Molecular expression of biologically active substances produced from newborn larvae of Trichinella
Molecular expression of biologically active substances produced from newborn larvae of Trichinella
批准号:
12670229
负责人:
TAKAHASHI Yuzo
金额:
$1.09万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
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
中文摘要
旋毛虫具有许多生物活性物质,其中一些可能具有独特的特性,并可能用于实验和制药目的。我们已经克隆并表达了旋毛虫肌幼虫丝氨酸蛋白酶抑制剂。利用基因工程技术大规模生产丝氨酸蛋白酶抑制剂,可能为药物应用和疫苗接种提供新的手段。新生幼虫穿透宿主组织,在宿主体内迁移。通过对肌幼虫和新生幼虫的c DNA文库进行免疫筛选,我们克隆到一个新的排泄-分泌(E-S)蛋白,即肌球蛋白、原肌球蛋白和丝氨酸蛋白酶。重组蛋白在大肠杆菌表达系统中得到表达。丝氨酸蛋白酶和烯醇化酶重组蛋白具有较强的酶活性。重组丝氨酸蛋白酶的酶活性可能主要是纤溶酶样酶活性,我们开发了一种肌源性调节因子MyoD和Mygenin的检测系统。从旋毛虫成囊早期就开始表达MyoD和Mygenin,我们研究了旋毛虫不同发育阶段的基因表达。分析基因包括E-S蛋白和巨噬细胞移动抑制因子。这些蛋白在不同发育阶段的表达水平存在较大差异,今后我们将从旋毛虫的cDNA文库中寻找更多有用的蛋白,并利用在昆虫细胞中表达的重组蛋白来研究这些蛋白的功能。
英文摘要
Trichinella have a number of biologically active substances, some of which may be endowed with unique characteristics and possible usage for experimental and pharmaceutical purposes. We have already cloned and expressed a serine proteinase inhibitor of T. spiralis of muscle larvae. Mass production of serine proteinase inhibitor by genetic engineering may provide a new means for pharmaceutical usage and vaccine.Newborn larvae penetrate the host tissue and migrate through the body of the host. As a result of immunoscreening of the cDNA library constructed from not only muscle larvae but also newborn larvae, we could clone a novel excretory-secretory (E-S) protein, myosin, tropomyosin and serine proteinase. The recombinant proteins were produced in an Escherichia coli expression system. The recombinant protein of serine proteinase and enolase exhibited enzymatic activity. The enzymatic activity of recombinant serine proteinase could be mainly plasmin-like proteinase activity.We developed a detection system for myogenic regulatory factors such as MyoD and myogenin. MyoD and myogenin were expressed from the early phase of cystogenesis in Trichinella infection.We investigated gene expression at different developmental stages of Trichinella. The analysis genes included E-S proteins and macrophage migration inhibitory factor. There were many differences in the expression level of these proteins at different developmental stages.After this, we would like to search more useful proteins from Trichinella cDNA library, and study the function of these proteins by using the recombinant proteins expressed in insect cells.
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Zhiliang Wu: "Expression of MyoD and myogenin in muscles of mice experimentally infected with Trichinella spiralis or Trichinella pseudospiralis"Parasite. 8. S51-53 (2001)
吴志良:“实验感染旋毛虫或假旋毛虫的小鼠肌肉中MyoD和肌细胞生成素的表达”寄生虫。
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通讯作者:
Isao Nagano: "Molecular cloning and characterization of a novel protein of Trichinella pseudospiralis excretory-secretory products"Journal of Helminthology. (in press.). (2002)
Isao Nagano:“假旋毛虫排泄物分泌产物的新型蛋白质的分子克隆和表征”蠕虫学杂志。
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作者:
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通讯作者:
Zhiliang Wu: "Expression of MyoD and myogenin in muscles of mice experimentally infected with Trichinella spiralis or Trichinella pseudospiralis"Parasite. 8. S51-S53 (2001)
吴志良:“实验感染旋毛虫或假旋毛虫的小鼠肌肉中MyoD和肌细胞生成素的表达”寄生虫。
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通讯作者:
Isao Nagano: "Molecular cloning and characterization of a novel protein of Triohinella psevdospirazis excretory-secretory products"Journal of Helmintholosy. 76(in press). (2002)
Isao Nagano:“拟螺旋丝虫排泄物的新型蛋白质的分子克隆和表征”蠕虫杂志。
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作者:
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通讯作者:
Isao Nagano: "Molecular cloning and characterization of a novel protein of Trichinella pseudospiralis excretory-secretory products"Journal of Helminthology. 76(in press). (2002)
Isao Nagano:“假旋毛虫排泄物分泌产物的新型蛋白质的分子克隆和表征”蠕虫学杂志。
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