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Development of Biosensor Comprising DNA as Affinity Ligand

Development of Biosensor Comprising DNA as Affinity Ligand
以DNA为亲和配体的生物传感器的研制
批准号:
05558114
负责人:
MAEDA Mizuo
金额:
$3.26万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Developmental Scientific Research (B)
财政年份:
1993
资助国家:
日本
项目状态:
已结题
起止时间:
1993 至 1994

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中文摘要
翻译
生物传感器等传感技术中的分子识别功能通常由酶和抗体等蛋白质提供。另一方面,DNA也是生物亲和反应中重要的宿主分子。本研究开发了一种新的金属电极固定双螺旋DNA的修饰化学方法。研究了该电极在生物亲和传感领域的应用前景。DNA双链通过化学吸附固定在金电极上,即与含硫部分配位。用dna修饰电极对亚铁氰化物/铁氰化物氧化还原对进行循环伏安。当加入著名的抗疟疾药物奎纳克里时,峰值电流随着药物浓度的增加而增加。峰值电流在10^<-7>-5 × 10^<-7 >m范围内与醌浓度基本呈线性关系,超过8x^<-7 >m时达到饱和。阳离子药物与固定化DNA的结合应减少多阴离子DNA与阴离子氧化还原偶离子之间的静电斥力,从而使电流强度增强。此外,发现dna修饰电极可用于“基因传感器”。该传感器不仅可用于DNA的测量,还可用于评价DNA与一系列DNA结合药物之间的相互作用。
英文摘要
A molecular recognition function employed in sensing techniques such as biosensors is usually provided by proteins including enzymes and antibodies. On the other hand, DNA is also an important host molecule in biological affinity reactions. We have developed in this study a new modification chemistry for immobilizing double-helical DNA on metal electrode. Some possible application of the electrode for bioaffinity-based sensing has been studied.DNA double strands were immobilized on a Au electrode via chemisorption, i.e., a co-ordination to Au with a sulfur-containing moiety. Cyclic voltammograms of ferrocyanide/ferricyanide redox couple were taken with the DNA-modified electrode. When adding quinacrine, the well-known antimalarial drug, the peak currents increased with increasing concentration of the drug. The peak current showed almost a linear relationship with the concentration of quinacrine in the range of 10^<-7>-5x10^<-7>M and then saturated beyond the concentration of 8x^<-7>M.The binding of the cationic drug to the immobilized DNA should reduce the electrostatic repulsion between the polyanionic DNA and the anionic redox couple ions, resulting in the enhancement of the current intensity.In addition, the DNA-modified electrode was found to be useful for"gene sensor". The sensor comprising DNA as a receptive component can be used for not only the measurement of DNA but also the evaluation of the interaction between DNA and a family of DNA-binding drugs.
期刊论文(18)
专著(0)
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会议论文
Mizuo Maeda, Chitoshi Nishimura, Daisuke Umeno, Makoto Takagi: ""A Psoralen-Containing Vinyl Monomer for Copnjugation of Double-Helical DNA with Vinyl Polymers"" Bioconjugate Chem. 5. 527-531 (1994)
Mizuo Maeda、Chitoshi Nishimura、Daisuke Umeno、Makoto Takagi:“用于双螺旋 DNA 与乙烯基聚合物共轭的含补骨脂素乙烯基单体”Bioconjugate Chem。
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通讯作者:
Mizuo Maeda, Chitoshi Nishimura, Akiko Inenaga, Makoto Takagi: ""Modification of DNA with Poly (N-Isopropylacrylamide) for Thermally Induced Affinity Separation."" Reactive Polym. 21. 27-35 (1993)
Mizuo Maeda、Chitoshi Nishimura、Akiko Inenaga、Makoto Takagi:“用聚(N-异丙基丙烯酰胺)修饰 DNA 以实现热诱导亲和分离。”反应性聚合物。
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Mizuo Maeda: "Semi-Synthetic macromalecular Conjugates for Biomimetic Sensors" ACS Symposium Series. 556. 238-251 (1994)
Mizuo Maeda:“用于仿生传感器的半合成大分子缀合物”ACS 研讨会系列。
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通讯作者:
Mizuo Maeda: "A Psoralen-Containing Vinyl Monomer for Conjugation of Double-Helical DNA" Bioconjugate Chem.5. 527-531 (1994)
Mizuo Maeda:“用于缀合双螺旋 DNA 的含补骨脂素的乙烯基单体”Bioconjugate Chem.5。
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共 16 条
    Creation of Biomaterials Endowed with Unique Properties of DNA Soft-Interfaces
    Highly quantitative gene analysis based on affinity capillary electrophoresis using DNA conjugates
    Molecular Design of DNA Conjugate and its Applications to Biosensing
    • 批准号:
      15200039
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $31.45万
    • 财政年份:
      2003
    • 负责人:
      MAEDA Mizuo
    • 依托单位:
    Separation of Oligodeoxyribonucleotides Having Single-base Mutation by Affinity Capillary Electrophoresis Using a DNA- polyacrylamide Conjugate
    • 批准号:
      12555237
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $6.08万
    • 财政年份:
      2000
    • 负责人:
      MAEDA Mizuo
    • 依托单位:
    国内基金
    海外基金
    NAD+/NADH Biosensor “智能”调控好氧/厌氧耦合供给NADH产氢研究
    • 批准号:
      31970038
    • 项目类别:
      面上项目
    • 资助金额:
      58.0万元
    • 批准年份:
      2019
    • 负责人:
      赵洪新
    • 依托单位: