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HIV-1电化学活性-非活性开关分子信标的构建及验证
引用本文:李博,顾大勇,司徒博,李政良,颜晓慧,刘芹兰,郑磊,王前. HIV-1电化学活性-非活性开关分子信标的构建及验证[J]. 检验医学, 2012, 27(5): 408-411
作者姓名:李博  顾大勇  司徒博  李政良  颜晓慧  刘芹兰  郑磊  王前
作者单位:1. 南方医科大学南方医院检验医学科(系)临床快速检验实验室,广东广州,510515
2. 深圳国际旅行卫生保健中心,广东深圳,518033
3. 南方医科大学南方医院临床实验研究中心,广东广州,510515
基金项目:广东省科技计划国际合作项目,广东省科技计划项目,广东省自然科学基金,国家质检总局科技计划项目
摘    要:目的构建人类免疫缺陷病毒1型(HIV-1)电化学活性-非活性开关分子信标(CAs-MB)并验证其结构及功能。方法合成并纯化针对HIV-1 gag基因保守区序列的CAs-MB,用傅里叶变换红外光谱(FT-IR)和循环伏安法(CV)验证其结构,用差分脉冲伏安法(DPV)信号强度评价CAs-MB的识别功能。结果胭脂红酸(CA)单体与CAs-MB FT-IR图的变化证明CA已标记于MB末端,CV图证明CAs-MB电化学活性ON和OFF状态的存在。DPV结果证实其能够在电化学平台上实现对目标序列的特异性识别,且能够区分一个碱基的差异。结论 CAs-MB作为HIV-1 gag基因的特异性识别元件有望用于构建新型HIV-1电化学基因传感器。

关 键 词:人类免疫缺陷病毒1型  分子信标  电化学基因传感器

The construction and confirmation of HIV-1 electrochemically active-inactive switching molecular beacon
LI Bo , GU Dayong , SITU Bo , LI Zhengliang , YAN Xiaohui , LIU Qinlan , ZHENG Lei , WANG Qian. The construction and confirmation of HIV-1 electrochemically active-inactive switching molecular beacon[J]. Laboratory Medicine, 2012, 27(5): 408-411
Authors:LI Bo    GU Dayong    SITU Bo    LI Zhengliang    YAN Xiaohui    LIU Qinlan    ZHENG Lei    WANG Qian
Affiliation:1. Laboratory of Point-of-care Testing, Clinical Laboratory Center, Nanfang Hospital, Southern Medical University, Gnangdong Guangzhou 510515, China ;2. Shenzhen International Travel Health Care Center, Gnangdong Shenzhen 518033, China ;3. Research Center of Clinical Medicine, Nanfang Hospital, Southern Medical University, Guangdong Guangzhou 510515, China)
Abstract:Objective To construct human immunodeficiency virus-1 (HIV-1) electrochemically active-inactive switching molecular beacon (CAs-MB) and confirm its structure and function. Methods CAs-MB targeted conserved region of HIV-1 gag gene was prepared and purified. The structure was confirmed by Fourier transform-infrared spectroscopy (FF-IR) and cyclic voltmnmetry (CV), while its function of recognizing targets was evaluated by differential pulse vohammetry (DPV). Results The variations of FF-IR spectra of free carminicacid (CA) and CAs-MB indicated that CA had covalently linked onto the ends of MB. The results of CV proved that both ON and OFF statuses of CAs-MB were existing. DPV results illustrated that CAs-MB was effective in signaling the presence of complementary target and discriminating targets in electrochemical gene biosensor that differ by a single nucleotide. Conclusions CAs-MB opens a new detective technique and can be expanded to electrochemical gene biosensor to perform HIV-1 gag gene specificity detection.
Keywords:Human immunodeficiency virus-l  Molecular beacon  Electrochemical gene biosensor
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