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Comment on 'On the Functional Annotation of Open-Channel Structures in the Glycine Receptor'' Comment

机译:浅谈“甘氨酸受体中开放通道结构的功能注释”

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摘要

Recently, we reported the simulation of a stable open state of the glycine receptor. Central to the stability of the simulations was the behavior of the highly conserved leucine residues at the 90 gate, which were found to rotate into adjacent pockets, thus providing a structural rationale for decades of biochemical observations. In contrast, a previously reported model from Cerdan et al. (2018) resembled a more collapsed state. However, in support of their model, they draw attention to the agreement between calculated and experimental conductance measurements and argue that our model tends to overestimate ion flow. Here, we argue that there are many pitfalls with this approach and that the apparent agreement most likely reflects a fortuitous cancellation of errors. The computed values are highly sensitive to very small changes in model parameters. It is also likely that polarization effects will be very significant, and these have not yet been considered.
机译:最近,我们报道了甘氨酸受体稳定的开放状态的模拟。 模拟稳定性的核心是90栅极的高度保守亮氨酸残基的行为,该残留在90浇口中被发现旋转到相邻的口袋中,从而提供数十年的生物化学观测的结构理由。 相比之下,来自Cerdan等人的先前报告的模型。 (2018)类似于更崩溃的状态。 然而,为了支持其模型,他们提请注意计算和实验导电测量之间的协议,并认为我们的模型倾向于高估离子流量。 在这里,我们认为这种方法存在许多陷阱,并且表观协议最有可能反映出偶然的错误取消。 计算值对模型参数的非常小的变化非常敏感。 极化效应也很可能是非常重要的,这些效果尚未考虑。

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  • 来源
    《Structure》 |2020年第6期|共3页
  • 作者单位

    Univ Oxford Dept Biochem Struct Bioinformat &

    Computat Biochem South Parks Rd Oxford OX1 3QU England;

    Univ Oxford Dept Biochem Struct Bioinformat &

    Computat Biochem South Parks Rd Oxford OX1 3QU England;

    Univ Oxford Dept Biochem Struct Bioinformat &

    Computat Biochem South Parks Rd Oxford OX1 3QU England;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子生物学;
  • 关键词

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