Eilertsen K J, Keller T C
Department of Biological Science, Florida State University, Tallahassee 32306-3050.
J Cell Biol. 1992 Nov;119(3):549-57. doi: 10.1083/jcb.119.3.549.
Two extremely high molecular weight proteins were found to be components of the intestinal epithelial cell brush border cytoskeleton. The largest brush border protein, designated T-protein, migrated on SDS gels as a doublet of polypeptides with molecular weights similar to muscle titin T I and T II. The other large brush border protein, designated N-protein, was found to have a polypeptide molecular weight similar to muscle nebulin. In Western analysis, a polyclonal antibody raised against brush border T-protein reacted specifically with T-protein in isolated brush borders and cross-reacted with titin in pectoralis and cardiac muscle samples. T-protein was distinguished from the muscle titins by an anti-cardiac titin mAb. A polyclonal antibody raised against N-protein was specific for N-protein in brush borders and cross-reacted with nothing in pectoralis muscle. Immunolocalization in cryosections of intestinal epithelia and SDS-PAGE analysis of fractionated brush borders revealed that both T-protein and N-protein are concentrated distinctly in the brush border terminal web region subjacent to the microvilli, but absent from the microvilli. EM of rotary-replicated T-protein samples revealed many of the molecules to be long (912 +/- 40 nm) and fibrous with a globular head on one end. In some of the molecules, the head domain appeared to be extended in a fibrous conformation yielding T-protein up to 1,700-nm long. The brush border N-protein was found as long polymers with a repeating structural unit of approximately 450 nm. Our findings indicate that brush border T-protein is a cellular isoform of titin and suggest that both T-protein and N-protein play structural roles in the brush border terminal web.
发现两种极高分子量的蛋白质是肠上皮细胞刷状缘细胞骨架的组成成分。最大的刷状缘蛋白,命名为T蛋白,在SDS凝胶上迁移时呈现为两条多肽的双峰,其分子量与肌肉肌联蛋白T I和T II相似。另一种大的刷状缘蛋白,命名为N蛋白,其多肽分子量与肌肉伴肌动蛋白相似。在蛋白质免疫印迹分析中,针对刷状缘T蛋白产生的多克隆抗体在分离的刷状缘中与T蛋白特异性反应,并与胸大肌和心肌样本中的肌联蛋白发生交叉反应。通过抗心肌肌联蛋白单克隆抗体将T蛋白与肌肉肌联蛋白区分开来。针对N蛋白产生的多克隆抗体对刷状缘中的N蛋白具有特异性,且与胸大肌中任何物质均无交叉反应。对肠上皮冷冻切片的免疫定位和分级分离的刷状缘的SDS - PAGE分析表明,T蛋白和N蛋白都明显集中在微绒毛下方的刷状缘终末网区域,而微绒毛中不存在。对旋转复制的T蛋白样本进行电子显微镜观察发现,许多分子很长(912±40 nm)且呈纤维状,一端有球状头部。在一些分子中,头部结构域似乎以纤维构象延伸,使T蛋白长达1700 nm。刷状缘N蛋白被发现是长度约为450 nm的重复结构单元的长聚合物。我们的研究结果表明,刷状缘T蛋白是肌联蛋白的细胞异构体,并提示T蛋白和N蛋白在刷状缘终末网中均发挥结构作用。