Welch A R, Woods A S, McNally L M, Cotter R J, Gibson W
Virology Laboratories, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10792-6. doi: 10.1073/pnas.88.23.10792.
A herpesvirus proteinase activity has been identified and partially characterized by using the cloned enzyme and substrate genes in transient transfection assays. Evidence is presented that the proteinase gene of cytomegalovirus strain Colburn encodes a 590-amino acid protein whose N-terminal 249 residues contain the proteolytic activity and two domains that are highly conserved in the homologous protein of other herpesviruses. Insertion of a short amino acid sequence between these domains abolished proteinase activity, suggesting that this region constitutes part or all of the enzyme active site. Plasma desorption mass spectrometry was used to identify the C terminus of the mature assembly protein as alanine, enabling the recognition of a consensus proteinase cleavage sequence of V/L-X-A decreases S/V, near the C-terminal end of all herpesvirus assembly protein homologs. Interestingly, the proteinase and its substrate, the assembly protein precursor, are encoded by opposite halves of the same open reading frame.
通过在瞬时转染试验中使用克隆的酶和底物基因,已鉴定出一种疱疹病毒蛋白酶活性并对其进行了部分表征。有证据表明,巨细胞病毒科尔本株的蛋白酶基因编码一种590个氨基酸的蛋白质,其N端的249个残基包含蛋白水解活性以及在其他疱疹病毒的同源蛋白中高度保守的两个结构域。在这些结构域之间插入一个短氨基酸序列会消除蛋白酶活性,这表明该区域构成了酶活性位点的一部分或全部。采用等离子体解吸质谱法确定成熟装配蛋白的C端为丙氨酸,从而识别出所有疱疹病毒装配蛋白同源物C端附近的一致蛋白酶切割序列V/L-X-A↓S/V。有趣的是,蛋白酶及其底物,即装配蛋白前体,由同一开放阅读框的相对两半编码。