Venugopal K, Howes K, Barron G S, Payne L N
Institute for Animal Health, Compton, Nr. Newbury, Berkshire, United Kingdom.
Avian Dis. 1997 Apr-Jun;41(2):283-8.
We describe the construction of a recombinant baculovirus containing the cloned DNA encoding the gp85 envelope glycoprotein of HPRS-103 (subgroup J) avian leukosis virus fused to the carboxy-terminus of the affinity tag glutathione-S-transferase. The fusion protein was efficiently secreted into the supernatant medium of the infected insect cell culture and could be purified in a single step using immobilized glutathione. An enzyme-linked immunosorbent assay using the recombinant protein was found to be specific and sensitive for detection of HPRS-103 virus-specific antibodies in the sera of infected birds.
我们描述了一种重组杆状病毒的构建,该病毒含有克隆的DNA,编码与亲和标签谷胱甘肽-S-转移酶的羧基末端融合的HPRS-103(J亚群)禽白血病病毒的gp85包膜糖蛋白。融合蛋白被有效分泌到感染昆虫细胞培养物的上清培养基中,并且可以使用固定化谷胱甘肽一步纯化。发现使用重组蛋白的酶联免疫吸附测定法对检测感染禽类血清中的HPRS-103病毒特异性抗体具有特异性和敏感性。