Uwatoko K, Kano R, Sunairi M, Nakajima M, Yamaura K
Laboratory of Veterinary Virology, College of Agriculture and Veterinary Medicine, Nihon University, Kanagawa, Japan.
Vet Microbiol. 1996 Aug;51(3-4):267-73. doi: 10.1016/0378-1135(96)00049-1.
For identification of canine parvovirus (CPV) binding protein, the SDS-solubilized cell membrane fraction from a permissive cell line. CRPK, was subjected to the virus overlay protein blot assay (VOPBA). Competitive inhibition experiments showed the presence of multiple CPV-binding proteins with molecular masses of 36, 35, 33, 31, 29, 27, 25, and 23 kDa. CPV-binding proteins of same molecular masses were also detected in membrane fractions from nonpermissive, as well as other permissive, cell lines. We confirm that the mechanism of nonpermissiveness to CPV is not operative at the cellular attachment level.
为了鉴定犬细小病毒(CPV)结合蛋白,将来自敏感细胞系CRPK的十二烷基硫酸钠(SDS)增溶细胞膜组分进行病毒覆盖蛋白印迹分析(VOPBA)。竞争性抑制实验表明存在分子量为36、35、33、31、29、27、25和23 kDa的多种CPV结合蛋白。在非敏感细胞系以及其他敏感细胞系的膜组分中也检测到了相同分子量的CPV结合蛋白。我们证实,对CPV不敏感的机制在细胞附着水平不起作用。