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贾第虫肌动蛋白结合蛋白在蓝氏贾第鞭毛虫盘状微丝带边缘的超微结构定位以及α-贾第虫肌动蛋白结合蛋白的核苷酸和推导的蛋白质序列

Ultrastructural localization of giardins to the edges of disk microribbons of Giarida lamblia and the nucleotide and deduced protein sequence of alpha giardin.

作者信息

Peattie D A, Alonso R A, Hein A, Caulfield J P

机构信息

Department of Tropical Public Health, Harvard School of Public Health, Boston, Massachusetts 02115.

出版信息

J Cell Biol. 1989 Nov;109(5):2323-35. doi: 10.1083/jcb.109.5.2323.

Abstract

The giardins are a group of 29-38-kD proteins in the ventral disk of the protozoan parasite Giardia lamblia. The disk attaches the parasite to the host's intestinal epithelium and is composed of parallel, coiled microtubules that are adjacent to the ventral plasma membrane and from which processes called microribbons extend into the cytoplasm; the microribbons are connected by crossbridges. G. lamblia cytoskeletons, consisting of disks and attached flagella, were isolated and used to show that the 29-38-kD proteins separate into five bands by one-dimensional electrophoresis and into 23 species by two-dimensional analysis. Rabbit antibodies raised against a 33-kD protein band, purified by one-dimensional gel electrophoresis and shown to contain three proteins by two-dimensional electrophoresis, recognized 17 proteins by two-dimensional immunoblot analysis. By immunofluorescence these antibodies reacted with the ventral disk but not with the flagella in isolated cytoskeletons. Electron microscopy revealed that the anti-giardin antibodies bound to the edges of the microribbons but not to the microtubules, crossbridges, or other, nondisk structures. Antibodies to tubulin reacted with both the disk and flagella in isolated cytoskeletons but bound only to the microtubules in these structures. The amino-terminal sequence of the 33-kD immunogen was determined and used to construct a DNA oligomer, and the oligomer was used to isolate the alpha giardin gene. The gene was used to hybrid select RNA, and the in vitro translation product from this RNA was precipitated by the antibodies against the 33-kD immunogen. The gene sequence was a single open reading frame of 885 nucleotides that predicted a protein of 33.8 kD. The protein sequence is unique, having no significant homology to two other giardin sequences or to any sequences within the Protein Identification Resource. It is predicted to be 82% alpha helical. The downstream sequence of the gene indicates that the sequence AGT-PuAA is located six to nine nucleotides beyond the stop codon in all protein-encoding genes of G. lamblia that have been sequenced and reported to date.

摘要

贾第虫蛋白是原生动物寄生虫蓝氏贾第鞭毛虫腹盘内一组分子量为29 - 38kD的蛋白质。腹盘将寄生虫附着于宿主肠道上皮,由平行、盘绕的微管组成,这些微管与腹侧质膜相邻,从微管延伸出称为微丝带的突起进入细胞质;微丝带由交叉桥连接。分离出由腹盘和附着的鞭毛组成的蓝氏贾第鞭毛虫细胞骨架,并用于证明29 - 38kD的蛋白质通过一维电泳可分离为五条带,通过二维分析可分离为23种。用一维凝胶电泳纯化并经二维电泳显示含有三种蛋白质的针对一条33kD蛋白带制备的兔抗体,通过二维免疫印迹分析识别出17种蛋白质。通过免疫荧光,这些抗体与分离的细胞骨架中的腹盘反应,但不与鞭毛反应。电子显微镜显示,抗贾第虫蛋白抗体与微丝带边缘结合,但不与微管、交叉桥或其他非腹盘结构结合。抗微管蛋白抗体与分离的细胞骨架中的腹盘和鞭毛都反应,但仅与这些结构中的微管结合。测定了33kD免疫原的氨基末端序列,并用于构建DNA寡聚物,该寡聚物用于分离α贾第虫蛋白基因。该基因用于杂交选择RNA,来自该RNA的体外翻译产物被针对33kD免疫原的抗体沉淀。基因序列是一个885个核苷酸的单一开放阅读框,预测编码一个33.8kD的蛋白质。该蛋白质序列独特,与另外两个贾第虫蛋白序列或蛋白质鉴定资源中的任何序列均无显著同源性。预计其82%为α螺旋结构。该基因的下游序列表明,AGT - PuAA序列位于迄今为止已测序并报道的蓝氏贾第鞭毛虫所有蛋白质编码基因终止密码子下游6至9个核苷酸处。

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