The Courant Institute of Mathematical Sciences and the Center for Genomics and Systems Biology, New York University, New York, NY 10003, USA.
J Biomol NMR. 2010 Sep;48(1):31-47. doi: 10.1007/s10858-010-9436-6. Epub 2010 Aug 24.
Methionine residues fulfill a broad range of roles in protein function related to conformational plasticity, ligand binding, and sensing/mediating the effects of oxidative stress. A high degree of internal mobility, intrinsic detection sensitivity of the methyl group, and low copy number have made methionine labeling a popular approach for NMR investigation of selectively labeled protein macromolecules. However, selective labeling approaches are subject to more limited information content. In order to optimize the information available from such studies, we have performed DFT calculations on model systems to evaluate the conformational dependence of (3)J (CSCC), (3)J (CSCH), and the isotropic shielding, sigma(iso). Results have been compared with experimental data reported in the literature, as well as data obtained on [methyl-(13)C]methionine and on model compounds. These studies indicate that relative to oxygen, the presence of the sulfur atom in the coupling pathway results in a significantly smaller coupling constant, (3)J (CSCC)/(3)J (COCC) approximately 0.7. It is further demonstrated that the (3)J (CSCH) coupling constant depends primarily on the subtended CSCH dihedral angle, and secondarily on the CSCC dihedral angle. Comparison of theoretical shielding calculations with the experimental shift range of the methyl group for methionine residues in proteins supports the conclusion that the intra-residue conformationally-dependent shift perturbation is the dominant determinant of delta(13)Cepsilon. Analysis of calmodulin data based on these calculations indicates that several residues adopt non-standard rotamers characterized by very large approximately 100 degrees chi(3) values. The utility of the delta(13)Cepsilon as a basis for estimating the gauche/trans ratio for chi(3) is evaluated, and physical and technical factors that limit the accuracy of both the NMR and crystallographic analyses are discussed.
甲硫氨酸残基在与构象可塑性、配体结合以及感知/介导氧化应激效应相关的蛋白质功能中发挥着广泛的作用。高度的内部流动性、甲基基团的固有检测灵敏度以及低拷贝数使得甲硫氨酸标记成为 NMR 研究选择性标记蛋白质大分子的一种流行方法。然而,选择性标记方法受到更有限的信息含量的限制。为了优化这些研究的可用信息,我们对模型系统进行了 DFT 计算,以评估(3)J(CSCC)、(3)J(CSCH)和各向同性屏蔽,sigma(iso)的构象依赖性。结果与文献中报道的实验数据以及在 [甲基-(13)C]甲硫氨酸和模型化合物上获得的数据进行了比较。这些研究表明,与氧相比,在耦合途径中硫原子的存在导致耦合常数(3)J(CSCC)/(3)J(COCC)显著减小,约为 0.7。进一步证明,(3)J(CSCH)耦合常数主要取决于 CSCH 二面角,其次取决于 CSCC 二面角。与实验位移范围的比较表明,蛋白质中甲硫氨酸残基的理论屏蔽计算支持这样的结论,即构象依赖性位移扰动是(13)Cepsilon 位移的主要决定因素。基于这些计算对钙调蛋白数据的分析表明,几个残基采用了非标准的构象,其特征是非常大的约 100 度 chi(3)值。(13)Cepsilon 作为估计 chi(3)的 gauche/trans 比值的基础的效用进行了评估,并讨论了限制 NMR 和晶体学分析精度的物理和技术因素。