Ripalti A, Dal Monte P, Boccuni M C, Campanini F, Lazzarotto T, Campisi B, Ruan Q, Landini M P
Department of Microbiology, School of Medicine, St. Orsola General Hospital, University of Bologna, Italy.
J Virol Methods. 1994 Jan;46(1):39-50. doi: 10.1016/0166-0934(94)90015-9.
We isolated and characterized from a lambda gt11 expression library clones expressing portions of human cytomegalovirus (HCMV)-p52. This nonstructural viral protein is encoded by UL44 and is known to be one of the best IgM reactive antigens. The reactivity of these clones was studied with human antibody and the gene fragment coding for the most immune-reactive portion of p52 (aa 202-434) was cloned in a prokaryotic expression vector, pROS, which overexpresses the antigen as a fusion protein to a truncated molecule of beta-galactosidase.
我们从一个λgt11表达文库中分离并鉴定了表达人巨细胞病毒(HCMV)-p52部分片段的克隆。这种非结构病毒蛋白由UL44编码,并且已知是最佳的IgM反应性抗原之一。用人类抗体研究了这些克隆的反应性,并将编码p52最具免疫反应性部分(氨基酸202 - 434)的基因片段克隆到原核表达载体pROS中,该载体将抗原作为与截短的β-半乳糖苷酶分子的融合蛋白进行过表达。