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编码160千道尔顿克氏锥虫补体调节蛋白的基因家族的鉴定

Identification of the gene family encoding the 160-kilodalton Trypanosoma cruzi complement regulatory protein.

作者信息

Norris K A, Schrimpf J E, Szabo M J

机构信息

Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pennsylvania 15261, USA.

出版信息

Infect Immun. 1997 Feb;65(2):349-57. doi: 10.1128/iai.65.2.349-357.1997.

Abstract

Trypanosoma cruzi trypomastigotes are exquisitely resistant to the lytic effects of vertebrate complement, and this characteristic contributes to the survival of the parasites in the host bloodstream. Trypomastigotes avoid complement-mediated lysis by the production of a surface glycoprotein that inhibits the formation of the alternative and classical C3 convertase, thus preventing activation and amplification of the complement cascade at the parasite surface. We have developed a monoclonal antibody to the 160-kDa T. cruzi complement regulatory protein (CRP) and describe a one-step immunoaffinity purification procedure. The CRP was purified to homogeneity and subjected to amino-terminal peptide sequence analysis. Based on the protein sequence obtained, the CRP was identified as a member of a large family of trypomastigote-specific genes, and a complete cDNA was isolated and sequenced. The complete coding sequence was cloned in Escherichia coli, and antibodies raised against the full-length recombinant protein reacted specifically with a 160-kDa protein in trypomastigote membrane protein preparations as well as with native, purified CRP. Indirect immunofluorescence revealed that the protein is uniformly expressed at the cell surfaces of trypomastigotes.

摘要

克氏锥虫锥鞭毛体对脊椎动物补体的溶解作用具有极高的抗性,这一特性有助于寄生虫在宿主体内血液中存活。锥鞭毛体通过产生一种表面糖蛋白来避免补体介导的溶解,这种糖蛋白可抑制替代途径和经典途径C3转化酶的形成,从而阻止补体级联反应在寄生虫表面的激活和放大。我们已研制出一种针对160 kDa克氏锥虫补体调节蛋白(CRP)的单克隆抗体,并描述了一种一步免疫亲和纯化方法。CRP被纯化至同质状态,并进行了氨基末端肽序列分析。根据获得的蛋白质序列,CRP被鉴定为锥鞭毛体特异性基因大家族的一员,完整的cDNA被分离并测序。完整的编码序列被克隆到大肠杆菌中,针对全长重组蛋白产生的抗体与锥鞭毛体膜蛋白制剂中的160 kDa蛋白以及天然纯化的CRP发生特异性反应。间接免疫荧光显示该蛋白在锥鞭毛体的细胞表面均匀表达。

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