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DESCRIPTION (provided by applicant): A research program is proposed for achieving the goal of sequencing single molecules of DNA using transverse conductance probes located in a nanoscale channel. We believe, based upon first principle calculations, that the individual nucleotides making up a single strand polynucleotide can be distinguished by measuring the electrical tunneling current through the individual monomeric units perpendicular to the polymer backbone. The execution of this measurement strategy requires the development of at least two technological capabilities; the formation of nanometer scale fluidic channels for the localization of the polynucleotide and the formation of opposed conductance probes with these channels with nanoscale spacing and lateral extent. Nanoscale in the context of these experiments must truly be of molecular scale, in the range of about 1-2 nm. A combination of bottom-up and top-down nanofabrication strategies will be explored for the fabrication of devices that will allow demonstration of proof-of-principle concepts and further refinement to achieve single base-pair resolution. Our specific aims are listed below. * Develop top-down fabrication procedures for formation of fluidic nanochannels containing lateral dimensions of 2 nm or less. * Demonstration and characterization of ss DNA translocation through nanoscale channels. * Develop bottom-up fabrication strategies of nanoelectrodes with a lateral extent of less than 2 nm. Our discovery of unilateral epitaxial nanowire growth on (100) silicon will be developed to allow fabrication of these electrodes. * Experimentally characterize electron transport probability distribution functions and compare to theoretical simulations. * Determine experimental feasibility of distinguishing different types of nucleotides. Assignment error versus translocation rates will be experimentally determined and compared to simulations. * Single-base resolution by transverse electrode conductance measurements will be demonstrated.
期刊论文(22)
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DOI: 10.1021/jp111111u
发表时间: 2011-09-15
期刊: The journal of physical chemistry. B
影响因子: --
作者: [Cui S]
通讯作者: Cui S
DOI: 10.1021/jp909564d
发表时间: 2010-02-11
期刊: The journal of physical chemistry. B
影响因子: --
作者: [Cui S]
通讯作者: Cui S
DOI: 10.1021/nl103369g
发表时间: 2011-02-09
期刊: Nano letters
影响因子: 10.8
作者: [Menard LD, Ramsey JM]
通讯作者: Ramsey JM
DOI: 10.1103/physrevlett.103.128102
发表时间: 2009-09-18
期刊: Physical review letters
影响因子: 8.6
作者: [Zwolak M, Lagerqvist J, Di Ventra M]
通讯作者: Di Ventra M
14
    Nanofluidic Platforms for High Resolution Mapping of Genomic DNA
    Nanofluidic Platforms for High Resolution Mapping of Genomic DNA
    Nanofluidic Platforms for High Resolution Mapping of Genomic DNA
    Nanofluidic Platforms for High Resolution Mapping of Genomic DNA
    国内基金
    海外基金
    Handbook of the Mathematics of the Arts and Sciences的中文翻译
    • 批准号:
      12226504
    • 项目类别:
      数学天元基金项目
    • 资助金额:
      20.0万元
    • 批准年份:
      2022
    • 负责人:
      黄朝凌
    • 依托单位:
    ARTS在邻苯二甲酸(2-乙基己基)酯诱导的小鼠睾丸间质细胞凋亡中的作用及机理研究
    • 批准号:
      --
    • 项目类别:
      --
    • 资助金额:
      35万元
    • 批准年份:
      2020
    • 负责人:
      陈加祥
    • 依托单位:
    ARTS在邻苯二甲酸(2-乙基己基)酯诱导的小鼠睾丸间质细胞凋亡中的作用及机理研究
    • 批准号:
      82060278
    • 项目类别:
      地区科学基金项目
    • 资助金额:
      35.0万元
    • 批准年份:
      2020
    • 负责人:
      陈加祥
    • 依托单位:
    促进肿瘤凋亡的融合蛋白CPP-TRAIL-ARTS C27的制备及机制研究
    • 批准号:
      81372444
    • 项目类别:
      面上项目
    • 资助金额:
      70.0万元
    • 批准年份:
      2013
    • 负责人:
      易成
    • 依托单位: