重生病毒细胞附着蛋白具有两个独立活跃的三元化域:主导负面影响的基础
1Department of Microbiology and Infectious Diseases, University of Calgary Health Sciences Center, Alberta, Canada.
Cell
|October 30, 1992
概括
雷奥病毒西格马1蛋白组合涉及独立的N-和C-终端域. N终端启动三元化,促进C终端域的合作折叠以进行细胞附着.
科学领域:
- 病毒学 病毒学
- 结构生物学 结构生物学
- 蛋白质生物化学 蛋白质生物化学
背景情况:
- 复原病毒细胞附着蛋白sigma 1对于病毒进入至关重要.
- 西格玛1是一种同型三元体,具有明显的N端纤维状尾部和C端球状头部域.
研究的目的:
- 阐明reovirus sigma 1蛋白域的独立折叠和三元化机制.
- 为了研究Sigma 1 homotrimer的顺序组装过程.
主要方法:
- 在实验室中对全长和截断的西格玛1蛋白进行协同翻译.
- 蛋白酶敏感性测试用于监测蛋白质折叠和稳定性.
主要成果:
- 西格玛1的N端和C端半端具有独立的三分化和折叠能力.
- N-终端的三元化形成了一种对蛋白酶敏感的卷状线圈,促进C-终端的折叠.
- N端纤维独立成熟成一个稳定的,抗蛋白酶的结构.
结论:
- 西格玛1组件是一个协调的过程,涉及独立的域函数.
- 这种机制突出显示了在寡合蛋白质复合体中突变子单元的主要负面影响.
- 了解西格玛1组合提供了对病毒附着和进入机制的见解.
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