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干扰素在蛋白质合成中的作用特异性。

Specificity of interferon action in protein synthesis.

作者信息

Yau P M, Godefroy-Colburn T, Birge C H, Ramabhadran T V, Thach R E

出版信息

J Virol. 1978 Sep;27(3):648-58. doi: 10.1128/JVI.27.3.648-658.1978.

Abstract

Inhibitors of elongation steps in protein synthesis such as cycloheximide and anisomycin mimic interferon treatment in that they specifically inhibit the synthesis of certain viral proteins. These specific effects are seen only at very low concentrations of the antibiotics, under conditions where host cellular protein synthesis, as well as cell viability, are not severely reduced. A qualitatively as well as quantitatively close correlation between the effects of the two types of agents has been established for encephalomyocarditis virus, vesicular stomatitis virus and murine leukemia virus protein synthesis. It is concluded that one of the primary mechanisms of interferon action may be a nonspecific retardation of one or more elongation steps, and that this may be sufficient to account for its effects on the replication of certain viruses such as encephalomyocarditis and vesicular stomatitis viruses.

摘要

蛋白质合成延伸步骤的抑制剂,如环己酰亚胺和茴香霉素,在特定抑制某些病毒蛋白合成方面模拟了干扰素治疗。这些特定效应仅在抗生素浓度非常低的情况下才能观察到,此时宿主细胞蛋白质合成以及细胞活力并未严重降低。对于脑心肌炎病毒、水疱性口炎病毒和鼠白血病病毒的蛋白质合成,已经确定了这两种类型药物的效应在定性和定量上都密切相关。得出的结论是,干扰素作用的主要机制之一可能是一个或多个延伸步骤的非特异性延迟,并且这可能足以解释其对某些病毒(如脑心肌炎病毒和水疱性口炎病毒)复制的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa13/525853/e4accb6a80d6/jvirol00201-0203-a.jpg

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