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Extracellular serine protease cascades modulate protective responses to limit bleeding and infection in vertebrate and invertebrate animals, but our understanding of these pathways in insects is rudimentary at best. Previous work from this laboratory has established the lepidopteran insect, Manduca sexta, as a model system well suited for biochemical characterization of the complex functions of hemolymph proteases. Experiments in this proposal are designed to investigate the roles of plasma serine proteases and their inhibitors (serpins) in insect innate immune responses, including activation of phenoloxidase. The work will test hypotheses based on the following model. Pattern recognition proteins in plasma bind to microbial surfaces. These proteins then interact with serine protease zymogens and other protein cofactors to form protein complexes, which localize the protease cascade and subsequent melanin deposition to the foreign surface. Separate pathways (or separate branches of converging pathways) may be initiated by different types of microorganisms, as they are recognized by separate sets of pattern recognition proteins. Inhibition of the proteases by specific interactions with serpins limit the duration and location of the response. The specific aims of the projectare: 1. Investigate the activation of selected clip domain proteases and their inhibition by specific serpins, to determine their order in microbe-activated cascade pathways. 2. Identify protein interactions that result in formation of protease activation complexes and investigate the assembly of such complexes and their roles in localizing phenoloxidase activation on surfaces. Relevance: Innate immune responses are likely to affect the outcome of infections of insect vectors with the pathogens and parasites they transmit. The long term goals of the research are to gain a thorough understanding of the protease cascades that mediate innate immune responses in M. sexta, to apply this knowledge to insect vectors of human diseases, and to apply advantages of the M. sexta system for fundamental studies on the regulation of serine protease activity.
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会议论文
DOI: 10.1016/j.ibmb.2010.07.002
发表时间: 2010-10
期刊: INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY
影响因子: 3.8
作者: [Zhu, Yifei, Ragan, Emily J., Kanost, Michael R.]
通讯作者: Kanost, Michael R.
DOI: 10.1016/j.cois.2015.09.003
发表时间: 2015-10-01
期刊: Current opinion in insect science
影响因子: 5.3
作者: [Kanost MR, Jiang H]
通讯作者: Jiang H
DOI: 10.1016/j.ibmb.2015.01.015
发表时间: 2015-07
期刊: INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY
影响因子: 3.8
作者: [He, Yan, Cao, Xiaolong, Li, Kai, Hu, Yingxia, Chen, Yun-ru, Blissard, Gary, Kanost, Michael R., Jiang, Haobo]
通讯作者: Jiang, Haobo
Exchangeable apolipoproteins of insects share a common structural motif.
昆虫的可交换载脂蛋白具有共同的结构基序。
DOI: --
发表时间: 1994
期刊: Journal of lipid research
影响因子: 6.5
作者: [Smith,AF, Owen,LM, Strobel,LM, Chen,H, Kanost,MR, Hanneman,E, Wells,MA]
通讯作者: Wells,MA
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    Function of hemolymph plasma proteins in insect immune responses
    • 批准号:
      10207099
    • 项目类别:
    • 资助金额:
      $42.49万
    • 财政年份:
      2021
    • 负责人:
      Michael R Kanost
    • 依托单位:
    Function of hemolymph plasma proteins in insect immune responses
    • 批准号:
      10569087
    • 项目类别:
    • 资助金额:
      $37.67万
    • 财政年份:
      2021
    • 负责人:
      Michael R Kanost
    • 依托单位:
    Function of hemolymph plasma proteins in insect immune responses
    • 批准号:
      10578375
    • 项目类别:
    • 资助金额:
      $2.04万
    • 财政年份:
      2021
    • 负责人:
      Michael R Kanost
    • 依托单位:
    Function of hemolymph plasma proteins in insect immune responses (Equipment Supplement)
    • 批准号:
      10793686
    • 项目类别:
    • 资助金额:
      $3.6万
    • 财政年份:
      2021
    • 负责人:
      Michael R Kanost
    • 依托单位:
    海外基金