Samson A C, Nesbit M, Lyon A M, Meulemans G
Department of Genetics, University of Newcastle upon Tyne, U.K.
J Gen Virol. 1988 Feb;69 ( Pt 2):473-80. doi: 10.1099/0022-1317-69-2-473.
A collection of monoclonal antibodies (MAbs) which react with the haemagglutinin-neuraminidase (HN) protein of Newcastle disease virus (NDV) has been used to isolate MAb-resistant mutants of the Beaudette C strain of NDV. The patterns of cross-reactivity of the HN proteins of these mutants against the collection of MAbs determined by Western blotting allowed the MAbs to be sorted into different groups. Protease V8 partial digest fragments of purified wild-type virions and subsequent reaction against the collection of MAbs using Western blotting provided an alternative method of grouping MAbs which broadly agreed with the former method. Chemical cleavage of the HN protein at aspartate-proline bonds followed by Western blotting of the fragments allowed the approximate position of certain MAb binding sites to be determined.
一组与新城疫病毒(NDV)血凝素神经氨酸酶(HN)蛋白发生反应的单克隆抗体(MAb)已被用于分离NDV博德特C株的单克隆抗体抗性突变体。通过蛋白质印迹法测定这些突变体的HN蛋白与该组单克隆抗体的交叉反应模式,可将单克隆抗体分为不同组。纯化的野生型病毒粒子的蛋白酶V8部分消化片段,以及随后通过蛋白质印迹法与该组单克隆抗体反应,提供了一种对单克隆抗体进行分组的替代方法,该方法与前一种方法大致相符。在天冬氨酸 - 脯氨酸键处对HN蛋白进行化学切割,然后对片段进行蛋白质印迹,可确定某些单克隆抗体结合位点的大致位置。