Eck M J, Sprang S R
Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas 95235-9050.
J Biol Chem. 1989 Oct 15;264(29):17595-605. doi: 10.2210/pdb1tnf/pdb.
The three-dimensional structure of tumor necrosis factor (TNF-alpha), a protein hormone secreted by macrophages, has been determined at 2.6 A resolution by x-ray crystallography. Phases were determined by multiple isomorphous replacement using data collected from five heavy atom derivatives. The multiple isomorphous replacement phases were further improved by real space symmetry averaging, exploiting the noncrystallographic 3-fold symmetry of the TNF-alpha trimer. An atomic model corresponding to the known amino acid sequence of TNF-alpha was readily built into the electron density map calculated with these improved phases. The 17,350-dalton monomer forms an elongated, antiparallel beta-pleated sheet sandwich with a "jelly-roll" topology. Three monomers associate intimately about a 3-fold axis of symmetry to form a compact bell-shaped trimer. Examination of the model and comparison to known protein structures reveals striking structural homology to several viral coat proteins, particularly satellite tobacco necrosis virus. Locations of residues conserved between TNF-alpha and lymphotoxin (TNF-beta, a related cytokine known to bind to the same receptors as TNF-alpha) suggest that lymphotoxin, like TNF-alpha, binds to the receptor as a trimer and that the general site of interaction with the receptor is at the "base" of the trimer.
肿瘤坏死因子(TNF-α)是巨噬细胞分泌的一种蛋白质激素,其三维结构已通过X射线晶体学在2.6埃分辨率下确定。通过对从五种重原子衍生物收集的数据进行多同晶置换来确定相位。利用TNF-α三聚体的非晶体学3重对称性,通过实空间对称平均进一步改善多同晶置换相位。与TNF-α已知氨基酸序列相对应的原子模型很容易构建到用这些改进相位计算出的电子密度图中。17350道尔顿的单体形成一个具有“果冻卷”拓扑结构的细长反平行β折叠片层夹心结构。三个单体围绕一个3重对称轴紧密结合形成一个紧凑的钟形三聚体。对该模型的检查以及与已知蛋白质结构的比较揭示了与几种病毒外壳蛋白惊人的结构同源性,特别是卫星烟草坏死病毒。TNF-α和淋巴毒素(TNF-β,一种已知与TNF-α结合相同受体的相关细胞因子)之间保守残基的位置表明,淋巴毒素与TNF-α一样,以三聚体形式与受体结合,并且与受体相互作用的一般位点在三聚体的“底部”。