Klinglmayr Eva, Wenger Julia, Mayr Sandra, Bossy-Wetzel Ella, Puehringer Sandra
Department of Molecular Biology, University of Salzburg, 5020 Salzburg, Austria.
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2012 Oct 1;68(Pt 10):1217-21. doi: 10.1107/S174430911203607X. Epub 2012 Sep 26.
The mechano-enzyme dynamin-related protein 1 plays an important role in mitochondrial fission and is implicated in cell physiology. Dysregulation of Drp1 is associated with abnormal mitochondrial dynamics and neuronal damage. Drp1 shares structural and functional similarities with dynamin 1 with respect to domain organization, ability to self-assemble into spiral-like oligomers and GTP-cycle-dependent membrane scission. Structural studies of human dynamin-1 have greatly improved the understanding of this prototypical member of the dynamin superfamily. However, high-resolution structural information for full-length human Drp1 covering the GTPase domain, the middle domain and the GTPase effector domain (GED) is still lacking. In order to obtain mechanistic insights into the catalytic activity, a nucleotide-free GTPase-GED fusion protein of human Drp1 was expressed, purified and crystallized. Initial X-ray diffraction experiments yielded data to 2.67 Å resolution. The hexagonal-shaped crystals belonged to space group P2(1)2(1)2, with unit-cell parameters a = 53.59, b = 151.65, c = 43.53 Å, one molecule per asymmetric unit and a solvent content of 42%. Expression of selenomethionine-labelled protein is currently in progress. Here, the expression, purification, crystallization and X-ray diffraction analysis of the Drp1 GTPase-GED fusion protein are presented, which form a basis for more detailed structural and biophysical analysis.
机械酶动力相关蛋白1在线粒体分裂中起重要作用,并与细胞生理学相关。Drp1的失调与线粒体动力学异常和神经元损伤有关。就结构域组织、自组装成螺旋状寡聚体的能力以及GTP循环依赖性膜分裂而言,Drp1与动力蛋白1在结构和功能上具有相似性。人类动力蛋白1的结构研究极大地增进了对动力蛋白超家族这一典型成员的理解。然而,仍然缺乏涵盖GTPase结构域、中间结构域和GTPase效应结构域(GED)的全长人类Drp1的高分辨率结构信息。为了深入了解催化活性的机制,表达、纯化并结晶了人类Drp1的无核苷酸GTPase-GED融合蛋白。初步的X射线衍射实验得到了分辨率为2.67 Å的数据。六边形晶体属于空间群P2(1)2(1)2,晶胞参数a = 53.59,b = 151.65,c = 43.53 Å,每个不对称单元有一个分子,溶剂含量为42%。目前正在进行硒代甲硫氨酸标记蛋白的表达。在此,展示了Drp1 GTPase-GED融合蛋白的表达、纯化、结晶和X射线衍射分析,这为更详细的结构和生物物理分析奠定了基础。