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糖基化和葡萄糖修剪抑制剂对人副流感病毒3型的抗病毒作用。

Antiviral effects of glycosylation and glucose trimming inhibitors on human parainfluenza virus type 3.

作者信息

Tanaka Yoshikazu, Kato Junko, Kohara Michinori, Galinski Mark S

机构信息

Department of Veterinary Hygiene, Veterinary School, Nippon Veterinary & Life Science University, 1-7-1 Kyounan, Musashino, Tokyo 180-8602, Japan.

出版信息

Antiviral Res. 2006 Oct;72(1):1-9. doi: 10.1016/j.antiviral.2006.03.016. Epub 2006 May 4.

Abstract

Endoplasmic reticulum (ER) alpha-glucosidase inhibitors block the trimming of N-linked glycosylation and thus prevent the production of several viruses. The present study investigates the antiviral effects of the alpha-glucosidase and alpha-mannosidase inhibitors (castanospermine, 1-deoxynojirimycin, bromoconduritol, deoxymannojirimycin and swainsonine) on human parainfluenza virus type 3 (HPIV3). The alpha-glucosidase inhibitors (castanospermine, 1-deoxynojirimycin) in recombinant expression systems reduced the surface and intracellular expression of both HPIV3 F and HN proteins. On the other hand, alpha-mannosidase inhibitors prevented processing of the oligosaccharides on HPIV3 glycoproteins into the complex form. Consequently, alpha-glycosidase inhibitors (castanospermine and 1-deoxynojirimycin) significantly inhibited viral fusion activity. We demonstrated that the alpha-glucosidase inhibitors (castanospermine and 1-deoxynojirimycin) reduced the infectivity of newly released viral particles. We postulate that alpha-glucosidase inhibitors can prevent the first steps of HPIV3 envelope glycoprotein processing and that the inhibition of glucose trimming has antiviral effects.

摘要

内质网(ER)α-葡萄糖苷酶抑制剂可阻断N-连接糖基化的修剪,从而阻止多种病毒的产生。本研究调查了α-葡萄糖苷酶和α-甘露糖苷酶抑制剂(栗精胺、1-脱氧野尻霉素、溴康唑醇、脱氧甘露野尻霉素和苦马豆素)对3型人副流感病毒(HPIV3)的抗病毒作用。重组表达系统中的α-葡萄糖苷酶抑制剂(栗精胺、1-脱氧野尻霉素)降低了HPIV3 F和HN蛋白的表面和细胞内表达。另一方面,α-甘露糖苷酶抑制剂阻止了HPIV3糖蛋白上的寡糖加工成复杂形式。因此,α-糖苷酶抑制剂(栗精胺和1-脱氧野尻霉素)显著抑制了病毒融合活性。我们证明,α-葡萄糖苷酶抑制剂(栗精胺和1-脱氧野尻霉素)降低了新释放病毒颗粒的感染性。我们推测,α-葡萄糖苷酶抑制剂可以阻止HPIV3包膜糖蛋白加工的第一步,并且对葡萄糖修剪的抑制具有抗病毒作用。

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