在HSV-1 ICP0二元域采用了新的β-桶折叠
Erick McCloskey1, Maithri Kashipathy2, Anne Cooper3
1Department of Molecular Biosciences, University of Kansas, Lawrence, Kansas, USA.
Proteins
|February 19, 2024
概括
确定了疹简单病毒1感染细胞蛋白0 (ICP0) C-终端二元域的结构. 这种新型结构对于ICP0在病毒基因调节和复制中的功能至关重要.
科学领域:
- 结构生物学 结构生物学
- 病毒学 病毒学
- 分子生物学分子生物学
背景情况:
- 简单疹病毒1 (HSV-1) 直接早期蛋白质ICP0具有E3无素酶活性.
- ICP0的C端二元域 (残留物555-767) 对于转换病毒基因,病毒复制和从延迟中重新激活至关重要.
- 了解这个域的结构是阐明ICP0功能的关键.
研究的目的:
- 确定HSV-1 ICP0.0的C端二元域的三维结构.
- 调查ICP0的二元化结构基础及其对功能的影响.
主要方法:
- 从细菌中净化ICP0的C端.
- 进行X射线晶体学以解决蛋白质结构.
- 结构数据库搜索和计算分析.
主要成果:
- ICP0二元域由九个β-链和两个α-螺旋组成,每个单体.
- 模聚体的形成涉及β-链的互,创建新的β-桶结构.
- 结晶学数据表明,通过堆叠的β-桶形成了四聚体;折叠是新奇的.
- ICP0可以通过其C终端基因对SUMO1进行二元化或结合,但不能同时进行.
结论:
- ICP0二元域的确定结构是独一无二的.
- 结构洞察力为了解ICP0的监管活动提供了基础.
- 这些知识将有助于更深入地了解HSV-1生命周期.
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