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通过核磁共振确定一对互补模块的溶液结构

Solution structure of a pair of complement modules by nuclear magnetic resonance.

作者信息

Barlow P N, Steinkasserer A, Norman D G, Kieffer B, Wiles A P, Sim R B, Campbell I D

机构信息

Department of Biochemistry, University of Oxford, U.K.

出版信息

J Mol Biol. 1993 Jul 5;232(1):268-84. doi: 10.1006/jmbi.1993.1381.

Abstract

A portion of human complement factor H spanning the 15th (H15) and 16th (H16) of its 20 modules, has been expressed in a yeast vector and subjected to structure determination in solution using two-dimensional 1H-NMR. The structure of H15 is very similar to that already established for the fifth module of factor H and H16, consistent with the view that all such complement control (C-) modules share a common overall topology. In addition, the tertiary structures of the component modules of the H15-16 pair are very similar to those of the modules when expressed individually, implying that each folds entirely autonomously within intact factor H. Aromatic residues in the third turn of H15 and the second turn of H16, together with a leucine residue from the linker region, contribute to a small intermodular interface. Comparatively few nuclear Overhauser effects were observable between protons on different modules. Consequently, a wide range of angles of "twist" (131 (+/- 146) degrees, mean value (+/- 1 standard deviation)), i.e. rotation about the long axis of one module with respect to the other, exists in the family of structures generated on the basis of the experimental data. However, much smaller variations occur in the two, orthogonal, angles (175 (+/- 12) degrees and 103 (+/- 6) degrees) that describe the "tilt". These observations may suggest upper limits on the relative flexibility of the two modules. Models were built to assess the outcome of applying such restrictions to all the neighbours within a string of 20 C-modules, and the resulting structures compare well with factor H as visualized by electron microscopy.

摘要

人补体因子H的一部分跨越其20个模块中的第15个(H15)和第16个(H16),已在酵母载体中表达,并使用二维1H-NMR在溶液中进行结构测定。H15的结构与已经确定的因子H第五个模块和H16的结构非常相似,这与所有此类补体控制(C-)模块共享共同整体拓扑结构的观点一致。此外,H15-16对的组成模块的三级结构与单独表达时的模块非常相似,这意味着每个模块在完整的因子H中完全自主折叠。H15第三圈和H16第二圈中的芳香族残基,以及连接区的一个亮氨酸残基,构成了一个小的模块间界面。在不同模块上的质子之间可观察到相对较少的核Overhauser效应。因此,在基于实验数据生成的结构家族中,存在广泛的“扭曲”角度(131(±146)度,平均值(±1标准差)),即一个模块相对于另一个模块绕其长轴的旋转。然而,描述“倾斜”的两个正交角度(175(±12)度和103(±6)度)的变化要小得多。这些观察结果可能暗示了这两个模块相对灵活性的上限。构建了模型来评估对一串20个C-模块内的所有相邻模块应用此类限制的结果,所得结构与电子显微镜观察到的因子H相比非常吻合。

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