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IRES: Vertically Integrated Team for Structural DNA NanoTech in Denmark

IRES: Vertically Integrated Team for Structural DNA NanoTech in Denmark
IRES:丹麦结构 DNA 纳米技术垂直整合团队
批准号:
1559077
负责人:
Thomas LaBean
金额:
$24.99万
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-05-01 至 2020-04-30

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中文摘要
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英文摘要
IRES: Vertically Integrated Team for Structural DNA NanoTech in Denmark This project sponsors a vertically integrated team (diverse members from education levels spanning high school through post-doctoral) of 5 or 6 participants per year from North Carolina for travel to Aarhus University in Denmark to pursue month-long research projects. Scientifically, the research project will advance the engineering of biological macromolecules (DNA and proteins) for formation of materials with their structures controlled on the nanometer length scale. The team leader will recruit participants from groups commonly underrepresented in science and engineering disciplines including minority and female students. This international research training experience will provide participants with unique opportunities to enlarge their scientific networks and to experience first-hand the benefits of cultural mixing. The project is important and deserves NSF funding, because it will develop molecular tools as well as scientific personnel capable of advancing nanoscience goals critical to the electronics and medical fields. US participants will benefit from significant scientific and social interactions with foreign students and faculty on-site in Denmark. The project will produce significant outcomes including cutting-edge research results and impactful research training experiences for participating American students. The senior investigators involved have received funding through the Danish National Research Foundation which primarily funds Danish students both in Denmark and on visits to the NCSU lab. IRES funding complements the Danish investment by allowing US students to participate in research at Aarhus. The project's scientific focus will be on the development of self-assembling DNA nanostructures and on their application toward nanofabrication of electronic, photonic, and biomedical devices. The NCSU team has used DNA as a building material to implement molecular computers, and to organize proteins and metallic nanoparticles with molecular-scale precision, while the Aarhus team is expert in DNA-guided chemistry for programmed synthesis of very large organic molecules. Developing ways to control matter on the nanoscale by exploiting the same construction principles used by biology (i.e. molecular recognition) holds great promise for diverse nanofabrication and biomedical applications. Engineered supramolecular complexes comprised of DNA, polypeptides, and inorganic nanomaterials provide the right length scale, range of physicochemical interactions, and complexity of shapes for interfacing effectively with biological structures. As such, DNA nanotechnology represents a perfect approach for creating custom diagnostic and ?smart? therapeutic agents for medical applications. Likewise, these same principles and materials are ideal for developing bionanofabrication procedures to compete with lithography for generation of electronic devices and circuits. Pursuit of biomimetic materials science, including molecular engineering for bottom-up assembly of complex nanostructures with diverse chemical, biological, photonic, or electronic functions, requires highly interdisciplinary teams. This cross-disciplinary work will therefore provide opportunities for very broad-based educational experiences to the participants. The cross-pollination provided by IRES funded international travel will lead to molecular materials engineering advances which could impact many fields of science and technology through applications in low-power nanoelectronics, programmable nanochemistry, novel biosensors, and smart therapeutics for biomedicine.
期刊论文(4)
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会议论文
DOI: 10.1088/1367-2630/18/11/115001
发表时间: 2016-11-17
期刊: NEW JOURNAL OF PHYSICS
影响因子: 3.3
作者: [Majikes, Jacob M., Nash, Jessica A., LaBean, Thomas H.]
通讯作者: LaBean, Thomas H.
DOI: 10.1021/acs.bioconjchem.7b00288
发表时间: 2017-07-01
期刊: BIOCONJUGATE CHEMISTRY
影响因子: 4.7
作者: [Majikes, Jacob M., Ferraz, Lucas C. C., LaBean, Thomas H.]
通讯作者: LaBean, Thomas H.
EAGER: SHF: Three-Dimensional Electronics Integration Facilitated by Molecular Assembly
  • 批准号:
    1748459
  • 项目类别:
    Standard Grant
  • 资助金额:
    $22.23万
  • 财政年份:
    2017
  • 负责人:
    Thomas LaBean
  • 依托单位:
Collaborative Research: BMAT: Adapting Cas9 Protein from CRISPR as a Structural Unit for Molecular Assembly
  • 批准号:
    1709010
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $21.0万
  • 财政年份:
    2017
  • 负责人:
    Thomas LaBean
  • 依托单位:
BME: DNA Origami for Investigating and Reprogramming Cell Signaling
  • 批准号:
    1603179
  • 项目类别:
    Standard Grant
  • 资助金额:
    $35.99万
  • 财政年份:
    2016
  • 负责人:
    Thomas LaBean
  • 依托单位:
Collaborative Research: Photonic and Electronic Devices Based on Self-Assembling DNA Templates
  • 批准号:
    1608847
  • 项目类别:
    Standard Grant
  • 资助金额:
    $21.01万
  • 财政年份:
    2016
  • 负责人:
    Thomas LaBean
  • 依托单位:
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