肌病相关突变体FHL1在水中的分子动力学模拟及结构稳定性分析

H. Takeuchi, H. Okajima, H. Itoga, K. Nobuoka, Hironao Yamada, T. Miyakawa, R. Morikawa, Y. Hayashi, M. Takasu
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摘要

FHL1基因的突变可引起x连锁遗传性肌病,这是一种罕见的顽固性疾病。从婴儿期早期到成年期,发病年龄变化很大,患者表现为进行性肌肉无力和萎缩。FHL1蛋白由四个半LIM结构域组成。每个LIM结构域包含两个锌指,这有助于LIM结构域的结构稳定性。第二LIM结构域(LIM2)中半胱氨酸或组氨酸残基的改变与疾病严重程度密切相关。因此,我们认为LIM2在维持FHL1的结构中起着重要的作用。本研究对野生型和突变型FHL1的LIM1和LIM2组成的分子模型进行了分子动力学模拟。计算了锌指结构的变形程度,测量了锌配位残基中锌原子与Cα原子之间的距离。我们的分析表明,在与严重肌病相关的突变体中,这两个数量之间的相关性更大。FHL1基因的突变可引起x连锁遗传性肌病,这是一种罕见的顽固性疾病。从婴儿期早期到成年期,发病年龄变化很大,患者表现为进行性肌肉无力和萎缩。FHL1蛋白由四个半LIM结构域组成。每个LIM结构域包含两个锌指,这有助于LIM结构域的结构稳定性。第二LIM结构域(LIM2)中半胱氨酸或组氨酸残基的改变与疾病严重程度密切相关。因此,我们认为LIM2在维持FHL1的结构中起着重要的作用。本研究对野生型和突变型FHL1的LIM1和LIM2组成的分子模型进行了分子动力学模拟。计算了锌指结构的变形程度,测量了锌配位残基中锌原子与Cα原子之间的距离。我们的分析表明,这两个量之间的相关性在…
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Molecular dynamics simulation of myopathy-related mutant FHL1 in water and analysis of structure stabilization
Mutations in the FHL1 gene can cause X-linked hereditary myopathy, which causes one of the rarest intractable diseases. The age of the disease onset is quite variable from early infancy to adulthood, and the patients show progressive muscle weakness and atrophy. The FHL1 protein is constituted by four and a half LIM domains. Each LIM domain contains two zinc fingers, which contribute to the structural stability of the LIM domain. A change in the cysteine or histidine residues in the 2nd LIM domain (LIM2) is closely associated with the disease severity. Therefore, LIM2 is suggested to have an essential role in maintaining the structure of FHL1. In this study, molecular dynamics simulation was performed on molecular models consisting of LIM1 and LIM2 of wild and mutant FHL1. We calculated the extent of distortion of zinc finger structure and measured the distance between zinc atom and Cα atom of zinc-coordinated residues. Our analysis showed that the correlation between these two quantities is larger in the mutants associated with severe myopathy.Mutations in the FHL1 gene can cause X-linked hereditary myopathy, which causes one of the rarest intractable diseases. The age of the disease onset is quite variable from early infancy to adulthood, and the patients show progressive muscle weakness and atrophy. The FHL1 protein is constituted by four and a half LIM domains. Each LIM domain contains two zinc fingers, which contribute to the structural stability of the LIM domain. A change in the cysteine or histidine residues in the 2nd LIM domain (LIM2) is closely associated with the disease severity. Therefore, LIM2 is suggested to have an essential role in maintaining the structure of FHL1. In this study, molecular dynamics simulation was performed on molecular models consisting of LIM1 and LIM2 of wild and mutant FHL1. We calculated the extent of distortion of zinc finger structure and measured the distance between zinc atom and Cα atom of zinc-coordinated residues. Our analysis showed that the correlation between these two quantities is larger in the...
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