Structural Biology of Gaseous Messenger Signaling

气体信使信号的结构生物学

基本信息

  • 批准号:
    8134305
  • 负责人:
  • 金额:
    $ 28.83万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2008
  • 资助国家:
    美国
  • 起止时间:
    2008-09-05 至 2012-07-31
  • 项目状态:
    已结题

项目摘要

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.
描述(由申请人提供):一氧化氮(NO)、一氧化碳(CO)和分子氧(O2)是哺乳动物中的三种关键气体信使。虽然在阐明这些分子生物合成的机制方面取得了重大进展,但对它们如何传递信号以触发生理反应知之甚少。NO通过其血红素蛋白受体可溶性鸟苷酸环化酶(sGC)介导其生理作用。尽管经过了三十年的研究,但NO与sGC结合如何激活第二信使(cGMP)产生的结构基础尚不清楚。我们制定了创新战略,以深入了解这一过程。这包括我们发现了一个新的细菌NO传感器家族(SONO),该家族与sGC的传感器结构域具有显着的序列同一性。虽然SONO的信号在20亿年的进化中保持不变,但其功能与cGMP生物合成无关。我们已经确定的SONO-蛋白质相互作用使我们能够构建一个挑衅性的假设,即NO传感器是一个混杂的分子开关,能够通过一组有限的结构变化触发功能无关的信号传导事件。为了检验这一假设,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sGC的血红素和NO非依赖性信号传导的结构基础是什么?目的3:NO和激活剂结合如何与sGC催化偶联?目的4:SONO介导人类病原体趋化性的分子机制是什么?这项研究将为气体信使信号传导机制提供新的见解。它还将为旨在制定心血管疾病治疗干预措施的合理战略铺平道路。公共卫生关系:一氧化氮是一种由血管细胞产生的气体,它有多种功能,其中之一就是能够将男性的性兴奋转化为勃起。该提案旨在了解一氧化氮如何在健康和疾病状态下发挥作用。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

C S RAMAN其他文献

C S RAMAN的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('C S RAMAN', 18)}}的其他基金

STRUCTURAL BASIS OF CELLULAR SIGNALING
细胞信号传导的结构基础
  • 批准号:
    8362114
  • 财政年份:
    2011
  • 资助金额:
    $ 28.83万
  • 项目类别:
STRUCTURAL BASIS OF CELLULAR SIGNALING
细胞信号传导的结构基础
  • 批准号:
    8170021
  • 财政年份:
    2010
  • 资助金额:
    $ 28.83万
  • 项目类别:
STRUCTURAL BASIS OF CELLULAR SIGNALING
细胞信号传导的结构基础
  • 批准号:
    7954313
  • 财政年份:
    2009
  • 资助金额:
    $ 28.83万
  • 项目类别:
Structural Biology of Gaseous Messenger Signaling
气体信使信号的结构生物学
  • 批准号:
    8060227
  • 财政年份:
    2008
  • 资助金额:
    $ 28.83万
  • 项目类别:
Structural Biology of Gaseous Messenger Signaling
气体信使信号的结构生物学
  • 批准号:
    8142890
  • 财政年份:
    2008
  • 资助金额:
    $ 28.83万
  • 项目类别:
Structural Biology of Gaseous Messenger Signaling
气体信使信号的结构生物学
  • 批准号:
    7528507
  • 财政年份:
    2008
  • 资助金额:
    $ 28.83万
  • 项目类别:
STRUCTURAL BASIS OF CELLULAR SIGNALING
细胞信号传导的结构基础
  • 批准号:
    7721965
  • 财政年份:
    2008
  • 资助金额:
    $ 28.83万
  • 项目类别:
STRUCTURAL BASIS FOR SIGNAL TRANSDUCTION BY HEMOPROTEIN SENSORS
血蛋白传感器信号转导的结构基础
  • 批准号:
    7597892
  • 财政年份:
    2007
  • 资助金额:
    $ 28.83万
  • 项目类别:
STRUCTURAL BASIS OF CELLULAR SIGNALING
细胞信号传导的结构基础
  • 批准号:
    7598220
  • 财政年份:
    2007
  • 资助金额:
    $ 28.83万
  • 项目类别:
STRUCTURAL BASIS FOR SIGNAL TRANSDUCTION BY HEMOPROTEIN SENSORS
血蛋白传感器信号转导的结构基础
  • 批准号:
    7370336
  • 财政年份:
    2006
  • 资助金额:
    $ 28.83万
  • 项目类别:

相似国自然基金

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
  • 批准年份:
    2019
  • 资助金额:
    55.0 万元
  • 项目类别:
    面上项目

相似海外基金

Targeting protein arginine methylation in the 9p21.3 loss tumor microenvironment
9p21.3 缺失肿瘤微环境中的靶向蛋白精氨酸甲基化
  • 批准号:
    489995
  • 财政年份:
    2023
  • 资助金额:
    $ 28.83万
  • 项目类别:
    Operating Grants
The role of protein arginine methyl transferase PRMT1 on myelin development
蛋白精氨酸甲基转移酶PRMT1对髓磷脂发育的作用
  • 批准号:
    23K14287
  • 财政年份:
    2023
  • 资助金额:
    $ 28.83万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
Normalizing arginine metabolism with sepiaptein for immunostimulatory-shift ofHER2+ breast cancer
使用 Sepiaptein 使精氨酸代谢正常化以实现 HER2 乳腺癌的免疫刺激转变
  • 批准号:
    10776256
  • 财政年份:
    2023
  • 资助金额:
    $ 28.83万
  • 项目类别:
Effects of Arginine Depletion Combined with Platinum-Taxane Chemotherapy in Aggressive Variant Prostate Cancers (AVPC)
精氨酸消耗联合铂类紫杉烷化疗对侵袭性变异前列腺癌 (AVPC) 的影响
  • 批准号:
    10715329
  • 财政年份:
    2023
  • 资助金额:
    $ 28.83万
  • 项目类别:
Understanding resistance mechanisms to protein arginine methyltransransferase Inhibitors in Lymphoma
了解淋巴瘤对蛋白精氨酸甲基转移酶抑制剂的耐药机制
  • 批准号:
    10668754
  • 财政年份:
    2023
  • 资助金额:
    $ 28.83万
  • 项目类别:
Targeting protein arginine methylation in the 9p21.3 loss tumor microenvironment
9p21.3 缺失肿瘤微环境中的靶向蛋白精氨酸甲基化
  • 批准号:
    498862
  • 财政年份:
    2023
  • 资助金额:
    $ 28.83万
  • 项目类别:
    Operating Grants
Physiological function of arginine signaling:macropinocytosisand tumor immune evasion
精氨酸信号的生理功能:巨胞饮作用与肿瘤免疫逃避
  • 批准号:
    23H03317
  • 财政年份:
    2023
  • 资助金额:
    $ 28.83万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Regulation of androgen receptor signaling in prostate cancer by protein arginine methylation
通过蛋白质精氨酸甲基化调节前列腺癌中的雄激素受体信号传导
  • 批准号:
    10584689
  • 财政年份:
    2023
  • 资助金额:
    $ 28.83万
  • 项目类别:
Arginine methylation of the RNA helicase DDX5 in the regulation of RNA/DNA hybrids during the DNA damage response.
RNA 解旋酶 DDX5 的精氨酸甲基化在 DNA 损伤反应期间调节 RNA/DNA 杂交体中的作用。
  • 批准号:
    487619
  • 财政年份:
    2023
  • 资助金额:
    $ 28.83万
  • 项目类别:
    Operating Grants
Regulation of and Target Recognition by Protein Arginine Methyltransferase 1 (PRMT1)
蛋白质精氨酸甲基转移酶 1 (PRMT1) 的调节和目标识别
  • 批准号:
    10653465
  • 财政年份:
    2023
  • 资助金额:
    $ 28.83万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了