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From the Cover: X-ray damage to the Mn4Ca complex in single crystals of photosystem II: A case study for metalloprotein crystallography

机译:从封面开始:X射线对光系统II单晶中Mn4Ca络合物的破坏:金属蛋白晶体学的案例研究

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摘要

X-ray absorption spectroscopy was used to measure the damage caused by exposure to x-rays to the Mn4Ca active site in single crystals of photosystem II as a function of dose and energy of x-rays, temperature, and time. These studies reveal that the conditions used for structure determination by x-ray crystallography cause serious damage specifically to the metal-site structure. The x-ray absorption spectra show that the structure changes from one that is characteristic of a high-valent Mn4(III2,IV2) oxo-bridged Mn4Ca cluster to that of Mn(II) in aqueous solution. This damage to the metal site occurs at a dose that is more than one order of magnitude lower than the dose that results in loss of diffractivity and is commonly considered safe for protein crystallography. These results establish quantitative x-ray dose parameters that are applicable to redox-active metalloproteins. This case study shows that a careful evaluation of the structural intactness of the active site(s) by spectroscopic techniques can validate structures derived from crystallography and that it can be a valuable complementary method before structure–function correlations of metalloproteins can be made on the basis of high-resolution x-ray crystal structures.
机译:X射线吸收光谱法用于测量光系统II单晶中Mn4Ca活性位点暴露于X射线所引起的损害,该损害是X射线的剂量和能量,温度和时间的函数。这些研究表明,用于通过X射线晶体学确定结构的条件特别是严重破坏了金属位点结构。 X射线吸收光谱表明,该结构从高价Mn4(III2,IV2)氧桥联Mn4Ca簇的特征结构转变为水溶液中的Mn(II)结构。对金属部位的这种损害的剂量比导致衍射损失的剂量低一个数量级以上,并且通常被认为对蛋白质晶体学是安全的。这些结果建立了适用于氧化还原活性金属蛋白的定量X射线剂量参数。该案例研究表明,通过光谱技术仔细评估活性位点的结构完整性可以验证晶体学衍生的结构,并且在基于金属蛋白进行结构-功能相关性分析之前,它可以作为有价值的补充方法。 x射线晶体的高分辨率结构。

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