Fujii T, Takagi H, Arimoto M, Ootani H, Ueeda T
Department of Kansei Engineering, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano 386-8567, Japan.
J Biochem. 2000 Mar;127(3):457-65. doi: 10.1093/oxfordjournals.jbchem.a022628.
Smooth muscle basic calponin, a major actin-, tropomyosin-, and calmodulin-binding protein, has been examined for its ability to interact with desmin intermediate filaments from smooth muscle cells using sedimentation analysis, turbidity changes, chemical cross-linking, matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI TOF/MS), and electron microscopic observations. Calponin interacted with desmin intermediate filaments in a concentration-dependent manner in vitro. The binding of calponin to desmin produced dense aggregates at 30 degrees C. The dense aggregates were observed by electron microscopy to be composed of large anisotropic bundles of desmin filaments, indicating that calponin forms bundles of desmin filaments. The addition of calmodulin or S100 to the mixture of calponin and desmin caused the removal of calponin from the desmin filaments and inhibited bundle formation in the presence of Ca(2+), but not in the presence of EGTA. Calponin-related proteins including G-actin, tropomyosin, and SM22, had little effect on the binding of calponin to desmin filaments, whereas tubulin weakly inhibited the binding. Desmin had little influence on the calponin-actin and calponin-tubulin interactions using the zero-length cross-linker, EDC. Domain mapping with chymotryptic digestion showed that the binding site of calponin resides within the central a-helical rod domain of the desmin molecule. The chemical cross-linked products of calponin and synthetic peptides (TQ27, TNEKVELQELNDRFANYIEKVRFLEQQ; EE24, EEELRELRRQVDALTGQRARVEVE) derived from the rod domain were detected by MALDI TOF/MS. Furthermore, the calponin-desmin interaction was significantly inhibited by the addition of EE24, but only slightly by TQ27. These results suggest that calponin may act as a cross-linking protein between desmin filaments as well as among intermediate filaments, microfilaments and microtubules in smooth muscle cells.
平滑肌碱性调宁蛋白是一种主要的肌动蛋白、原肌球蛋白和钙调蛋白结合蛋白,已通过沉降分析、浊度变化、化学交联、基质辅助激光解吸电离飞行时间质谱(MALDI TOF/MS)和电子显微镜观察,研究了其与平滑肌细胞结蛋白中间丝相互作用的能力。在体外,调宁蛋白以浓度依赖的方式与结蛋白中间丝相互作用。调宁蛋白与结蛋白的结合在30℃时产生致密聚集体。通过电子显微镜观察到致密聚集体由结蛋白丝的大的各向异性束组成,表明调宁蛋白形成结蛋白丝束。在钙调蛋白和结蛋白的混合物中加入钙调蛋白或S100会导致调宁蛋白从结蛋白丝上解离,并在有Ca(2+)存在时抑制束形成,但在有乙二醇双乙醚二胺四乙酸(EGTA)存在时则不会。包括G-肌动蛋白、原肌球蛋白和SM22在内的与调宁蛋白相关的蛋白质对调宁蛋白与结蛋白丝的结合影响很小,而微管蛋白则微弱地抑制这种结合。使用零长度交联剂1-乙基-3-(3-二甲基氨基丙基)碳二亚胺(EDC)时,结蛋白对调宁蛋白-肌动蛋白和调宁蛋白-微管蛋白的相互作用影响很小。用胰凝乳蛋白酶消化进行结构域定位表明,调宁蛋白的结合位点位于结蛋白分子的中央α-螺旋杆状结构域内。通过MALDI TOF/MS检测到了调宁蛋白与源自杆状结构域的合成肽(TQ27,TNEKVELQELNDRFANYIEKVRFLEQQ;EE24,EEELRELRRQVDALTGQRARVEVE)的化学交联产物。此外,加入EE24可显著抑制调宁蛋白-结蛋白的相互作用,但加入TQ27时仅有轻微抑制作用。这些结果表明,调宁蛋白可能作为一种交联蛋白,存在于平滑肌细胞的结蛋白丝之间以及中间丝、微丝和微管之间。