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Atomic model of the F420-reducing NiFe hydrogenase by electron cryo-microscopy using a direct electron detector

机译:F420还原NiFe氢化酶的原子模型通过使用直接电子检测器的电子冷冻显微镜观察

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摘要

The introduction of direct electron detectors with higher detective quantum efficiency and fast read-out marks the beginning of a new era in electron cryo-microscopy. Using the FEI Falcon II direct electron detector in video mode, we have reconstructed a map at 3.36 Å resolution of the 1.2 MDa F420-reducing hydrogenase (Frh) from methanogenic archaea from only 320,000 asymmetric units. Videos frames were aligned by a combination of image and particle alignment procedures to overcome the effects of beam-induced motion. The reconstructed density map shows all secondary structure as well as clear side chain densities for most residues. The full coordination of all cofactors in the electron transfer chain (a [NiFe] center, four [4Fe4S] clusters and an FAD) is clearly visible along with a well-defined substrate access channel. From the rigidity of the complex we conclude that catalysis is diffusion-limited and does not depend on protein flexibility or conformational changes.>DOI:
机译:具有更高检测量子效率和快速读出功能的直接电子检测器的推出标志着电子冷冻显微镜新时代的开始。使用视频模式下的FEI Falcon II直接电子探测器,我们仅从320,000个不对称单元中就从产甲烷菌中提取了1.2 MDa F420还原氢酶(Frh),分辨率为3.36Å。通过图像和粒子对齐程序的组合来对齐视频帧,以克服光束引起的运动的影响。重建的密度图显示了大多数残基的所有二级结构以及清晰的侧链密度。电子转移链中所有辅因子([NiFe]中心,四个[4Fe4S]簇和一个FAD)的完全配位以及定义明确的底物进入通道清晰可见。从复合物的刚度可以得出结论,催化是受扩散限制的,并且不取决于蛋白质的柔韧性或构象变化。> DOI:

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