Mikheeva A V, Ghendon Y Z
Arch Virol. 1982;74(4):299-310. doi: 10.1007/BF01314163.
A fraction of polysomes synthesizing fowl plague virus (FPV) haemagglutinin (HA) was isolated from an infected chick embryo fibroblast (CEF) culture using a double immunoprecipitation assay. In an immunoprecipitate of HA-synthesizing polysomes (HA precipitate) the content of the HA polypeptide was increased with respect to the M1 + NS1 polypeptides as compared to a preparation of unprecipitated polysomes. In the HA precipitate, besides mRNA coding for HA synthesis, we have detected mRNAs corresponding to genes 1, 2 and 3 coding for high molecular weight P proteins. Studies of a cytoplasmic extract (CE) from FPV-infected CEF cultures in a sucrose density gradient revealed a fraction of polysomes with a sedimentation value of about 500S; the composition of virus-specific polypeptides and mRNA of the fraction was similar to that of the HA precipitate. It is thought that P proteins are synthesized on membrane-bound polysomes located closely to HA-synthesizing polysomes.
使用双重免疫沉淀测定法,从感染的鸡胚成纤维细胞(CEF)培养物中分离出一小部分合成禽痘病毒(FPV)血凝素(HA)的多核糖体。在合成HA的多核糖体免疫沉淀物(HA沉淀物)中,与未沉淀的多核糖体制剂相比,HA多肽的含量相对于M1 + NS1多肽有所增加。在HA沉淀物中,除了编码HA合成的mRNA外,我们还检测到了与编码高分子量P蛋白的基因1、2和3相对应的mRNA。对FPV感染的CEF培养物的细胞质提取物(CE)在蔗糖密度梯度中的研究表明,有一部分多核糖体的沉降值约为500S;该部分病毒特异性多肽和mRNA的组成与HA沉淀物相似。据认为,P蛋白是在与合成HA的多核糖体紧密相邻的膜结合多核糖体上合成的。