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The measurement and prediction of electric fields in the active site of human aldose reductase.

机译:人醛糖还原酶活性位点中电场的测量和预测。

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The electric potentials and fields produced by the organization of charged and polar groups in folded proteins influence nearly every aspect of protein function. While a large number of computational techniques have been developed to estimate potentials and fields in proteins relatively few experiments measure quantities directly related to these calculations. Vibrational spectroscopy is used to measure changes in field due to mutation in an enzyme's active site. The sensitivity of various bond types to electric fields is calibrated by observing the change in the infrared absorption spectra of immobilized samples upon application of an external electric field. The nitrile vibration is identified as the most general probe due to its ideal frequency, relatively large intensity and sensitivity to electric fields. Several methods of incorporating nitriles into proteins are explored and infrared spectra of nitrile containing proteins are presented.; To investigate electric fields in the active site human aldose reductase the nitrile containing inhibitor IDD743 is used. The sensitivity IDD743's nitrile stretching frequency to electric fields is determined and absorption spectra are obtained for the inhibitor bound to wild-type and several mutants. From the calibrated sensitivity and the observed frequency shifts the change in field along IDD743's nitrile for these mutations is determined. The experimentally determined fields are compared to those predicted by continuum electrostatics calculations. It is found that the calculated fields are extremely sensitive to the side chain conformation selected for mutant structures. Molecular mechanics simulations are used to relax side chain conformations from initial models and continuum electrostatic calculations are performed along these trajectories. Distributions of field for wild-type and mutants are calculated for trajectories at long time. It is argued that these distributions provide a much better description of the experimentally determined changes in field than electrostatics calculations performed on single static structures.
机译:折叠蛋白质中带电和极性基团的组织产生的电势和电场几乎影响蛋白质功能的各个方面。尽管已经开发出许多计算技术来估计蛋白质中的潜力和领域,但很少有实验测量与这些计算直接相关的量。振动光谱法用于测量由于酶活性位点突变引起的视野变化。通过观察施加外电场后固定样品的红外吸收光谱的变化,可以校准各种键类型对电场的敏感性。腈振动由于其理想的频率,相对较大的强度和对电场的敏感性而被认为是最通用的探头。探索了几种将腈掺入蛋白质的方法,并给出了含腈蛋白质的红外光谱。为了研究活性位点人醛糖还原酶中的电场,使用了含腈的抑制剂IDD743。确定了IDD743对电场的腈拉伸频率的敏感性,并获得了与野生型和几个突变体结合的抑制剂的吸收光谱。根据校准的灵敏度和观察到的频率偏移,可以确定这些突变沿IDD743腈方向的场变化。将实验确定的场与通过连续静电学计算预测的场进行比较。发现所计算的场对为突变结构选择的侧链构象极为敏感。分子力学模拟用于从初始模型中放宽侧链构象,并沿着这些轨迹进行连续静电计算。计算长时间内轨迹的野生型和突变体的场分布。有人认为,与对单个静态结构执行的静电计算相比,这些分布提供了对实验确定的电场变化的更好描述。

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