Yao Yong, Bhabha Gira, Kroon Gerard, Landes Mindy, Dyson H Jane
Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
J Biomol NMR. 2008 Jan;40(1):23-30. doi: 10.1007/s10858-007-9207-1. Epub 2007 Nov 28.
NMR measurements can give important information on solution structure, without the necessity for a full-scale solution structure determination. The C-terminal protein binding domain of the ribosome-associated chaperone protein trigger factor is composed of non-contiguous parts of the polypeptide chain, with an interpolated prolyl isomerase domain. A construct of the C-terminal domain of Escherichia coli trigger factor containing residues 113-149 and 247-432, joined by a Gly-Ser-Gly-Ser linker, is well folded and gives excellent NMR spectra in solution. We have used NMR measurements on this construct, and on a longer construct that includes the prolyl isomerase domain, to distinguish between two possible structures for the C-terminal domain of trigger factor, and to assess the behavior of the trigger factor C-terminal domain in solution. Two X-ray crystal structures, of intact trigger factor from E. coli (Ferbitz et al., Nature 431:590-596, 2004), and of a truncated trigger factor from Vibrio cholerae (Ludlam et al., Proc Natl Acad Sci USA 101:13436-13441, 2004) showed significant differences in the structure of the C-terminal domain, such that the two structures could not be superimposed. We show using NMR chemical shifts and long range nuclear Overhauser effects that the secondary and tertiary structure of the E. coli C-terminal domain in solution is consistent with the crystal structure of the E. coli trigger factor and not with the V. cholerae protein. Given the similarity of the amino acid sequences of the E. coli and V. cholerae proteins, it appears likely that the structure of the V. cholerae protein has been distorted as a result of truncation of a 44-amino acid segment at the C-terminus. Analysis of residual dipolar coupling measurements shows that the overall topology of the solution structure is completely inconsistent with both structures. Dynamics analysis of the C-terminal domain using T1, T2 and heteronuclear NOE parameters show that the protein is overall rather flexible. These results indicate that the structure of this domain in solution resembles the X-ray crystal structure of the E. coli protein in secondary structure and at least some tertiary contacts, but that the overall topology differs in solution, probably due to structural fluctuation.
核磁共振(NMR)测量可以提供有关溶液结构的重要信息,而无需进行全面的溶液结构测定。核糖体相关伴侣蛋白触发因子的C末端蛋白结合结构域由多肽链的不连续部分组成,并插入了一个脯氨酰异构酶结构域。一种大肠杆菌触发因子C末端结构域的构建体,包含残基113 - 149和247 - 432,通过甘氨酸 - 丝氨酸 - 甘氨酸 - 丝氨酸接头连接,折叠良好,并在溶液中给出出色的NMR谱图。我们对该构建体以及包含脯氨酰异构酶结构域的更长构建体进行了NMR测量,以区分触发因子C末端结构域的两种可能结构,并评估触发因子C末端结构域在溶液中的行为。来自大肠杆菌的完整触发因子(Ferbitz等人,《自然》431:590 - 596,2004)和来自霍乱弧菌的截短触发因子(Ludlam等人,《美国国家科学院院刊》101:13436 - 13441,2004)的两个X射线晶体结构显示,C末端结构域的结构存在显著差异,以至于这两个结构无法叠加。我们利用NMR化学位移和长程核Overhauser效应表明,溶液中大肠杆菌C末端结构域的二级和三级结构与大肠杆菌触发因子的晶体结构一致,而与霍乱弧菌蛋白的晶体结构不一致。鉴于大肠杆菌和霍乱弧菌蛋白氨基酸序列的相似性,霍乱弧菌蛋白的结构似乎因C末端44个氨基酸片段的截短而发生了扭曲。残余偶极耦合测量分析表明,溶液结构的整体拓扑与这两种结构都完全不一致。使用T1、T2和异核NOE参数对C末端结构域进行动力学分析表明,该蛋白总体上相当灵活。这些结果表明,该结构域在溶液中的结构在二级结构和至少一些三级接触方面类似于大肠杆菌蛋白的X射线晶体结构,但在溶液中的整体拓扑不同,可能是由于结构波动所致。