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驱动蛋白在培养细胞中的定位。

Localization of kinesin in cultured cells.

作者信息

Neighbors B W, Williams R C, McIntosh J R

机构信息

Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder 80309.

出版信息

J Cell Biol. 1988 Apr;106(4):1193-204. doi: 10.1083/jcb.106.4.1193.

Abstract

Kinesin was isolated from bovine brain and used to elicit polyclonal antibodies in rabbits. The specificities of the resulting antibodies were evaluated by immunoblotting. Antibodies purified from these sera by their affinity for brain kinesin react with a polypeptide of approximately 120 kD in extracts from bovine brain, PtK1 cells, and mouse neuroblastoma cells. They bind to a pair of polypeptides of approximately 120 kD present in crude kinesin prepared from Xenopus eggs and with a single polypeptide of approximately 115 kD in extracts from Drosophila embryos. Antibodies raised against kinesin prepared from fruit fly embryos (by W. M. Saxton, Indiana University, Bloomington, IN) and from neural tissues of the squid (by M. P. Sheetz, Washington University, St. Louis, MO) cross react with the mammalian, the fly, and the frog polypeptides. Kinesin antigen was localized in cultured cells by indirect immunofluorescence. PtK1 cells in interphase showed dim background staining of cytoplasmic membranous components and bright staining of a small, fibrous, juxtanuclear structure. Double staining with antibodies to microtubules showed that the fibrous object was usually located near the centrosome. On the basis of shape, size, and location, we identify the kinesin-positive structure as a primary cilium. PtK1 cells in mitosis are stained at their poles during all stages of division. The structure stained is approximately spherical, but wisps of faint fluorescence also extend into the body of the spindle. Antibodies to squid or fruit fly kinesin produce identical patterns in PtK1 cells. Controls with preimmune and preabsorbed sera show that the centrosome staining is not due simply to the common tendency of rabbit antisera to stain this structure. Similar centrosome and spindle pole staining was visible when antibodies to bovine brain or squid kinesin were applied to the A6 cell line (kidney epithelial cells from Xenopus laevis). Some possible functions of kinesin localized at the spindle poles are discussed.

摘要

从牛脑中分离出驱动蛋白,并用于在兔体内引发多克隆抗体。通过免疫印迹法评估所得抗体的特异性。从这些血清中通过对脑驱动蛋白的亲和力纯化的抗体,与牛脑、PtK1细胞和小鼠神经母细胞瘤细胞提取物中一条约120kD的多肽发生反应。它们与从非洲爪蟾卵制备的粗制驱动蛋白中存在的一对约120kD的多肽以及果蝇胚胎提取物中一条约115kD的单一多肽结合。针对从果蝇胚胎(由印第安纳大学的W.M.萨克斯顿制备,印第安纳波利斯,印第安纳州)和鱿鱼神经组织(由华盛顿大学的M.P.希茨制备,圣路易斯,密苏里州)制备的驱动蛋白产生的抗体,与哺乳动物、果蝇和青蛙的多肽发生交叉反应。通过间接免疫荧光法将驱动蛋白抗原定位在培养细胞中。处于间期的PtK1细胞显示细胞质膜成分的背景染色较淡,以及一个小的、纤维状的、靠近细胞核的结构染色明亮。用抗微管抗体进行双重染色表明,纤维状物体通常位于中心体附近。根据形状、大小和位置,我们将驱动蛋白阳性结构鉴定为初级纤毛。有丝分裂期的PtK1细胞在分裂的所有阶段其两极都被染色。被染色的结构近似球形,但微弱的荧光束也延伸到纺锤体主体中。针对鱿鱼或果蝇驱动蛋白的抗体在PtK1细胞中产生相同的模式。用免疫前血清和预吸收血清进行的对照表明,中心体染色并非仅仅是兔抗血清染色该结构的常见倾向所致。当将针对牛脑或鱿鱼驱动蛋白的抗体应用于A6细胞系(来自非洲爪蟾的肾上皮细胞)时,可见类似的中心体和纺锤体极染色。讨论了位于纺锤体极的驱动蛋白的一些可能功能。

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