Gopinath Subash C B, Misono Tomoko S, Kawasaki Kazunori, Mizuno Takafumi, Imai Masaki, Odagiri Takato, Kumar Penmetcha K R
Institute for Biological Resources and Functions, National Institute of Advanced Industrial Science and Technology, Central 6, 1-1 Higashi, Tsukuba City, Ibaraki 305-8566, Japan.
Department of Virology III, National Institute of Infectious Diseases, 4-7-1 Gakuen, Musashimurayama, Tokyo 208-0011, Japan.
J Gen Virol. 2006 Mar;87(Pt 3):479-487. doi: 10.1099/vir.0.81508-0.
Aptamers selected against various kinds of targets have shown remarkable specificity and affinity, similar to those displayed by antibodies to their antigens. To employ aptamers as genotyping reagents for the identification of pathogens and their strains, in vitro selections were carried out to find aptamers that specifically bind and distinguish the closely related human influenza A virus subtype H3N2. The selected aptamer, P30-10-16, binds specifically to the haemagglutinin (HA) region of the target strain A/Panama/2007/1999(H3N2) and failed to recognize other human influenza viruses, including another strain with the same subtype, H3N2. The aptamer displayed over 15-fold-higher affinity to the HA compared with the monoclonal antibody, and efficiently inhibited HA-mediated membrane fusion. These studies delineate the application of aptamers in the genotyping of viruses.
针对各种靶标筛选出的适体已显示出显著的特异性和亲和力,类似于抗体与其抗原所表现出的特性。为了将适体用作鉴定病原体及其菌株的基因分型试剂,进行了体外筛选以寻找能特异性结合并区分密切相关的人类甲型H3N2流感病毒的适体。筛选出的适体P30-10-16特异性结合靶标菌株A/巴拿马/2007/1999(H3N2)的血凝素(HA)区域,无法识别其他人类流感病毒,包括同一亚型的另一菌株H3N2。与单克隆抗体相比,该适体对HA的亲和力高出15倍以上,并能有效抑制HA介导的膜融合。这些研究阐述了适体在病毒基因分型中的应用。