人类氨基酶N是人类冠状病毒229E的受体
C L Yeager1, R A Ashmun, R K Williams
1Department of Pathology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814-4799.
Nature
|June 4, 1992
概括
人类氨基酶N作为人类冠状病毒229E (HCV-229E) 的受体,促进上呼吸道感染. 这种相互作用是特定的,因为HCV-OC43不利用这种受体.
科学领域:
- 病毒学 病毒学
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
背景情况:
- 人类冠状病毒 (HCV) 是导致上呼吸道感染的重要病原体.
- 两个主要的血清组,HCV-229E和HCV-OC43,负责普通感冒.
研究的目的:
- 为了识别人类冠状病毒菌株HCV-229E.E.的细胞受体.
- 为了调查人类氨基酶N在冠状病毒入境中的作用.
主要方法:
- 利用单克隆抗体RBS阻止HCV-229E感染.
- 进行免疫沉以确定病毒结合伙伴.
- 感染过的小鼠纤维细胞与人类氨基酶N cDNA.
- 在具有不同氨基酶N表达的细胞中评估病毒复制.
主要成果:
- 人类氨基酶N被确定为HCV-229E的特定受体,但不是HCV-OC43.
- 单克隆抗体RBS抑制了HCV-229E感染,免疫降低的氨基酶N,并降低了其酶活性.
- 表达人类氨基酶N的小鼠细胞变得易受HCV-229E感染.
- 氨基酶N的催化不活跃突变未能结合HCV-229E,这表明活性部位参与病毒附着.
结论:
- 人类氨基酶N是HCV-229E的功能性受体.
- 氨基酶N的病毒结合部位可能位于酶的活性部位或附近.
- 这一发现提供了关于HCV-229E进入机制和潜在治疗点的见解.
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