Wang J G, Cullen J, Lemon S M
Department of Medicine, School of Medicine, University of North Carolina, Chapel Hill 27599-7030.
J Gen Virol. 1992 Jan;73 ( Pt 1):183-8. doi: 10.1099/0022-1317-73-1-183.
Antisera to a peptide representing the extreme carboxy terminus of the hepatitis delta virus antigen (HDAg) open reading frame (residues 197 to 211) recognized only the large (p27 delta) and not the small (p24 delta) form of HDAg in immunoblots of infected liver extracts, thereby providing direct proof that p27 delta and p24 delta differ in their carboxyl-terminal sequence and that p27 delta results from mutation within the stop codon terminating translation of p24 delta. Reactions with other peptide antisera demonstrated that multiple smaller virus-specified proteins were carboxy-terminally truncated forms of HDAg, and immunoprecipitation studies suggested that different forms of HDAg were present as heterologous complexes within the liver extract.
针对代表丁型肝炎病毒抗原(HDAg)开放阅读框极端羧基末端(第197至211位氨基酸)的肽段制备的抗血清,在感染肝脏提取物的免疫印迹中仅识别HDAg的大(p27δ)形式,而不识别小(p24δ)形式,从而直接证明p27δ和p24δ的羧基末端序列不同,且p27δ是由终止p24δ翻译的终止密码子内的突变产生的。与其他肽抗血清的反应表明,多种较小的病毒特异性蛋白是HDAg的羧基末端截短形式,免疫沉淀研究表明,不同形式的HDAg以异源复合物的形式存在于肝脏提取物中。