Eaton B T, Regnery R L
J Gen Virol. 1975 Oct;29(1):35-49. doi: 10.1099/0022-1317-29-1-35.
Polysomes from Aedes albopictus cells were identified by their rapid labelling with radioactive amino acids and their sensitivity to EDTA, RNase and puromycin. The major ribosome component in cytoplasmic extracts had a sedimentation coefficient of approx. 95S and may be a ribosome dimer. In Semiki Forest virus infected Aedes albopictus cells, 42S and 26S RNA were the major virus RNA species detected up to 10 h post infection. Virus RNA was detected in association with pre-labelled ribosomes and banded at a buoyant density of 1-55 g/ml. 42S, 38S and 26S virus RNA species were associated with polysomes.
通过用放射性氨基酸快速标记以及对乙二胺四乙酸(EDTA)、核糖核酸酶(RNase)和嘌呤霉素的敏感性,鉴定出了白纹伊蚊细胞中的多核糖体。细胞质提取物中的主要核糖体成分沉降系数约为95S,可能是核糖体二聚体。在感染辛德毕斯病毒的白纹伊蚊细胞中,感染后10小时内检测到的主要病毒RNA种类是42S和26S RNA。病毒RNA与预先标记的核糖体相关联,其浮力密度为1.55克/毫升。42S、38S和26S病毒RNA种类与多核糖体相关。