Trybala E, Bergström T, Spillmann D, Svennerholm B, Olofsson S, Flynn S J, Ryan P
Department of Clinical Virology, University of Göteborg, Guldhedsgatan 10B, Göteborg, 413 46, Sweden.
Virology. 1996 Apr 1;218(1):35-42. doi: 10.1006/viro.1996.0163.
It has been demonstrated that the efficient attachment of pseudorabies virus (PrV) is mediated by an interaction between glycoprotein C (gC) and a cellular heparin-like substance (T. C. Mettenleiter, L. Zsak, F. Zuckermann, N. Sugg, H. Kern, and t. Ben-Porat, J. Virol. 64, 278-286, 1990). According to the prevalent concept, this interaction is likely to occur between clusters of basic residues of PrV gC and the negatively charged sulfate esters and carboxylate groups of heparan sulfate/heparin. To elucidate which of the three major types of sulfate groups of heparan sulfate/heparin are involved in the interaction with PrV, we used selectively N-, 2-O-, and 6-O-desulfated samples and other modified heparins as competitors in virus-attachment assays. PrV exhibited limited preference for the specific sulfate groups of heparan sulfate/heparin in accordance with a hierarchy of 6-O- > 2-O- > N-sulfates. In addition, since selective removal of any of the specific sulfates had only a slight effect on the competition capacity of heparin, it is likely that the combination of any two of three types of sulfate groups could contribute to an interaction with PrV with an efficiency nearly equal to native, fully sulfated heparin. When tested on different cell lines the pattern of PrV requirement for the specific O-sulfate groups, i.e., 6-O-sulfates > 2-O-sulfates, remained the same. However, different minimum lengths of heparin fragments were required to inhibit PrV attachment to different cell lines, suggesting a relative virus flexibility in accommodation to different forms of heparan sulfate.
已证明伪狂犬病病毒(PrV)的有效附着是由糖蛋白C(gC)与细胞类肝素物质之间的相互作用介导的(T.C.梅滕莱特、L.扎克、F.祖克曼、N.萨格、H.克恩和T.本-波拉特,《病毒学杂志》64卷,278 - 286页,1990年)。根据普遍观点,这种相互作用可能发生在PrV gC的碱性残基簇与硫酸乙酰肝素/肝素带负电荷的硫酸酯和羧基之间。为了阐明硫酸乙酰肝素/肝素的三种主要硫酸基团类型中哪一种参与了与PrV的相互作用,我们使用了选择性N -、2 - O -和6 - O -去硫酸化样品以及其他修饰的肝素作为病毒附着试验中的竞争者。PrV对硫酸乙酰肝素/肝素的特定硫酸基团表现出有限的偏好,其偏好顺序为6 - O - > 2 - O - > N -硫酸酯。此外,由于选择性去除任何一种特定的硫酸盐对肝素的竞争能力只有轻微影响,很可能三种类型的硫酸基团中任意两种的组合都能以几乎与天然的、完全硫酸化的肝素相等的效率与PrV发生相互作用。当在不同细胞系上进行测试时,PrV对特定O -硫酸基团(即6 - O -硫酸盐> 2 - O -硫酸盐)的需求模式保持不变。然而,抑制PrV附着到不同细胞系所需的肝素片段的最小长度不同,这表明病毒在适应不同形式的硫酸乙酰肝素方面具有相对的灵活性。