State Key Laboratory of Molecular Virology and Genetic Engineering, Institute of Pathogen Biology, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing 100730, China.
J Virol Methods. 2011 Nov;177(2):160-7. doi: 10.1016/j.jviromet.2011.07.014. Epub 2011 Jul 30.
Influenza viruses are known for their ability to change their antigenic structure and create new viral strains. Hemagglutinin (HA), for which 16 subtypes have been identified, is a major antigenic determinant essential for the pathogenesis of influenza A viruses. To predict and monitor future epidemics, it is critical to produce various HA subtype antigens conveniently and rapidly. A simple, effective, and economic method to generate subunit HA1 of all 16 HA subtypes as recombinant proteins (rHA1) is reported. rHA1 proteins are expressed in insect cells as secretory proteins after integration into a baculovirus expression vector containing a 6×His tag element and the signal peptide of the GP67 protein, a membrane glycoprotein identified in Autographa californica nuclear polyhedrosis virus. The proteins can be purified to ≥90% purity using a single Ni(2+)-chelating affinity chromatography step, yielding a recovery rate of about 50%. The rHA1 proteins elicit high titer antibodies in mice and show high specificity in Western blots. This study paves the way for subtype specific detection methods and for future studies of the immune relationships among the subtypes of influenza A virus HA proteins.
流感病毒以其改变抗原结构和产生新病毒株的能力而闻名。血凝素(HA)是一种主要的抗原决定簇,已鉴定出 16 种亚型,对于流感 A 病毒的发病机制至关重要。为了预测和监测未来的流行情况,方便、快速地生产各种 HA 亚型抗原至关重要。本文报道了一种简单、有效、经济的方法,可将所有 16 种 HA 亚型的亚单位 HA1 作为重组蛋白(rHA1)产生。rHA1 蛋白在昆虫细胞中作为分泌蛋白表达,整合到含有 6×His 标签元件和 GP67 蛋白信号肽的杆状病毒表达载体中,GP67 蛋白是在 Autographa californica 核多角体病毒中鉴定出的一种膜糖蛋白。这些蛋白可以通过单一的 Ni(2+)-螯合亲和层析步骤纯化至≥90%纯度,回收率约为 50%。rHA1 蛋白在小鼠中引起高滴度的抗体,并在 Western blot 中显示出高度特异性。这项研究为亚型特异性检测方法以及未来研究流感 A 病毒 HA 蛋白亚型之间的免疫关系铺平了道路。