课题基金 / 基金详情

Center for Development of Biological Nanosensors (RMI)

Center for Development of Biological Nanosensors (RMI)
生物纳米传感器开发中心(RMI)
批准号:
6930922
负责人:
Douglas C. Eaton
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
项目状态:
已结题
起止时间:
2004-09-30 至 2005-07-31

项目摘要

项目成果

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中文摘要
翻译
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。虽然神经细胞和肌肉细胞等一些细胞可以通过电信号进行通信,但大多数细胞通过化学试剂进行通信,这些化学试剂会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)或生物体其他部分的细胞(外分泌剂)的活性 或激素)。正常的细胞功能通常取决于对这些药物释放量和时间的严格控制。许多病理事件涉及细胞之间化学通讯的破坏(最明显的是中枢神经系统、心脏、肺和肾脏)。由于这些化学信使的重要性,大量的研究工作致力于确定细胞释放的特性。 然而,由于这些方法大多数是间接的或空间或时间分辨率较低,因此关于此类药物的释放仍然存在许多未解答的问题。本计划提出了一种创新的、多学科的方法来研究分子水平上的细胞通讯过程。该提案利用了两个小组的综合专业知识。细胞与分子信号传导中心 (CCMS) 将采取行动 组织埃默里校区的生物专业知识,而应用传感器实验室(ASL)将作为佐治亚理工学院校园的焦点,开发研究生物问题所需的纳米技术。 CCMS 和 ASL 已经建立了持续的研究计划和合作资助,利用纳米技术来检查肺和肾细胞系统中的生物活性分子。该跨学科计划将重点关注集成扫描纳米探针传感系统的应用。扫描探针显微镜技术为获取高空间分辨率的化学、形貌和光学信息提供了强大的手段。原子力显微镜 (AFM)、扫描近场光学显微镜 (SNOM) 和扫描电化学显微镜 (SECM) 等每种技术都旨在提供特定类型的生物数据。 SECM 提供有关细胞表面生物分子活性的信息。概念验证实验已经确立了此类方法的实用性,可以以高时间和空间分辨率测量细胞表面的旁分泌剂(如 ATP 和活性氧),这是复杂生物系统原位研究所需的信息。这些知识可能有助于更好地理解与细胞通讯过程相关的疾病,如糖尿病、肺囊性纤维化和多囊肾疾病的治疗,并制定新的治疗策略。
英文摘要
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.
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Institutional Research and Academic Career Development
  • 批准号:
    7895127
  • 项目类别:
  • 资助金额:
    $30.11万
  • 财政年份:
    2009
  • 负责人:
    Douglas C. Eaton
  • 依托单位:
REGULATION OF SODIUM IN TIGHT EPITHELIA
  • 批准号:
    7990026
  • 项目类别:
  • 资助金额:
    $10.0万
  • 财政年份:
    2009
  • 负责人:
    Douglas C. Eaton
  • 依托单位:
Cellular Signaling and Kidney Function
  • 批准号:
    7850092
  • 项目类别:
  • 资助金额:
    $2.98万
  • 财政年份:
    2009
  • 负责人:
    Douglas C. Eaton
  • 依托单位:
Cellular Signaling and Kidney Function
  • 批准号:
    7499285
  • 项目类别:
  • 资助金额:
    $8.81万
  • 财政年份:
    2007
  • 负责人:
    Douglas C. Eaton
  • 依托单位:
海外基金