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Photoinduced transport in an H64Q neuroglobin antidote for carbon monoxide poisoning

机译:用于一氧化碳中毒的H64Q神经胶蛋白解毒剂中的光诱导

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Carbon monoxide (CO) is a leading cause of poisoning deaths worldwide, without available antidotal therapy. Recently, a potential treatment for CO poisoning was introduced, based on binding of CO by neuroglobin (Ngb) with a mutated distal histidine (H64Q). Here, we present an atomistic mechanism of CO trapping by H64Q Ngb revealed by nonadiabatic molecular dynamics. We focused on CO photodissociation and recombination of CO to wild type (WT) and H64QNgb. Our results demonstrate that the distribution of CO within the proteins differs substantially due to rearrangement of amino acids surrounding the distal heme pocket. This leads to the decrease of the distal pocket volume in H64Q Ngb in comparison to WT Ngb, trapping migrating CO molecules in the distal pocket. We show that the mutation implicates the shortening of the time scale of CO geminate recombination, making H64Q Ngb 2.7 times more frequent binder than WT Ngb. Published by AIP Publishing.
机译:一氧化碳(CO)是全世界死亡死亡的主要原因,无需可用的抗鱼疗法。 最近,基于CO通过突变的远端组氨酸(H64Q)的CO通过CO的结合引入了对CO中毒的潜在处理。 在这里,我们介绍了由非等级分子动力学揭示的H64Q NGB Co诱捕的原子学机制。 我们专注于Co Photodissociation和Co的重组至野生型(WT)和H64QNGB。 我们的结果表明,蛋白质内的CO的分布基本上不同,因为重排围绕远端血红素袋的氨基酸。 与WT NGB相比,这导致H64Q NGB中远端口袋体积的降低,捕获远端口袋中的迁移CO分子。 我们表明,该突变暗示了Co Geminate重组的时间量表的缩短,使H64Q NGB的2.7倍比Wt NGB更频繁。 通过AIP发布发布。

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