Steffen W, Linck R W
Department of Cell Biology and Neuroanatomy, University of Minnesota, Minneapolis 55455.
Cell Motil Cytoskeleton. 1989;14(3):359-71. doi: 10.1002/cm.970140306.
Affinity-purified antibodies raised against three flagellar tektins (tektin A, B, and C) from each of two sea urchin species (Lytechinus pictus and Strongylocentrotus purpuratus) were used to study the immunological relationship between tektins and intermediate filament proteins. By immunofluorescence microscopy, several antitektins revealed a staining of intermediate filament-like arrays in three vertebrate cell lines tested. Immunoelectron microscopy substantiated the cross reaction of antitektins with intermediate filaments. When the cells were treated with cytochalasin B, the arrangement of the filaments recognized by anti-(Lp)-tektin B was altered; the alteration observed is typical for keratin filaments. By immunoblot, it was found that anti-(Lp)-tektin B cross reacted with two isoforms or different proteins of approximately 54 kD with pIs of 6.1 and 6.2 in human carcinoma epithelia (HeLa) cells and with two isoforms or different proteins of approximately 55 kD with pIs of 6.1 and 6.3 in pig kidney epithelia (LLC-PK1) cells. Furthermore, when antitektin antibodies were affinity purified with the 54 kD HeLa keratin, these keratin-specific antibodies again restained the original tektins on immunoblots. From these observations, it can be concluded that tektins and keratins are to a certain extent immunologically related. To determine the degree of the immunological relationship, tektin filaments and purified intermediate filaments from HeLa cells were cleaved with alpha-chymotrypsin and examined by quantitative immunoblot analysis. On immunoblots of digested tektins from L. pictus, anti-(Lp)-tektin B recognized several cleavage products in the range of 20 kD to 46 kD. However, when immunoblots of digested intermediate filaments from HeLa cells were probed, the cross reaction of anti-(Lp)-tektin B with HeLa keratins was eliminated by more than 98% within 2 min, suggesting that tektins have epitopes in common with the end domains of certain keratins.
针对两种海胆(刺冠海胆和紫球海胆)的三种鞭毛轴纤丝蛋白(轴纤丝蛋白A、B和C)制备的亲和纯化抗体,用于研究轴纤丝蛋白与中间丝蛋白之间的免疫关系。通过免疫荧光显微镜观察,几种抗轴纤丝蛋白抗体在三种受试脊椎动物细胞系中显示出中间丝样阵列的染色。免疫电子显微镜证实了抗轴纤丝蛋白与中间丝的交叉反应。当用细胞松弛素B处理细胞时,抗(刺冠海胆)轴纤丝蛋白B识别的丝的排列发生了改变;观察到的这种改变是角蛋白丝的典型特征。通过免疫印迹发现,抗(刺冠海胆)轴纤丝蛋白B与人癌上皮细胞(HeLa)中两种约54 kD、等电点分别为6.1和6.2的同工型或不同蛋白质发生交叉反应,与猪肾上皮细胞(LLC-PK1)中两种约55 kD、等电点分别为6.1和6.3的同工型或不同蛋白质发生交叉反应。此外,当用54 kD的HeLa角蛋白对抗轴纤丝蛋白抗体进行亲和纯化时,这些角蛋白特异性抗体在免疫印迹上再次对原来的轴纤丝蛋白进行了染色。从这些观察结果可以得出结论,轴纤丝蛋白和角蛋白在一定程度上存在免疫相关性。为了确定免疫相关程度,用α-胰凝乳蛋白酶切割刺冠海胆的轴纤丝蛋白丝和HeLa细胞纯化的中间丝,并通过定量免疫印迹分析进行检测。在刺冠海胆消化后的轴纤丝蛋白免疫印迹上,抗(刺冠海胆)轴纤丝蛋白B识别出20 kD至46 kD范围内的几种切割产物。然而,当用HeLa细胞消化后的中间丝免疫印迹进行检测时,抗(刺冠海胆)轴纤丝蛋白B与HeLa角蛋白的交叉反应在2分钟内消除了98%以上,这表明轴纤丝蛋白与某些角蛋白的末端结构域具有共同的表位。