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双异丙氧乙酰胺(WIN 51711)对脊髓灰质炎病毒脱壳的抑制作用。

Inhibition of poliovirus uncoating by disoxaril (WIN 51711).

作者信息

Zeichhardt H, Otto M J, McKinlay M A, Willingmann P, Habermehl K O

出版信息

Virology. 1987 Sep;160(1):281-5. doi: 10.1016/0042-6822(87)90075-4.

Abstract

Disoxaril [WIN 51711, 5-[7-[4(4,5-dihydro-2-oxazolyl)phenoxy]heptyl]-3- methylisoxazole] inhibits the replication of polioviruses types 1 and 2 in HeLa cells by stabilizing the virus capsid, which results in the inhibition of the pH-dependent viral uncoating in endosomes and/or lysosomes. As shown by electron microscopy the virus entered into the cell by receptor-mediated endocytosis via coated pits and coated vesicles into endosomes irrespective of the presence or absence of the compound. Measurements of viral RNA synthesis showed that disoxaril completely inhibited the arrival of viral RNA in the cytoplasm for new RNA synthesis only when the inocula were preincubated with disoxaril for 15 min at 37 degrees at 0.3 microgram disoxaril/ml for poliovirus type 1 and 0.03 microgram disoxaril/ml for poliovirus type 2. Simultaneous addition of the compound and virus resulted in reduced inhibition of viral RNA synthesis. The inhibitory effect of the compound could be partially reversed up to 25 min p.i. if the compound was eluted from the cells.

摘要

双氯苯咪唑[WIN 51711,5-[7-[4-(4,5-二氢-2-恶唑基)苯氧基]庚基]-3-甲基异恶唑]通过稳定病毒衣壳抑制脊髓灰质炎病毒1型和2型在HeLa细胞中的复制,这导致在内体和/或溶酶体中依赖pH的病毒脱壳受到抑制。电子显微镜显示,无论是否存在该化合物,病毒均通过受体介导的内吞作用,经有被小窝和有被小泡进入内体而进入细胞。病毒RNA合成的测量结果表明,仅当接种物在37℃下用双氯苯咪唑预孵育15分钟时,双氯苯咪唑才会完全抑制病毒RNA到达细胞质以进行新的RNA合成,其中脊髓灰质炎病毒1型的双氯苯咪唑浓度为0.3微克/毫升,脊髓灰质炎病毒2型的双氯苯咪唑浓度为0.03微克/毫升。同时加入该化合物和病毒会导致病毒RNA合成的抑制作用减弱。如果该化合物从细胞中洗脱,其抑制作用在感染后25分钟内可部分逆转。

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