Liu Jun, Taylor Dianne W, Taylor Kenneth A
Institute of Molecular Biophysics, Florida State University, Tallahassee, FL 32306-4380, USA.
J Mol Biol. 2004 Apr 16;338(1):115-25. doi: 10.1016/j.jmb.2004.02.034.
Cryoelectron microscopy was used to obtain a 3-D image at 2.0 nm resolution of 2-D arrays of smooth muscle alpha-actinin. The reconstruction reveals a well-resolved long central domain with 90 degrees of left-handed twist and near 2-fold symmetry. However, the molecular ends which contain the actin binding and calmodulin-like domains, have different structures oriented approximately 90 degrees to each other. Atomic structures for the alpha-actinin domains were built by homology modeling and assembled into an atomic model. Model building suggests that in the 2-D arrays, the two calponin homology domains that comprise the actin-binding domain have a closed conformation at one end and an open conformation at the other end due to domain swapping. The open and closed conformations of the actin-binding domain suggests flexibility that may underlie Ca2+ regulation. The approximately 90 degrees orientation difference at the molecular ends may underlie alpha-actinin's ability to crosslink actin filaments in nearly any orientation.
冷冻电子显微镜用于以2.0纳米的分辨率获得平滑肌α-辅肌动蛋白二维阵列的三维图像。重建结果显示出一个分辨率良好的长中央结构域,具有90度的左旋扭曲和近似2倍对称性。然而,包含肌动蛋白结合结构域和类钙调蛋白结构域的分子末端具有彼此大约成90度的不同结构。通过同源建模构建了α-辅肌动蛋白结构域的原子结构,并组装成一个原子模型。模型构建表明,在二维阵列中,构成肌动蛋白结合结构域的两个钙调蛋白同源结构域由于结构域交换而在一端具有封闭构象,在另一端具有开放构象。肌动蛋白结合结构域的开放和封闭构象表明其具有灵活性,这可能是Ca2+调节的基础。分子末端大约90度的取向差异可能是α-辅肌动蛋白能够以几乎任何取向交联肌动蛋白丝的基础。