Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi 75270, Pakistan.
Eur Biophys J. 2011 Jun;40(6):715-26. doi: 10.1007/s00249-011-0684-5. Epub 2011 Mar 1.
A molecular dynamics simulation study of mononuclear iron 15S-lipoxygenase (15S-LOX) from rabbit reticulocytes was performed to investigate its structure and dynamics; newly developed AMBER force field parameters were employed for the first coordination sphere of the catalytic iron (II). The results obtained from this study demonstrate that the structural features of the catalytic iron coordination site are in good agreement with available data obtained from experiments. The motional flexibility of the N-terminal β-barrel domain is greater than the C-terminal catalytic domain; flexibility was assessed in terms of B-factors and secondary structure calculations. The significant features obtained for the relative motional flexibility of these two domains of 15S-LOX in solution as well as the isolated C-terminal domain were analyzed in terms of radius of gyration and maximum diameter, which correlated well with the structural flexibility of 15-lipoxygenase-1 in solution as probed by small-angle X-ray scattering. The motional flexibility indicates interdomain motion between the N-terminal β-barrel and the C-terminal catalytic domain; this was further verified by the evaluation of central bending in the solvated LOX molecule, which identified an unstructured stretch of amino acids as the interdomain linker. The average bending angle confirmed significant central bending between these two domains, which was linked to the high degree of motional freedom of the N-terminal β-barrel domain in aqueous solutions. This can be considered to have biological relevance for membrane binding as well as for regulating the catalytic domain.
采用新开发的 AMBER 力场参数对兔网织红细胞单核铁 15S-脂氧合酶(15S-LOX)进行了分子动力学模拟研究,以研究其结构和动力学;首次对催化铁(II)的第一配位球进行了研究。该研究结果表明,催化铁配位位点的结构特征与实验获得的现有数据非常吻合。N 端β-桶结构域的运动灵活性大于 C 端催化结构域;通过 B 因子和二级结构计算来评估灵活性。对 15S-LOX 在溶液中以及分离的 C 端结构域的这两个结构域的相对运动灵活性的重要特征进行了分析,其分析指标为旋转半径和最大直径,这些特征与小角度 X 射线散射探测到的溶液中 15-脂氧合酶-1 的结构灵活性密切相关。运动灵活性表明 N 端β-桶和 C 端催化结构域之间存在结构域间运动;通过对溶剂化 LOX 分子的中心弯曲进行评估,进一步验证了这种结构域间运动,该评估确定了无规则伸展的氨基酸作为结构域间的连接物。平均弯曲角度证实了这两个结构域之间存在显著的中心弯曲,这与水溶液中 N 端β-桶结构域的高运动自由度有关。这可以被认为与膜结合以及调节催化结构域具有生物学相关性。