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Designing of inhibitors for prostaglandin D synthases based on crystallographic analyses

Designing of inhibitors for prostaglandin D synthases based on crystallographic analyses
基于晶体学分析的前列腺素 D 合酶抑制剂的设计
批准号:
12558078
负责人:
URADE Yoshihiro
金额:
$8.77万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2000
资助国家:
日本
项目状态:
已结题
起止时间:
2000 至 2001

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英文摘要
Prostaglandin (PG) D_2 is actively produced in the central nervous system and exhibits a variety of central actions such as sleep induction and pain modulation. POD2 is also produced by mast cells and Th2 cells and is released as an inflammatory and allergic mediator. There are two distinct types of POD synthase (PGDS) : one is lipocalin-type PODS (L-PGDS) localized in the central nervous system and the other is hematopoietic POD synthase (H-PODS) expressed in those allergy-related cells. These two enzymes catalyze the same reaction from POH_2 to POD2 but possess no homology at all in their amno acid sequences. Recombinant mouse L-PGDS and human H-PGDS were cocrystallized with several inhibitors selective to each PODS. We obtained the X-ray diffraction data of these crystals at KEK and Spring-8 synchrotron facilities. The 3-D coordinates of L-PODS complexed with its inhibitor AT-056 were determined at a resolution of 2.5 Å. We also determined the 3-D coordinates of H-PODS complexed wit … More h Mg^<2+> or Ca^<2+> and 4 different inhibitors, including an orally effective inhibitor HQL-79, at 1.2 to 1.8 Å resolution. As predicted, the tertiary structures of two enzymes are quite different from each other L-PGDS possesses β-barrell structure with hydrophobic pocket and H-PGDS, α+β structure with a catalytic creft containing the glutathione-binding site within 2 subdomains. Based on the crystallographic structures, we introduced the site-directed mutagenesis to identify the amino acid residues involved in the catalytic reactions by L-PODS and H-PODS. We then surveyed the functional abnormality of trarisgenic (TG) mice that over-expressed human L-PODS or H-PODS under the control of the β-actin promoter. We found that L-PGDS-TG mice showed a striking time-dependent increase in non-rapid eye movement sleep afler stimulation by tail clipping. The sleep induction in TO mice was positively correlated with the POD2 production in the brain. In an ovalbumin-induced asthma model, L-PODS- or H-PGDS-TG mice showed a pronounced infiltration of eosinophils and lymphocytes into the lung and upregulation of Th2 cytokines in the bronchoalveolar lavage fluid. These TO mice are useful to monitor the in vivo efficacy of the lead compounds to develop the PGDS inhibitors act as anti-doze drugs or anti-allergy drugs. Less
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Fujitani, Y.: "Pronounced eosinophilic lung inflammation and Th2 cytokine release in human liocalin-type prostaglandin D synthase transgenic mice"J Immunol. 0022-1767 (2002)
Fujitani, Y.:“人甘薯苷型前列腺素 D 合酶转基因小鼠中显着的嗜酸性肺部炎症和 Th2 细胞因子释放”J 免疫学杂志。
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通讯作者:
Hirawa, N.: "Urinary prostaglandin D synthase (β-trace) excretion increase in the early-stage of diabetes mellitus"Nephron. 87. 321-327 (2001)
Hirawa, N.:“糖尿病早期尿前列腺素 D 合酶(β-痕量)排泄增加”Nephron 87. 321-327 (2001)
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Inoue, T., et al.: "Serum prostaglandin D synthase level after coronary angioplasty may predict occurrence of restenosis"Thromb Haemost. 85(1). 165-170 (2001)
Inoue, T., et al.:“冠状动脉血管成形术后血清前列腺素 D 合酶水平可以预测再狭窄的发生”Thromb Haemost。
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通讯作者:
Urade, Y. and Hayaishi, O.: "Biochemical, structural, genetic, physiological, and pathophysiological features of lipocalin-type prostaglandin D synthase."Biochim. Biophys. Acta. 1482. 259-271 (2000)
Urade, Y. 和 Hayaishi, O.:“脂运载蛋白型前列腺素 D 合酶的生化、结构、遗传、生理和病理生理学特征。”Biochim。
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41
    Molecular mechanisms of the sleep control by neurons activated during sleep
    Novel function of prostaglandin D2 and its metabolites in pathogenesis of immune and allergic diseases as examined by prostaglandin D synthase gene-manipulated mice
    • 批准号:
      11680642
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.37万
    • 财政年份:
      1999
    • 负责人:
      URADE Yoshihiro
    • 依托单位:
    A new type of the gene-sharing on prostaglandin D synthases
    • 批准号:
      09044352
    • 项目类别:
      Grant-in-Aid for international Scientific Research
    • 资助金额:
      $3.39万
    • 财政年份:
      1997
    • 负责人:
      URADE Yoshihiro
    • 依托单位:
    Functional analysis of secretory prostaglandin D synthase by gene-targeting
    • 批准号:
      07457033
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $4.8万
    • 财政年份:
      1995
    • 负责人:
      URADE Yoshihiro
    • 依托单位:
    海外基金