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先天性白内障家系中γD晶体蛋白P23T突变意义的生物信息学分析

Bioinformatics analysis of γD-crystallin protein P23T mutation in a congenital cataract family

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【作者】 董琦郑树徐伟珍蔡善荣姚克

【Author】 DONG Qi~1, ZHENG Shu~1, XU Wei-zhen~1, CAI Shan-rong~1, YAO Ke~2(1. Cancer Institute, The 2~(nd) (Affiliated) Hospital,School of Medicine,Zhejiang University,Hangzhou 310009, China; 2. Department of Ophthalmology, The 2~(nd) Affiliated Hospital,School of Medicine,Zhejiang University,Hangzhou 310009, China)

【机构】 浙江大学医学院附属第二医院肿瘤研究所浙江大学医学院附属第二医院眼科 浙江杭州310009浙江杭州310009浙江杭州310009

【摘要】 本研究前期工作发现在一个遗传性先天性白内障家系中,γD晶体蛋白发生了P23T突变.因此本研究对γD晶体蛋白及其突变体进行了氨基酸序列分析,结构域预测及立体结构模拟等生物信息学研究,以探讨P23T突变对γD晶体蛋白结构与功能的影响.研究结果表明:P23T突变可能影响人γD晶体蛋白与钙离子的结合,导致晶状体内钙离子动态失衡;可以使蛋白分子间形成氢键,降低晶体蛋白溶解度;并使蛋白质表面局部极性的改变,影响蛋白与其它分子的结合.

【Abstract】 A Pro-23→Thr (P23T) substitution in γD-crystallin protein was identified in a hereditary congenital cataract family through previous study. The amino acid sequence, protein domain and motifs, and three-dimension structure of γD-crystallin protein and its mutant were analyzed and predicted. The results showed that the mutation of γD-crystallin protein could affect the ability of the protein to bind itself with calcium ions, thereby inducing dynamic unbalance of the calcium ions in lens. The intermolecular hydrogen-bonds were rearranged, which would reduce the solubility of mutant γD protein. Protein modeling suggests that the effect of this mutation is a subtle one which affect the local polarity of the crystallin molecule surface, and may affect the manner of interaction between γD -crystallin protein and other proteins.

  • 【文献出处】 浙江大学学报(农业与生命科学版) ,Journal of Zhejiang University(Agric.& Life Sci.) , 编辑部邮箱 ,2004年01期
  • 【分类号】R776.1
  • 【被引频次】2
  • 【下载频次】109
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