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克氏锥虫:针对细胞骨架的单克隆抗体可识别鞭毛附着区的巨大蛋白质。

Trypanosoma cruzi: monoclonal antibody to cytoskeleton recognizes giant proteins of the flagellar attachment zone.

作者信息

Ruiz-Moreno L, Bijovsky A T, Pudles J, Alves M J, Colli W

机构信息

Universidad Nacional de Córdoba, Argentina.

出版信息

Exp Parasitol. 1995 Jun;80(4):605-15. doi: 10.1006/expr.1995.1076.

Abstract

Cytoskeletal preparations of Trypanosoma cruzi trypomastigotes and epimastigotes contain a protein recognized by a monoclonal antibody (2G4) which is connected to the flagellar attachment zone of both stages of the parasite. Western blot analysis revealed that the antibody was able to recognize protein bands of molecular masses higher than 700 kDa up to 2500 kDa. These giant proteins do not seem to share sequences with beta-connectin since an anti-beta-connectin antibody did not recognize the T. cruzi proteins nor did the 2G4 monoclonal antibody recognize authentic beta-connectin. Immunofluorescence and immunogold electron microscopy provided evidence that this protein is located inside the cell body of the parasite, closely related to a corset of four microtubules known as subpellicular microtubule quartet. Immunogold labeling shows that the protein accompanies the flagellar attachment zone as long as the flagellum adheres to the cell body. It is proposed that these microtubule-associated proteins recognized by the 2G4 monoclonal antibody exist only in trypanosomatid forms having a junctional complex between the flagellum and the cell body and may act as transmembrane elements connecting the subpellicular microtubular quartet with the flagellum at the desmosome region.

摘要

克氏锥虫锥鞭毛体和上鞭毛体的细胞骨架制剂含有一种可被单克隆抗体(2G4)识别的蛋白质,该蛋白质与寄生虫这两个阶段的鞭毛附着区相连。蛋白质印迹分析表明,该抗体能够识别分子量高于700 kDa直至2500 kDa的蛋白条带。这些巨大的蛋白质似乎不与β-连接蛋白共享序列,因为抗β-连接蛋白抗体不能识别克氏锥虫蛋白,2G4单克隆抗体也不能识别真正的β-连接蛋白。免疫荧光和免疫金电子显微镜提供了证据,表明这种蛋白质位于寄生虫的细胞体内,与称为表膜下微管四重体的四条微管束紧密相关。免疫金标记显示,只要鞭毛附着在细胞体上,该蛋白质就伴随着鞭毛附着区。有人提出,被2G4单克隆抗体识别的这些微管相关蛋白仅存在于鞭毛与细胞体之间具有连接复合体的锥虫类形态中,并且可能作为跨膜元件在桥粒区域将表膜下微管四重体与鞭毛连接起来。

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