Birkenberger L, Ip W
Department of Anatomy and Cell Biology, University of Cincinnati College of Medicine, Ohio 45267-0521.
J Cell Biol. 1990 Nov;111(5 Pt 1):2063-75. doi: 10.1083/jcb.111.5.2063.
Intermediate filament (IF) proteins have a common structural motif consisting of an alpha-helical rod domain flanked by non-alpha-helical amino-terminal head and carboxy-terminal tail domains. Coiled-coil interaction between neighboring rod domains is though to generate the backbone of the 10-nm filament. There must also be other interactions between subunits to bring them into alignment and to effect elongation of the filament, but these are poorly understood. To examine the involvement of the tail domain in filament structure and stabilization, we have studied the interaction between a synthetic peptide corresponding to residues 442-450 of avian desmin, and authentic desmin protein. The potential importance of this region lies in its hydrophilic nature and its high degree of homology among the Type III IF proteins and cytokeratins 8 and 18. The peptide, D442-450, binds to a 27-residue region between lys-436 and leu-463, the carboxy terminus. The presence of the peptide during assembly causes the filaments to appear much more loosely packed than normal desmin IF. We have also generated polyclonal antibodies against this peptide and attempted to localize this portion of the tailpiece along desmin IFs by immunological procedures. By immunoblotting, we found that anti-D442-450 antibodies recognize desmin and only those proteolytic fragments that contain the tailpiece. In contrast, the antibodies do not label any structure in adult gizzard smooth muscle and skeletal muscle myofibrils in immunofluorescence experiments during which conventional antidesmin antibodies do. At the ultrastructural level, anti-D442-450 antibodies label free desmin tetramers but not desmin IFs. These results show that, as part of an assembled IF, the epitope of anti-D442-450 is inaccessible to the antibodies, and suggest that either the tailpiece of an IF protein may not be entirely peripheral to the filament backbone, or the interaction between end domains during assembly masks this particular region of the IF molecule.
中间丝(IF)蛋白具有共同的结构基序,由一个α螺旋杆状结构域以及位于其两侧的非α螺旋氨基末端头部和羧基末端尾部结构域组成。相邻杆状结构域之间的卷曲螺旋相互作用被认为产生了10纳米细丝的主干。亚基之间还必定存在其他相互作用,以使它们排列整齐并实现细丝的延长,但这些相互作用目前还了解甚少。为了研究尾部结构域在细丝结构和稳定性中的作用,我们研究了与禽结蛋白442 - 450位残基相对应的合成肽与天然结蛋白之间的相互作用。该区域的潜在重要性在于其亲水性以及在III型中间丝蛋白与细胞角蛋白8和18之间的高度同源性。肽D442 - 450与羧基末端lys - 436和leu - 463之间的27个残基区域结合。在组装过程中该肽的存在使细丝看起来比正常的结蛋白中间丝堆积得更为松散。我们还针对该肽产生了多克隆抗体,并试图通过免疫学方法将尾段的这一部分定位在结蛋白中间丝上。通过免疫印迹,我们发现抗D442 - 450抗体识别结蛋白以及仅那些包含尾段的蛋白水解片段。相比之下,在免疫荧光实验中,当传统的抗结蛋白抗体能够标记成年砂囊平滑肌和骨骼肌肌原纤维中的任何结构时,这些抗体却不能。在超微结构水平上,抗D442 - 450抗体标记游离的结蛋白四聚体,但不标记结蛋白中间丝。这些结果表明,作为组装好的中间丝的一部分,抗D442 - 450的表位对抗体不可及,这表明要么中间丝蛋白的尾段可能并非完全位于细丝主干的外周,要么组装过程中末端结构域之间的相互作用掩盖了中间丝分子的这一特定区域。