Isola V J, Eisenberg R J, Siebert G R, Heilman C J, Wilcox W C, Cohen G H
Department of Microbiology, School of Dental Medicine, University of Pennsylvania, Philadelphia 19104.
J Virol. 1989 May;63(5):2325-34. doi: 10.1128/JVI.63.5.2325-2334.1989.
Glycoprotein D (gD) is a virion envelope component of herpes simplex virus types 1 (HSV-1) and 2 (HSV-2) which plays an important role in viral infection and pathogenesis. Previously, anti-gD monoclonal antibodies (MAbs) were arranged into groups which recognize distinct type-common and type-specific sites on HSV-1 gD (gD-1) and HSV-2 gD (gD-2). Several groups recognize discontinuous epitopes which are dependent on tertiary structure. Three groups, VII, II, and V, recognize continuous epitopes present in both native and denatured gD. Previously, group II consisted of a single MAb, DL6, whose epitope was localized between amino acids 268 and 287. In the study reported here, we extended our analysis of the antigenic structure of gD, concentrating on continuous epitopes. The DL6 epitope was localized with greater precision to residues 272 to 279. Four additional MAbs including BD78 were identified, each of which recognizes an epitope within residues 264 to 275. BD78 and DL6 blocked each other in binding to gD. In addition, a mutant form of gD was constructed in which the proline at 273 was replaced by serine. This change removes a predicted beta turn in gD. Neither antibody reacted with this mutant, indicating that the BD78 and DL6 epitopes overlap and constitute an antigenic site (site II) within residues 264 to 279. A separate antigenic site (site XI) was recognized by MAb BD66 (residues 284 to 301). This site was only six amino acids downstream of site II, but was distinct as demonstrated by blocking studies. Synthetic peptides mimicking these and other regions of gD were screened with polyclonal antisera to native gD-1 or gD-2. The results indicate that sites II, V, VII, and XI, as well as the carboxy terminus, are the major continuous antigenic determinants on gD. In addition, the results show that the region from residues 264 through 369, except the transmembrane anchor, contains a series of continuous epitopes.
糖蛋白D(gD)是单纯疱疹病毒1型(HSV-1)和2型(HSV-2)病毒体包膜的一个组成部分,在病毒感染和发病机制中起重要作用。以前,抗gD单克隆抗体(MAb)被分为不同组,这些组识别HSV-1 gD(gD-1)和HSV-2 gD(gD-2)上不同的型共同和型特异性位点。几组识别依赖于三级结构的不连续表位。三组,即VII组、II组和V组,识别天然和变性gD中都存在的连续表位。以前,II组由单个单克隆抗体DL6组成,其表位位于氨基酸268和287之间。在本文报道的研究中,我们扩展了对gD抗原结构的分析,重点关注连续表位。DL6表位被更精确地定位到残基272至279。另外鉴定出包括BD78在内的四种单克隆抗体,每种抗体识别残基264至275内的一个表位。BD78和DL6在与gD结合时相互阻断。此外,构建了一种gD的突变形式,其中273位的脯氨酸被丝氨酸取代。这种变化消除了gD中一个预测的β转角。两种抗体都不与这种突变体反应,表明BD78和DL6表位重叠,并在残基264至279内构成一个抗原位点(位点II)。单克隆抗体BD66识别一个单独的抗原位点(位点XI)(残基284至301)。该位点仅在位点II下游六个氨基酸处,但如阻断研究所示是不同的。用针对天然gD-1或gD-2的多克隆抗血清筛选模拟gD这些和其他区域的合成肽。结果表明,位点II、V、VII和XI以及羧基末端是gD上主要的连续抗原决定簇。此外,结果表明,除跨膜锚定区外,从残基264到369的区域包含一系列连续表位。