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中文摘要
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描述(由申请人提供):一氧化氮(NO),一氧化碳(CO)和分子氧(O2)是哺乳动物中三种关键的气体信使。尽管在阐明这些分子的生物合成机制方面取得了重大进展,但对它们如何转导信号触发生理反应知之甚少。一氧化氮通过其血红素蛋白受体可溶性胍基环化酶(sGC)介导其生理作用。尽管经过三十年的研究,NO与sGC结合激活第二信使(cGMP)产生的结构基础尚不清楚。我们设计了创新的策略来深入了解这一过程。这包括我们发现了一个新的细菌NO传感器家族(SONO),它与sGC的传感器结构域具有显著的序列一致性。尽管SONO的信号在20亿年的进化过程中保持不变,但其功能与cGMP的生物合成无关。我们已经确定的sono -蛋白相互作用使我们能够提出一个具有挑衅性的假设,即NO传感器是一个混杂的分子开关,能够通过有限的结构变化触发功能无关的信号事件。为了验证这一假设,设计了四个具体目标:目标1。NO-和co -活化的SONO的结构是什么?目的2:人类sGC不依赖血红素和no信号的结构基础是什么?目标3:NO和活化剂结合是如何耦合到sGC催化的?目标4:SONO介导人类病原体趋化的分子机制是什么?提出的研究将为气体信使信号的机制提供新的见解。它还将为制定针对心血管疾病的治疗干预措施的合理战略铺平道路。公共卫生相关性:一氧化氮是一种由血管细胞产生的气体,它的几种功能之一是能将男性的性兴奋转化为勃起。这一提议旨在了解一氧化氮在健康和疾病状态下的作用。
英文摘要
DESCRIPTION (provided by applicant): Nitric oxide (NO), carbon monoxide (CO), and molecular oxygen (O2) are three key gaseous messengers in mammals. Although significant advances have been made in elucidating the mechanisms by which these molecules are biosynthesized, very little is known about how they transduce signals to trigger a physiological response. NO mediates its physiological actions via its heme protein receptor, soluble guanylyl cyclase (sGC). Despite three decades of research, the structural basis of how NO binding to sGC activates second messenger (cGMP) production is not understood. We have devised innovative strategies to gain insights into this process. This includes our discovery of a novel family of bacterial NO sensors (SONO) that share remarkable sequence identity with the sensor domain of sGC. Although the signal for SONO has remained unchanged during two billion years of evolution, its function is unrelated to cGMP biosynthesis. The SONO-protein interactions we have identified has allowed us to frame the provocative hypothesis that the NO sensor is a promiscuous molecular switch capable of triggering functionally unrelated signaling events via a limited set of structural changes. Four specific aims have been designed to test this hypothesis: Aim 1. What is the structure of NO- and CO-activated SONO? Aim 2: What are the structural bases of heme- and NO-independent signaling by human sGC? Aim 3: How is NO and activator binding coupled to sGC catalysis? Aim 4: What is the molecular mechanism by which SONO mediates chemotaxis in human pathogens? The proposed research will provide novel insights into mechanisms of gaseous messenger signaling. It will also pave the way for rational strategies aimed at developing therapeutic interventions for cardiovascular diseases. PUBLIC HEALTH RELEVANCE: Among the several functions of nitric oxide - a gas produced by the cells lining our blood vessels - is its ability to convert sexual excitement into erections in males. This proposal is aimed at understanding how nitric oxide works in healthy and disease states.
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STRUCTURAL BASIS OF CELLULAR SIGNALING
  • 批准号:
    8362114
  • 项目类别:
  • 资助金额:
    $0.34万
  • 财政年份:
    2011
  • 负责人:
    C S RAMAN
  • 依托单位:
STRUCTURAL BASIS OF CELLULAR SIGNALING
  • 批准号:
    8170021
  • 项目类别:
  • 资助金额:
    $0.45万
  • 财政年份:
    2010
  • 负责人:
    C S RAMAN
  • 依托单位:
STRUCTURAL BASIS OF CELLULAR SIGNALING
  • 批准号:
    7954313
  • 项目类别:
  • 资助金额:
    $0.79万
  • 财政年份:
    2009
  • 负责人:
    C S RAMAN
  • 依托单位:
Structural Biology of Gaseous Messenger Signaling
国内基金
海外基金
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
  • 批准号:
    81973577
  • 项目类别:
    面上项目
  • 资助金额:
    55.0万元
  • 批准年份:
    2019
  • 负责人:
    辛贵忠
  • 依托单位: