Center for Development of Biological Nanosensors (RMI)

生物纳米传感器开发中心(RMI)

基本信息

  • 批准号:
    6930922
  • 负责人:
  • 金额:
    $ 7.65万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2004
  • 资助国家:
    美国
  • 起止时间:
    2004-09-30 至 2005-07-31
  • 项目状态:
    已结题

项目摘要

Secretion of transmitters, hormones, and other biologically active molecules depends upon a complex sequence of cellular events. Although some cells like nerve and muscle cells can communicate through electrical signals, most cells communicate through chemical agents that alter the activity of the cells from which they are released (known as autocrine agents), nearby cells (paracrine agents or transmitters), or cells in other parts of the organism (exocrine agents or hormones). Normal cellular function usually depends upon the very tight control of the amount and timing of the release of these agents. Many pathological events involve disruption of chemical communication between cells (most notably in the central nervous system, heart, lungs, and kidneys). Because of the importance of these chemical messengers, an enormous research effort has been directed to determining the properties of release from cells. However, because most of these methods are indirect or have low spatial or temporal resolution, there are still many unanswered questions concerning the release of such agents. The present program proposes an innovative, multidisciplinary approach to the investigation of cell communication processes at the molecular level. This proposal takes advantage of the combined expertise of two groups. The Center for Cell & Molecular Signaling (CCMS) will act to organize the biological expertise on the Emory campus while the Applied Sensors Laboratory (ASL) will act as the focal point on the Georgia Tech campus for development of the nanotechnology needed to study biological problems. CCMS and ASL already have established ongoing research programs and collaborative grants using nanotechnology to examine biologically active molecules in lung and renal cell systems. The interdisciplinary Program will focus on the application of integrated scanning nanoprobe sensing systems. Scanning probe microscopy techniques provide powerful means for obtaining chemical, topographical and optical information with high spatial resolution. Each technique -atomic force microscopy (AFM), scanning near field optical microscopy (SNOM) and scanning electrochemical microscopy (SECM) - is designed to provide a specific kind of biological data. SECM provides information on the activity of biological molecules at cell surfaces. Proof of concept experiments have already established the utility of such methods to measure paracrine agents like ATP and reactive oxygen species at cell surfaces with high temporal and spatial resolution, information required for in situ investigations of complex biological systems. This knowledge may lead to better understanding and new strategies for treatment of disorders specifically related to cell communication crocesses like diabetes, cystic fibrosis in the lung, and polycystic kidney disease.
递质、激素和其他生物活性分子的分泌取决于一系列复杂的细胞事件。虽然有些细胞,如神经和肌肉细胞可以通过电信号进行交流,但大多数细胞通过化学物质进行交流,这些化学物质可以改变释放它们的细胞(称为自分泌剂)、附近细胞(旁分泌剂或递质)或生物体其他部位的细胞(外分泌剂)的活动

项目成果

期刊论文数量(0)
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Douglas C. Eaton其他文献

Regulation of the epithelial sodium channel by phosphatidylinositides: experiments, implications, and speculations
Acid pH and weak acids induce Na−Cl contransport in the rabbit urinary bladder
酸性 pH 值和弱酸诱导兔膀胱中的 Na−Cl 转运
  • DOI:
  • 发表时间:
    2005
  • 期刊:
  • 影响因子:
    2.4
  • 作者:
    M. S. Ifshin;Karen E. Johnson;Douglas C. Eaton
  • 通讯作者:
    Douglas C. Eaton
Polymerase delta-interacting protein 2 mediates brain vascular permeability by regulating ROS-mediated ZO-1 phosphorylation and localization at the interendothelial border
  • DOI:
    10.1186/s12964-024-01982-3
  • 发表时间:
    2025-01-07
  • 期刊:
  • 影响因子:
    8.900
  • 作者:
    Keke Wang;Hongyan Qu;Ruinan Hu;Bernard Lassègue;Douglas C. Eaton;Chang Song;Jianjun Mu;Kathy K. Griendling;Marina S. Hernandes
  • 通讯作者:
    Marina S. Hernandes
Dampened GM-CSF signaling and impaired innate immune function in alveolar macrophages in the alcoholic lung
  • DOI:
    10.1016/j.alcohol.2006.09.017
  • 发表时间:
    2006-06-01
  • 期刊:
  • 影响因子:
  • 作者:
    David M. Guidot;Pratibha C. Joshi;Lou Ann Brown;Douglas C. Eaton;Jesse Roman
  • 通讯作者:
    Jesse Roman
The mechanism of Na+ transport by rabbit urinary bladder
  • DOI:
    10.1007/bf01869690
  • 发表时间:
    1976-12-01
  • 期刊:
  • 影响因子:
    2.900
  • 作者:
    Simon A. Lewis;Douglas C. Eaton;Jared M. Diamond
  • 通讯作者:
    Jared M. Diamond

Douglas C. Eaton的其他文献

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{{ truncateString('Douglas C. Eaton', 18)}}的其他基金

Institutional Research and Academic Career Development
机构研究和学术职业发展
  • 批准号:
    7895127
  • 财政年份:
    2009
  • 资助金额:
    $ 7.65万
  • 项目类别:
REGULATION OF SODIUM IN TIGHT EPITHELIA
紧密上皮细胞中钠的调节
  • 批准号:
    7990026
  • 财政年份:
    2009
  • 资助金额:
    $ 7.65万
  • 项目类别:
Cellular Signaling and Kidney Function
细胞信号传导和肾功能
  • 批准号:
    7850092
  • 财政年份:
    2009
  • 资助金额:
    $ 7.65万
  • 项目类别:
Cellular Signaling and Kidney Function
细胞信号传导和肾功能
  • 批准号:
    7499285
  • 财政年份:
    2007
  • 资助金额:
    $ 7.65万
  • 项目类别:
ENaC Assembly, Trafficking, and Degradation
ENaC 组装、贩运和降解
  • 批准号:
    7471477
  • 财政年份:
    2007
  • 资助金额:
    $ 7.65万
  • 项目类别:
Cellular Signaling and Kidney Function
细胞信号传导和肾功能
  • 批准号:
    6860925
  • 财政年份:
    2004
  • 资助金额:
    $ 7.65万
  • 项目类别:
Cellular Signaling and Kidney Function
细胞信号传导和肾功能
  • 批准号:
    7098737
  • 财政年份:
    2004
  • 资助金额:
    $ 7.65万
  • 项目类别:
Cellular Signaling and Kidney Function
细胞信号传导和肾功能
  • 批准号:
    7471483
  • 财政年份:
    2004
  • 资助金额:
    $ 7.65万
  • 项目类别:
Cellular Signaling and Kidney Function
细胞信号传导和肾功能
  • 批准号:
    6951813
  • 财政年份:
    2004
  • 资助金额:
    $ 7.65万
  • 项目类别:
ENaC Assembly, Trafficking, and Degradation
ENaC 组装、贩运和降解
  • 批准号:
    6866956
  • 财政年份:
    2004
  • 资助金额:
    $ 7.65万
  • 项目类别:

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细胞粘附在生物信号转导中的作用
  • 批准号:
    6238317
  • 财政年份:
    1997
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