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Structure and regulation of the cytoplasmic membrane complexes formed during signal transduction by the Toll-like receptors

Structure and regulation of the cytoplasmic membrane complexes formed during signal transduction by the Toll-like receptors
Toll样受体信号转导过程中形成的细胞质膜复合物的结构和调控
批准号:
BB/G002797/1
负责人:
Nicholas Gay
金额:
$99.31万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2008
资助国家:
英国
项目状态:
已结题
起止时间:
2008 至 --

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中文摘要
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英文摘要
Humans have evolved complex and effective ways of fighting infections caused by microbes such as bacteria and viruses, the immune system. Sometimes the immune system goes wrong and this can cause serious diseases such as rheumatoid arthritis and diabetes. Our research aims to understand at a molecular level how the cells of the immune system are able to recognise microbes and the ways in which these cells respond to cause the familiar symptoms of an infection such as fever and tiredness, and to generate specific antibodies that fight the invading microbes. In this project we will study the way in which immune system cells respond to a powerful toxins, such as endotoxin or LPS, released by certain types of bacteria during an infection. Although normal responses to endotoxin are an important part of the fight against infection, it can cause a highly dangerous condition called endotoxic shock in patients with severe septicaemia and this pathological response frequently causes organ failure and death. In fact endotoxin shock is responsible for about 135000 deaths every year in Europe alone. The proposed studies should shed light on why endotoxin can produce a beneficial reaction in some conditions and a damaging response in others.
期刊论文(10)
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会议论文
DOI: 10.1074/jbc.m110.159996
发表时间: 2011-01-14
期刊: The Journal of biological chemistry
影响因子: --
作者: [George J, Motshwene PG, Wang H, Kubarenko AV, Rautanen A, Mills TC, Hill AV, Gay NJ, Weber AN]
通讯作者: Weber AN
Bioinformatic analysis of Toll-like receptor sequences and structures.
Toll 样受体序列和结构的生物信息分析。
DOI: 10.1007/978-1-59745-541-1_5
发表时间: 2009
期刊: Methods in molecular biology (Clifton, N.J.)
影响因子: --
作者: [Monie TP]
通讯作者: Monie TP
Structure of the glycosyltransferase EryCIII in complex with its activating P450 homologue EryCII.
糖基转移酶红细胞的结构及其激活的P450同源物erycii。
DOI: 10.1016/j.jmb.2011.10.036
发表时间: 2012-01-06
期刊: JOURNAL OF MOLECULAR BIOLOGY
影响因子: 5.6
作者: [Moncrieffe, Martin C., Fernandez, Maria-Jose, Spiteller, Dieter, Matsumura, Hiroyoshi, Gay, Nicholas J., Luisi, Ben F., Leadlay, Peter F.]
通讯作者: Leadlay, Peter F.
MRC-FAPESP: New approaches to the treatment of Paracoccidioidomycosis
  • 批准号:
    MR/S002340/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $72.25万
  • 财政年份:
    2018
  • 负责人:
    Nicholas Gay
  • 依托单位:
Molecular mechanisms of innate immune signal tranduction by the Toll-like receptor 4
  • 批准号:
    G1000133-E01/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $221.95万
  • 财政年份:
    2010
  • 负责人:
    Nicholas Gay
  • 依托单位:
Small molecule agonists and antagonists of inflammatory responses mediated by Toll- and Nod- like receptors
  • 批准号:
    BB/G009295/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $74.95万
  • 财政年份:
    2009
  • 负责人:
    Nicholas Gay
  • 依托单位:
Surface plasmon resonance facility for biochemistry and pharmacology
  • 批准号:
    BB/F01130X/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $30.88万
  • 财政年份:
    2008
  • 负责人:
    Nicholas Gay
  • 依托单位:
国内基金
海外基金
糖尿病ED中成纤维细胞衰老调控内皮细胞线粒体稳态失衡的机制研究
  • 批准号:
    82371634
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    赵福军
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PRNP调控巨噬细胞M2极化并减弱吞噬功能促进子宫内膜异位症进展的机制研究
  • 批准号:
    82371651
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    赵栋
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CBP/p300-HADH轴在基础胰岛素分泌调节中的作用和机制研究
  • 批准号:
    82370798
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    王晓
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精氨酸调控骨髓Tregs稳态在脓毒症骨髓功能障碍中的作用研究
  • 批准号:
    82371770
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    宁铂涛
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