Dillner J, Kallin B, Klein G, Jörnvall H, Alexander H, Lerner R
EMBO J. 1985 Jul;4(7):1813-8. doi: 10.1002/j.1460-2075.1985.tb03855.x.
Five peptides were synthesized on the basis of amino acid sequences predicted from the transformation-associated BamHI WYH region of the genome of the Epstein-Barr virus (EBV). Antisera to two peptides deduced from a 1.6-kb open reading frame in the BamHI H fragment identified an 87 000-dalton nuclear polypeptide that was present in EBV-carrying cell lines that expressed the second EBV-determined nuclear antigen (EBNA-2). This polypeptide was not detected in cell lines that carried EBV variants with a deleted BamHI WYH region or in EBV-negative cell lines. Three peptides deduced from the 1.6-kb open reading frame reacted with human EBNA-positive sera, but not with EBNA-negative sera. Following affinity purification with the peptides, two of the corresponding human antibodies also reacted with the 87 000-dalton polypeptide.
根据从爱泼斯坦 - 巴尔病毒(EBV)基因组中与转化相关的BamHI WYH区域预测的氨基酸序列合成了五种肽。从BamHI H片段中的一个1.6 kb开放阅读框推导出来的针对两种肽的抗血清鉴定出一种87000道尔顿的核多肽,该多肽存在于表达第二种EBV决定的核抗原(EBNA - 2)的携带EBV的细胞系中。在携带缺失BamHI WYH区域的EBV变体的细胞系或EBV阴性细胞系中未检测到这种多肽。从1.6 kb开放阅读框推导出来的三种肽与人类EBNA阳性血清发生反应,但与EBNA阴性血清不发生反应。用这些肽进行亲和纯化后,两种相应的人类抗体也与87000道尔顿的多肽发生反应。