Department of Biochemistry and Molecular Biology, The Institute for Medical Research Israel-Canada, The Hebrew University-Hadassah Medical School, Jerusalem 91120, Israel.
J Biol Chem. 2010 Mar 5;285(10):7079-86. doi: 10.1074/jbc.M109.049221. Epub 2009 Dec 3.
The motor protein, non-muscle myosin II (NMII), must undergo dynamic oligomerization into filaments to participate in cellular processes such as cell migration and cytokinesis. A small non-helical region at the tail of the long coiled-coil region (tailpiece) is a common feature of all dynamically assembling myosin II proteins. In this study, we investigated the role of the tailpiece in NMII-C self-assembly. We show that the tailpiece is natively unfolded, as seen by circular dichroism and NMR experiments, and is divided into two regions of opposite charge. The positively charged region (Tailpiece(1946-1967)) starts at residue 1946 and is extended by seven amino acids at its N terminus from the traditional coiled-coil ending proline (Tailpiece(1953-1967)). Pull-down and sedimentation assays showed that the positive Tailpiece(1946-1967) binds to assembly incompetent NMII-C fragments inducing filament assembly. The negative region, residues 1968-2000, is responsible for NMII paracrystal morphology as determined by chimeras in which the negative region was swapped between the NMII isoforms. Mixing the positive and negative peptides had no effect on the ability of the positive peptide to bind and induce filament assembly. This study provides molecular insight into the role of the structurally disordered tailpiece of NMII-C in shifting the oligomeric equilibrium of NMII-C toward filament assembly and determining its morphology.
马达蛋白,非肌肉肌球蛋白 II(NMII),必须经历动态寡聚化形成纤维,才能参与细胞迁移和胞质分裂等细胞过程。长卷曲螺旋区尾部的一个小的非螺旋区域(尾部)是所有动态组装的肌球蛋白 II 蛋白的共同特征。在这项研究中,我们研究了尾部在 NMII-C 自组装中的作用。我们表明,尾部是天然无规卷曲的,这可以通过圆二色性和 NMR 实验观察到,并且分为两个带相反电荷的区域。带正电荷的区域(Tailpiece(1946-1967))从残基 1946 开始,其 N 端从传统卷曲螺旋末端脯氨酸延伸了七个氨基酸(Tailpiece(1953-1967))。下拉和沉淀实验表明,阳性 Tailpiece(1946-1967)与组装无能 NMII-C 片段结合诱导纤维组装。阴性区域,残基 1968-2000,负责 NMII 准晶形态,这可以通过在 NMII 同工型之间交换阴性区域的嵌合体来确定。混合阳性和阴性肽对阳性肽结合和诱导纤维组装的能力没有影响。这项研究提供了分子洞察力,了解 NMII-C 结构无序尾部在将 NMII-C 的寡聚平衡向纤维组装转移和确定其形态方面的作用。