Taveau J C, Boisset N, Vinogradov S N, Lamy J N
Laboratoire des Protéines Complexes, Université de Tours, 2 bis Boulevard Tonnellé, Tours Cedex, F-37032, France.
J Mol Biol. 1999 Jun 25;289(5):1343-59. doi: 10.1006/jmbi.1999.2824.
A 3D reconstruction of the hemoglobin (Hb) of the earthworm Lumbricus terrestris was carried out by the 3D projection alignment method from electron microscopy images of a frozen-hydrated specimen at 22 A resolution. The results were analyzed by a new approach taking into account the evolution of the 210 densities forming the 3D volume as a function of the threshold of surface representation. The whole oligomer with D6point-group symmetry is comprised of 12 hollow globular substructures (HGS) with local 3-fold symmetry tethered to a complex network of linking subunits (linker complex). The 12 globin subunits of each HGS are distributed around local 3-fold axis in four layers of three subunits. The first layer, the most external, contains monomeric globin chains 2A, 3A, and 5A. The three trimers corresponding to the nine remaining subunits have one subunit in each of the second (2B, 3B, 5B), third (1A, 4A, 6A), and fourth (1B, 4B, 6B) layer. The distances between the centers of the globin chains forming the trimers are in the ranges 20-32 A and 45-52 A. The linker complex is made up of two types of linking units. The first type forms three loops connecting globin chains of the second, third and fourth layers. The average molecular mass (Mm) of these subunits was 25 kDa. The second type forms the central structure, termed hexagonal toroid, and its 12 connections to the HGS. This structure corresponds to a hexamer of a single linking unit with a Mm (31.2 kDa), size and a shape different from those of the HGS loops. A careful study of 3D volume architecture shows that each toroid linking unit is bound to the three loops of a HGS pair located in the upper and lower hexagonal layers, respectively. As shown in a model of architecture, hexagonal bilayered (HBL) Hbs can be built very simply from 144 globin chains and 42 linker chains belonging to two different types. We also propose a simple assembly sequence for the construction of HBL Hbs based on the architecture model.
通过三维投影对齐方法,从分辨率为22埃的冷冻水合蚯蚓血红蛋白(Hb)标本的电子显微镜图像中,对蚯蚓血红蛋白进行了三维重建。采用一种新方法对结果进行分析,该方法考虑了构成三维体积的210个密度随表面表示阈值的变化。具有D6点群对称性的整个寡聚体由12个具有局部三重对称性的中空球状亚结构(HGS)组成,这些亚结构与连接亚基的复杂网络(连接体复合物)相连。每个HGS的12个珠蛋白亚基围绕局部三重轴分布在三层亚基的四层中。最外层的第一层包含单体珠蛋白链2A、3A和5A。对应于其余九个亚基的三个三聚体在第二层(2B、3B、5B)、第三层(1A、4A、6A)和第四层(1B、4B、6B)中各有一个亚基。形成三聚体的珠蛋白链中心之间的距离在20 - 32埃和45 - 52埃范围内。连接体复合物由两种类型的连接单元组成。第一种类型形成连接第二层、第三层和第四层珠蛋白链的三个环。这些亚基的平均分子量(Mm)为25 kDa。第二种类型形成称为六边形环面的中心结构及其与HGS的12个连接。该结构对应于单个连接单元的六聚体,其Mm为(31.2 kDa),大小和形状与HGS环不同。对三维体积结构的仔细研究表明,每个环面连接单元分别与位于上下六边形层的一对HGS的三个环相连。如结构模型所示,六边形双层(HBL)血红蛋白可以非常简单地由属于两种不同类型的144条珠蛋白链和42条连接链构建而成。我们还基于结构模型提出了一种构建HBL血红蛋白的简单组装序列。