Schlesinger S, Koyama A H, Malfer C, Gee S L, Schlesinger M J
Virus Res. 1985 Mar;2(2):139-49. doi: 10.1016/0168-1702(85)90244-8.
We have examined the effects of deoxynojirimycin and castanospermine, compounds known to inhibit the removal of glucose from high mannose asparagine-linked oligosaccharides, on the formation of Sindbis virus. These drugs inhibited virion formation in baby hamster kidney (BHK) cells, 15B - the CHO cell line that lacks GlcNAc transferase activity, and chicken embryo fibroblasts, although our results with the latter cells were variable. We analyzed the [3H]mannose-labeled oligosaccharides from Sindbis virus infected 15B cells. Those from control cells were predominantly GlcNAc2Man5. Oligosaccharides from the treated cells were larger than the Man5 species and as expected, were partially resistant to alpha-mannosidase. The growth of Sindbis virus was inhibited to a much greater extent at 37 degrees C than at 30 degrees C in BHK cells treated with either deoxynojirimycin or castanospermine. Both of these compounds also inhibited the proteolytic cleavage of the viral glycoprotein precursor, PE2, to the virion glycoprotein, E2, but did not prevent the migration of the glycoprotein to the cell surface. These results, taken together with our earlier studies with vesicular stomatitis virus (Schlesinger et al., 1984) provide strong evidence that the removal of glucose residues during the processing of asparagine-linked oligosaccharides is critical for some proteins to achieve a functional conformation.
我们研究了脱氧野尻霉素和栗精胺(已知可抑制从高甘露糖型天冬酰胺连接的寡糖中去除葡萄糖的化合物)对辛德毕斯病毒形成的影响。这些药物抑制了幼仓鼠肾(BHK)细胞、缺乏N-乙酰葡糖胺转移酶活性的CHO细胞系15B以及鸡胚成纤维细胞中病毒粒子的形成,不过我们对后一种细胞的研究结果并不稳定。我们分析了来自感染辛德毕斯病毒的15B细胞的[3H]甘露糖标记的寡糖。对照细胞的寡糖主要是GlcNAc2Man5。处理过的细胞中的寡糖比Man5种类更大,并且正如预期的那样,对α-甘露糖苷酶有部分抗性。在用脱氧野尻霉素或栗精胺处理的BHK细胞中,辛德毕斯病毒在37℃时的生长比在30℃时受到的抑制程度要大得多。这两种化合物还抑制了病毒糖蛋白前体PE2向病毒粒子糖蛋白E2的蛋白水解切割,但并未阻止糖蛋白向细胞表面的迁移。这些结果与我们早期对水泡性口炎病毒的研究(施莱辛格等人,1984年)相结合,提供了有力证据,表明在天冬酰胺连接的寡糖加工过程中去除葡萄糖残基对于某些蛋白质形成功能构象至关重要。