Norris K A, Schrimpf J E, Szabo M J
Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pennsylvania 15261, USA.
Infect Immun. 1997 Feb;65(2):349-57. doi: 10.1128/iai.65.2.349-357.1997.
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.
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。