Lehtinen M, Parkkonen P, Niemelä J, Paavonen J
Institute of Biomedical Sciences, University of Tampere, Finland.
Biochem Biophys Res Commun. 1990 Nov 15;172(3):1378-83. doi: 10.1016/0006-291x(90)91602-o.
We studied human papillomavirus (HPV) minor nucleocapsid protein (L2) by epitope scanning. Conserved antigenic epitopes identified by rabbit antiserum to bovine papillomavirus (BPV) were revealed in HPV-6b (amino acids, aa, 196-205); HPV-16 (aa:s 376-85) and HPV-18 (aa:s 221-230). L2 proteins. The first two epitopes were situated in hydrophilic regions of the proteins. Aligning the aa-sequences that corresponded to the epitopes with the total L2 sequences of BPV and HPV1a revealed consensus motifs between BPV, HPV1a and the reactive HPV type. In the non-reactive types amino acid alterations were noted. Mismatch between HPV1a sequences and the corresponding HPV-6b and HPV-16, HPV-6b and HPV-18, and HPV-16 and HPV-18 sequences suggests that the alterations may have evolved to facilitate immune surveillance of the genital HPV types.
我们通过表位扫描研究了人乳头瘤病毒(HPV)次要核衣壳蛋白(L2)。用兔抗牛乳头瘤病毒(BPV)抗血清鉴定出的保守抗原表位在HPV - 6b(氨基酸,aa,196 - 205)、HPV - 16(aa:376 - 385)和HPV - 18(aa:221 - 230)中被发现。L2蛋白。前两个表位位于蛋白的亲水区。将与表位对应的氨基酸序列与BPV和HPV1a的总L2序列进行比对,揭示了BPV、HPV1a和反应性HPV类型之间的共有基序。在非反应性类型中发现了氨基酸改变。HPV1a序列与相应的HPV - 6b和HPV - 16、HPV - 6b和HPV - 18以及HPV - 16和HPV - 18序列之间的错配表明,这些改变可能是为了便于对生殖器HPV类型进行免疫监测而进化产生的。