Department of Microbiology and Immunology, College of Veterinary Medicine, China Agricultural University, Beijing 100094, China.
J Biol Chem. 2010 Jul 16;285(29):22505-12. doi: 10.1074/jbc.M109.095000. Epub 2010 May 5.
Three-dimensional structures of beta(2)-microglobulin (beta2m) from chicken and various mammals have been described previously, but aside from genomic sequences, very little is known about the three-dimensional structures of beta2m in species other than warm-blooded vertebrates. Here, we present the first three-dimensional structure of beta2m from bony fish grass carp (Ctid-beta2m), resolved at 2.1 A. The key structural differences between this new structure and previously published structures are two new hydrogen bonds at positions Ile(37) and Glu(38) in strand C and Lys(66) in strand E, and a hydrophobic pocket around the center of the protein found in Ctid-beta2m. Importantly, Ctid-beta2m has a short D strand and a long loop between stands C and D, rather than the flexible region found in other beta2m structures that serves as a putative binding region for the major histocompatibility complex heavy chain. Comparing the Ctid-beta2m structure with those of bovine and human beta2ms, the Calpha root mean square deviation of the latter are 1.3 A and 1.8 A, respectively. Compared with the constant domains of Lamprey T cell receptor-like receptor (Lamp-TCRLC) and Amphioxus V and C domain-bearing protein (Amphi-VCPC), Ctid-beta2m exhibits very different topology. The three-dimensional structures of domains predicted from Amphi-VCPC/Lamp-TCRLC are distinctly lacking in strand A of beta2ms. There are 18 amino acids at the N terminus of Amphi-VCPC that may have evolved into strand A of beta2ms. A mutation in the BC loops of Amphi-VCPC may have led to the novel topology found in beta2m. Based on these results, Ctid-beta2m may well reflect evolutionary characteristics of ancestral C set molecules.
先前已经描述了来自鸡和各种哺乳动物的β2-微球蛋白(β2m)的三维结构,但除了基因组序列外,对于除温血脊椎动物以外的物种的β2m 的三维结构知之甚少。在这里,我们首次呈现来自硬骨鱼草鱼(Ctid-β2m)的β2m 的三维结构,分辨率为 2.1Å。该新结构与先前发表的结构之间的关键结构差异在于在 C 链上的位置 Ile(37)和 Glu(38)以及 E 链上的 Lys(66)处形成两个新的氢键,并且在 Ctid-β2m 中发现的蛋白质的中心周围存在一个疏水性口袋。重要的是,Ctid-β2m 具有短的 D 链和 C 与 D 之间的长环,而不是其他 β2m 结构中发现的柔性区域,该柔性区域充当主要组织相容性复合物重链的潜在结合区域。将 Ctid-β2m 结构与牛和人β2m 进行比较,后者的 Calpha 均方根偏差分别为 1.3Å和 1.8Å。与七鳃鳗 T 细胞受体样受体(Lamp-TCRLC)和文昌鱼 V 和 C 结构域携带蛋白(Amphi-VCPC)的恒定结构域相比,Ctid-β2m 表现出非常不同的拓扑结构。从 Amphi-VCPC/Lamp-TCRLC 预测的结构域的三维结构明显缺乏β2m 的 A 链。Amphi-VCPC 的 N 端有 18 个氨基酸可能已经进化为β2m 的 A 链。Amphi-VCPC 的 BC 环中的突变可能导致了β2m 中发现的新拓扑结构。基于这些结果,Ctid-β2m 很可能反映了祖先 C 集合分子的进化特征。