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呼吸道合胞病毒A亚型和B亚型毒株之间的结构差异。

Structural differences between subtype A and B strains of respiratory syncytial virus.

作者信息

Norrby E, Mufson M A, Sheshberadaran H

出版信息

J Gen Virol. 1986 Dec;67 ( Pt 12):2721-9. doi: 10.1099/0022-1317-67-12-2721.

Abstract

Differences in the properties of homologous intracellular structural components of eight strains of subtype A and eight strains of subtype B of human respiratory syncytial (RS) virus were examined. The size of the fusion (F) protein cleavage products and the phosphoprotein (P) showed systematic differences between virus strains representing the two subtypes. The apparent mol. wt. in SDS-polyacrylamide gels under reducing conditions was 48,000 (48K) and 46K to 47K for the cleavage product F1 in subtype A and B strains, respectively. The size of the F2 protein was 18K to 20K. The subtype B strains showed a slightly higher mol. wt. of this protein compared to the subtype A strains. The size of the P protein was 36K in subtype A strains, but only 34K in subtype B strains. Variations also occurred in the size of the glycoprotein (G) and the 22K to 24K structural protein. These variations did not correlate with the virus subtypes, but were strain-specific. The size of non-glycosylated forms of the F protein cleavage products was determined by use of material from tunicamycin-treated cells. A 44K to 45K non-glycosylated form of the F1 protein was detected with subtype A virus strains, but the corresponding protein of subtype B strains was not reproducibly identified, presumably due to instability in the absence of glycosylation or altered antigenicity. Monoclonal antibody immunosorbent-bound viral glycoproteins were partially digested with proteases. The pattern of breakdown products of the F1 protein was distinctly different between subtype A and B strains, but it was similar among strains of the same subtype. No subtype-specific pattern was seen in proteolytic digests of monoclonal antibody-bound G protein.

摘要

对人类呼吸道合胞(RS)病毒A亚型的8个毒株和B亚型的8个毒株同源细胞内结构成分的特性差异进行了检测。代表这两个亚型的病毒毒株之间,融合(F)蛋白裂解产物和磷蛋白(P)的大小存在系统性差异。在还原条件下,SDS-聚丙烯酰胺凝胶中A亚型毒株F1裂解产物的表观分子量为48,000(48K),B亚型毒株为46K至47K。F2蛋白的大小为18K至20K。与A亚型毒株相比,B亚型毒株中该蛋白的分子量略高。A亚型毒株中P蛋白的大小为36K,而B亚型毒株中仅为34K。糖蛋白(G)和22K至24K结构蛋白的大小也存在差异。这些差异与病毒亚型无关,而是毒株特异性的。利用衣霉素处理细胞的材料测定了F蛋白裂解产物非糖基化形式的大小。在A亚型病毒毒株中检测到一种44K至45K的F1蛋白非糖基化形式,但B亚型毒株的相应蛋白未能重复鉴定出来,推测是由于在无糖基化情况下不稳定或抗原性改变。用蛋白酶对单克隆抗体免疫吸附结合的病毒糖蛋白进行部分消化。A亚型和B亚型毒株之间F1蛋白的降解产物模式明显不同,但同一亚型的毒株之间相似。在单克隆抗体结合的G蛋白的蛋白水解消化物中未观察到亚型特异性模式。

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