Gruber C, Levine S
J Gen Virol. 1983 Apr;64 (Pt 4):825-32. doi: 10.1099/0022-1317-64-4-825.
Four proteins, GP1, VGP48, GP26 and VPM27, are associated with the envelope of respiratory syncytial (RS) virus. The status of GP1 has been uncertain, because a cellular glycoprotein migrates at the same position when Laemmli's discontinuous buffer system is used for PAGE, and because BSC-1 cells infected with the RSN-2 strain of RS virus appear not to contain GP1. However, additional evidence suggests that GP1 is a viral structural protein. (i) It is removed from cells by trypsin, while the cellular glycoprotein is not; (ii) it is separated from the cellular glycoprotein when the infected cells are analysed by neutral SDS-PAGE; (iii) it is present in the purified RSN-2 strain of RS virus produced by BSC-1 cells; (iv) it is also present in the purified Long strain of RS virus produced by either human or monkey cells. When purified Long strain virus is analysed by PAGE under non-reducing conditions, the glycoproteins VGP48 and GP26 migrate together, and VPM27 separates into two proteins, which one-dimensional peptide mapping suggests are not different proteins. These observations suggest that VGP48 and GP26 exist in the virion as a single molecule joined by disulphide bonds, and so resemble a paramyxovirus fusion protein, and that probably there are two forms of VPM27 which differ in either position or number of disulphide bonds.
四种蛋白质,即GP1、VGP48、GP26和VPM27,与呼吸道合胞(RS)病毒的包膜相关。GP1的情况一直不确定,这是因为当使用Laemmli的不连续缓冲系统进行聚丙烯酰胺凝胶电泳(PAGE)时,一种细胞糖蛋白会在相同位置迁移,而且感染RS病毒RSN - 2株的BSC - 1细胞似乎不含GP1。然而,更多证据表明GP1是一种病毒结构蛋白。(i)它可被胰蛋白酶从细胞中去除,而细胞糖蛋白则不会;(ii)当通过中性十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE)分析感染细胞时,它与细胞糖蛋白分离;(iii)它存在于由BSC - 1细胞产生的纯化RSN - 2株RS病毒中;(iv)它也存在于由人或猴细胞产生的纯化的RS病毒Long株中。当在非还原条件下通过PAGE分析纯化的Long株病毒时,糖蛋白VGP48和GP26一起迁移,而VPM27分离成两种蛋白质,一维肽图谱分析表明这两种蛋白质并非不同的蛋白质。这些观察结果表明,VGP48和GP26在病毒粒子中以通过二硫键连接的单个分子形式存在,因此类似于副粘病毒融合蛋白,并且可能存在两种形式的VPM27,它们在二硫键的位置或数量上有所不同。