Lenk M, Visser N, Mettenleiter T C
Institute of Molecular and Cellular Virology, Friedrich-Loeffler-Institutes, Federal Research Centre for Virus Diseases of Animals, Insel Riems, Germany.
J Virol. 1997 Jul;71(7):5635-8. doi: 10.1128/JVI.71.7.5635-5638.1997.
Positional homologs to the UL51 open reading frame of herpes simplex virus type 1 have been identified throughout the herpesvirus family. However, no respective protein has so far been described for any of the herpesviruses. With rabbit antisera directed against oligopeptides predicted to comprise antigenic regions of the deduced pseudorabies virus (PrV) UL51 protein, a polypeptide with a size of 30 kDa was identified in PrV-infected cell lysates and in purified virions. This molecular mass correlates reasonably well with the predicted mass of 25 kDa of the 236-amino-acid deduced UL51 protein. Antisera raised against peptides derived from different predicted antigenic regions all detected the 30-kDa protein in Western blot (immunoblot) analyses. Specificity was ascertained by peptide competition. Subcellular fractionation showed the presence of the UL51 protein mainly in the nucleus of infected cells. After separation of purified virion preparations into envelope and capsid, the PrV UL51 protein was detected in the capsid fraction. In summary, we identified the first herpesvirus UL51 protein and demonstrate that it represents a structural component of PrV virions.
在整个疱疹病毒家族中已鉴定出与单纯疱疹病毒1型UL51开放阅读框的位置同源物。然而,迄今为止,尚未对任何疱疹病毒描述相应的蛋白质。用针对预测包含推导的伪狂犬病病毒(PrV)UL51蛋白抗原区域的寡肽的兔抗血清,在PrV感染的细胞裂解物和纯化的病毒粒子中鉴定出一种大小为30 kDa的多肽。该分子量与推导的236个氨基酸的UL51蛋白预测的25 kDa分子量相当吻合。针对来自不同预测抗原区域的肽产生的抗血清在蛋白质印迹(免疫印迹)分析中均检测到30 kDa的蛋白质。通过肽竞争确定特异性。亚细胞分级分离显示UL51蛋白主要存在于受感染细胞的细胞核中。将纯化的病毒粒子制剂分离为包膜和衣壳后,在衣壳部分检测到PrV UL51蛋白。总之,我们鉴定出了首个疱疹病毒UL51蛋白,并证明它是PrV病毒粒子的一种结构成分。