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中文摘要
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描述(由申请方提供):人类病原体对抗感染药物的耐药性对人类健康构成严重威胁,需要持续努力开发新疗法。类异戊二烯生物合成所必需的甲基异戊烯磷酸(MEP)途径广泛存在于人类病原体中,包括由M.结核病和恶性疟原虫。这一途径中的几种酶催化了前所未有的反应,使它们成为开发选择性抑制剂的靶点。我们的长期目标是了解MEP途径中的催化作用,以开发针对病原体中类异戊二烯生物合成的抑制剂。该提案描述了研究三个有趣的MEP途径酶,IspG,DXP合酶和IspF。具体目标1和3侧重于产生和利用环二磷酸中间体甲基环二磷酸(MEcPP)的酶的机制研究和抑制剂开发。具体目标2的目标是了解DXP合酶在C-N键形成中的催化作用,以产生药用的异羟肟酸化合物类。针对这些酶开发的抗感染药物有可能广泛影响致命传染病的治疗。 公共卫生相关性:人类病原体的耐药性是一个全球性的健康问题,需要持续努力开发治疗威胁生命的感染的新策略。 拟议的研究检查了在人类病原体中广泛存在的机制上有趣的必需甲基磷酸途径酶。这些酶的机制研究将导致新的抗感染药物的开发。
英文摘要
DESCRIPTION (provided by applicant): Resistance of human pathogens to anti-infective agents poses a serious threat to human health and requires sustained efforts to develop new therapies. The essential methylerythritol phosphate (MEP) pathway for isoprenoid biosynthesis is widespread in human pathogens, including some of the most deadly infections caused by M. tuberculosis and P. falciparum. Several of the enzymes in this pathway catalyze unprecedented reactions, making them particularly attractive as targets for the development of selective inhibitors. Our long term goal is to understand catalysis in the MEP pathway toward the development of inhibitors targeting isoprenoid biosynthesis in pathogens. This proposal describes studies to examine three intriguing MEP pathway enzymes, IspG, DXP synthase and IspF. Specific Aims 1 and 3 focus on mechanistic studies and inhibitor development of the enzymes that generate and utilize cyclodiphosphate intermediate, methylerythritol cyclodiphosphate (MEcPP). The goal of Specific Aim 2 is to understand catalysis of DXP synthase in C-N bond formation to generate the medicinally useful hydroxamic acid compound class. Anti-infective agents developed to target these enzymes have the potential to broadly impact the treatment of deadly infectious diseases. PUBLIC HEALTH RELEVANCE: Drug resistance in human pathogens is a global health concern requiring sustained efforts to develop new strategies for treatment of life threatening infections. The proposed studies examine the mechanistically intriguing essential methylerythritol phosphate pathway enzymes which are widespread in human pathogens. Mechanistic studies of these enzymes will lead to the development of new anti-infective agents.
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Toward understanding the chemistry and biology of microbial DXP synthase
  • 批准号:
    10641824
  • 项目类别:
  • 资助金额:
    $40.33万
  • 财政年份:
    2021
  • 负责人:
    Caren L. Freel Meyers
  • 依托单位:
Targeting DXP synthase in bacterial metabolism
  • 批准号:
    10576858
  • 项目类别:
  • 资助金额:
    $57.62万
  • 财政年份:
    2021
  • 负责人:
    Caren L. Freel Meyers
  • 依托单位:
Targeting DXP synthase in bacterial metabolism
  • 批准号:
    10372207
  • 项目类别:
  • 资助金额:
    $57.62万
  • 财政年份:
    2021
  • 负责人:
    Caren L. Freel Meyers
  • 依托单位:
Toward understanding the chemistry and biology of microbial DXP synthase
  • 批准号:
    10470350
  • 项目类别:
  • 资助金额:
    $39.89万
  • 财政年份:
    2021
  • 负责人:
    Caren L. Freel Meyers
  • 依托单位:
海外基金