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Membrane Interaction of Mycobacterium tuberculosis Virulence Factors

Membrane Interaction of Mycobacterium tuberculosis Virulence Factors
结核分枝杆菌毒力因子的膜相互作用
批准号:
9902488
负责人:
Jianjun Sun
金额:
$33.98万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-04-08 至 2022-04-30

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中文摘要
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Title: Membrane interaction of Mycobacterium tuberculosis virulence factors PROJECT SUMMARY It is estimated that Mycobacterium tuberculosis (Mtb), a contagious and airborne bacterial pathogen, infects one-third of the world population and causes 1-2 million deaths each year. It is believed that initial Mtb infection occurs in alveolar macrophages. Mtb is internalized into the phagosome, where it penetrates the phagosomal membrane and translocates into the cytosol for replicating and cell-to-cell spreading. The cytosolic translocation is regarded as an important mechanism of Mtb pathogenesis. Two Mtb virulence factors, namely 6-kDal early antigenic target (MtbESAT6) and 10-kDal culture filtrate protein (MtbCFP10), are secreted out of Mtb as a heterodimer and have been implicated to play an essential role in Mtb cytosolic translocation. Genetic knockout of either esat-6 or cfp-10 results in defective cytosolic translocation and attenuated virulence. Our recent studies have suggested that MtbESAT-6 has an acidic-pH dependent pore- forming activity that is required for Mtb cytosolic translocation and virulence. However, the molecular mechanisms governing MtbESAT-6 pore formation and heterodimer dissociation are not clear. In the present proposal, using a variety of biochemical, microscopic, structural and cellular approaches, we will probe the dynamic process of MtbESAT-6 pore formation and determine the structure of the pore complex. We will also investigate the role of Nα-acetylation of MtbESAT-6 in acidification-induced heterodimer dissociation, a prerequisite for MtbESAT-6 to interact with the membrane. Studies designed in this grant proposal are aimed to fill the critical gap in our understanding of the MtbESAT-6-dependent molecular events during Mtb infection in alveolar macrophages and other phagocytes. Knowledge obtained from the proposed studies will facilitate the development of novel countermeasures, therapeutics and vaccines, against tuberculosis. !
期刊论文(3)
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会议论文
DOI: 10.3390/toxins8020034
发表时间: 2016-01-22
期刊: Toxins
影响因子: 4.2
作者: [Sun J, Jacquez P]
通讯作者: Jacquez P
DOI: 10.3390/cells10071645
发表时间: 2021-06-30
期刊: Cells
影响因子: 6
作者: [Bao Y, Wang L, Sun J]
通讯作者: Sun J
Physiological Functions of Female Reproductive Tract Secretions
  • 批准号:
    10377436
  • 项目类别:
  • 资助金额:
    $32.74万
  • 财政年份:
    2020
  • 负责人:
    Jianjun Sun
  • 依托单位:
Physiological Functions of Female Reproductive Tract Secretions
Genetic interrogation of conserved follicular factors for matrix metalloproteinase regulation and ovulation
Genetic interrogation of conserved follicular factors for matrix metalloproteinase regulation and ovulation
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