Diagnostics Based on Nucleic Acid Circuits
  • 作者:唐艺丹 ; 刘一辰 ; 吕佰阳 ; 郭路路 ; 李冰凌
  • 英文作者:TANG Yi-Dan;LIU Yi-Chen;LYU Bai-Yang;GUO Lu-Lu;LI Bing-Ling;State Key Laboratory of Electroanalytical Chemistry,Changchun Institute of Applied Chemistry,Chinese Academy of Sciences;University of Chinese Academy of Sciences;
  • 关键词:等温扩增 ; 万能中转 ; 发卡型中转探针 ; 核酸分子线路 ; 催化发卡型结构自组装 ; 荧光 ; 电化学
  • 英文关键词:Isothermal amplification;;Universal transduction;;Hairpin transducer;;Nucleic acid circuit;;Catalytic hairpin assembly;;Fluorescence;;Electrochemistry
  • 中文刊名:FXHX
  • 英文刊名:Chinese Journal of Analytical Chemistry
  • 机构:中国科学院长春应用化学研究所,电分析化学国家重点实验室;中国科学院大学;
  • 出版日期:2018-06-08
  • 出版单位:分析化学
  • 年:2018
  • 期:v.46
  • 基金:国家自然科学基金项目(No.21505129);; 吉林省自然科学基金项目(No.20160101296JC);; 王宽诚率先人才计划-卢嘉锡国际团队项目资助~~
  • 语种:中文;
  • 页:FXHX201806008
  • 页数:10
  • CN:06
  • ISSN:22-1125/O6
  • 分类号:72-81
摘要
核酸等温扩增技术作为核酸体外扩增技术,其反应过程始终维持在恒定温度下。与聚合酶链反应相比,核酸等温扩增反应具有优异的便携型,因而被视为最有望实现基因快检甚至即时快检的体外基因扩增方法。然而,由于反应过程中假阳性扩增频发、反应后对产物的检测方法缺乏特异性和灵敏度等缺点,限制了其在实际分析检测中的应用。通过构建发卡型结构万能中转探针,成功地将恒温扩增产物转到一套性能良好的已知核酸分子线路上;借助核酸分子线路的百倍放大性能和序列特异性,实现对上游基因序列信息的精准识别和放大信号输出。针对不同的待测序列,仅需改变发卡型中转探针的序列,即可实现对不同序列目标物的检测。基于中转探针的重要性,本研究对中转探针的设计原理和方法进行了重点阐述,提出并验证了一套行之有效的普适性设计规律,确保中转探针良好的中转效率(信噪比)。利用这一规律获得的中转探针,与核酸分子线路偶联,可成功为低至近单分子(20个拷贝)的模型基因提供显著荧光和电化学信号输出。
        Isothermal nucleic acid amplifications,as powerful as polymerase chain reaction but functioning at a constant temperature, are considered to be very promising technique in achieving point-of-care gene diagnostics. However,until now,their practical applications are still seriously lagged by the bad reliability resulting from the problems such as false positive amplification and low signal amplitude. In this work,a universal transduction method in which any sequence( including loop-mediated isothermal amplification products) could be transduced via a hairpin transducer into a catalyst of a well-engineered circuit( catalytic hairpin assembly,CHA) was established. Because CHA circuit could amplify tens to hundreds fold with especially high sequence specificity,it could provide both accuracy and high amplitude for sequence detection.And for a new targeting sequence,the only sequence needed to be changed was the hairpin transducer. Due to the importance of the transducer,we provided and verified a universal designing rule-set to guarantee the transducing efficiency( signal to background ratio) of the transducer. Transducers designed following this rule set were then proved to be very efficient in detecting pathogen gene targets. As less as near single molecule( 20 copies) of pathogen genes could be detected with significant fluorescent and electrochemical signals.
引文
1 Liu D Y,Daubendiek S L,Zillman M A,Ryan K,Kool E T.J.Am.Chem.Soc.,1996,118(7):1587-1594
    2 Guatelli J C,Whitfield K M,Kwoh D Y,Barringer K J,Richman D D,Gingeras T R.Proc.Natl.Acad.Sci.USA,1990,87(5):1874-1878
    3 Compton J.Nature,1991,350(6313):91-92
    4 Walker G T,Fraiser M S,Schram J L,Little M C,Nadeau J G,Malinowski D P.Nucleic Acids Res.,1992,20(7):1691-1696
    5 Notomi T,Okayama H,Masubuchi H,Yonekawa T,Watanabe K,Amino N,Hase T.Nucleic Acids Res.,2000,28(12):e63
    6 Vincent M,Xu Y,Kong H M.EMBO Rep.,2004,5(8):795-800
    7 Piepenburg O,Williams C H,Stemple D L,Armes N A.PLOS Biol.,2006,4(7):e204
    8 Craw P,Balachandran W.Lab Chip,2012,12(14):2469-2486
    9 Gill P,Ghaemi A.Nucleosides Nucleotides Nucleic Acids,2008,27(3):224-243
    10 Zhang X Z,Lowe S B,Gooding J J.Biosens.Bioelectron.,2014,61:491-499
    11 Li J,Macdonald J.Biosens.Bioelectron.,2015,64:196-211
    12 Li B L,Chen X,Ellington A D.Anal.Chem.,2012,84(19):8371-8377
    13 Zhao Y X,Chen F,Li Q,Wang L H,Fan C H.Chem.Rev.,2015,115(22):12491-12545
    14 Stojanovic M N,Stefanovic D,Rudchenko S.Acc.Chem.Res.,2014,47(6):1845-1852
    15 Wang F A,Lu C H,Willner I.Chem.Rev.,2014,114(5):2881-2941
    16 Jung C,Ellington A D.Acc.Chem.Res.,2014,47(6):1825-1835
    17 Bi S,Yue S Z,Zhang S S.Chem.Soc.Rev.,2017,46(14):4281-4298
    18 Qu X M,Zhu D,Yao G B,Su S,Chao J,Liu H J,Zuo X L,Wang L H,Shi J Y,Wang L H,Huang W,Pei H,Fan C H.Angew.Chem.Int.Edit.,2017,56(7):1855-1858
    19 Dirks R M,Pierce N A.Proc.Natl.Acad.Sci.USA,2004,101(43):15275-15278
    20 Choi H M T,Chang J Y,Trinh L A,Padilla J E,Fraser S E,Pierce N A.Nat.Biotechnol.,2010,28(11):1208-1212
    21 Zhang D Y,Turberfield A J,Yurke B,Winfree E.Science,2007,318(5853):1121-1125
    22 Yin P,Choi H M T,Calvert C R,Pierce N A.Nature,2008,451(7176):318-322
    23 Li B L,Ellington A D,Chen X.Nucleic Acids Res.,2011,39(16):e110
    24 Wu Z K,Fan H H,Satyavolu N S R,Wang W J,Lake R,Jiang J H,Lu Y.Angew.Chem.Int.Edit.,2017,56(30):8721-8725
    25 Li F,Zhang H Q,Wang Z X,Li X K,Li X F,Le X C.J.Am.Chem.Soc.,2013,135(7):2443-2446
    26 Wu C C,Cansiz S,Zhang L Q,Teng I T,Qiu L P,Li J,Liu Y,Zhou C S,Hu R,Zhang T,Cui C,Cui L,Tan W H.J.Am.Chem.Soc.,2015,137(15):4900-4903
    27 Ma C P,Wang W S,Li Z X,Cao J J,Wang Q Y.Anal.Biochem.,2012,429(2):99-102
    28 Jiang Y,Li B L,Milligan J N,Bhadra S,Ellington A D.J.Am.Chem.Soc.,2013,135(20):7430-7433
    29 Yang Z L,Liu Y C,Lu W,Yuan Q P,Wang W,Pu Q S,Yao B.Talanta,2016,152:301-307
    30 Qu X M,Wang S P,Ge Z L,Wang J B,Yao G B,Li J,Zuo X L,Shi J Y,Song S P,Wang L H,Li L,Pei H,Fan C H.J.Am.Chem.Soc.,2017,139(30):10176-10179
    31 Tang Y D,Lu B Y,Zhu Z T,Li B L.Chem.Sci.,2018,9(3):760-769
    32 Li B L,Jiang Y,Chen X,Ellington A D.J.Am.Chem.Soc.,2012,134(34):13918-13921
    33 Tang Y D,Zhu Z T,Lu B Y,Li B L.Chem.Commun.,2016,52(88):13043-13046

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700