Bhaduri S, Raskas H J, Green M
J Virol. 1972 Dec;10(6):1126-9. doi: 10.1128/JVI.10.6.1126-1129.1972.
Late after adenovirus 2 infection (18 hr), nearly all newly synthesized polysomal messenger ribonucleic acid (mRNA) is viral specified. Large amounts of adenovirus mRNA have been purified by utilizing membrane filtration at high ionic strength. With this procedure, molecules that contain polyadenylic acid [poly (A)] tracts are bound selectively, and ribosomal RNA can be separated from the viral mRNA which contains poly(A). Polysomal RNA synthesized 18 hr after infection was labeled in the presence of 0.02 mug of actinomycin D per ml and extracted at pH 9.0. This RNA annealed 40% to 3 mug of adenovirus 2 deoxyribonucleic acid; the RNA selected by membrane filtration bound 80% under the same conditions. The RNA eluted from membrane filters was 80 to 90% greater than 18S and contained species migrating as 31, 27, and 24S. Binding of polysomal RNA to individual membrane filters was linear, using as much as 300 mug of RNA per membrane. A 1.1-mg amount of viral RNA was prepared from 17.7 mg of polysomal RNA that had been purified by extraction at pH 9.0.
腺病毒2感染后期(18小时),几乎所有新合成的多核糖体信使核糖核酸(mRNA)都是病毒特异性的。利用高离子强度下的膜过滤已纯化出大量腺病毒mRNA。通过此程序,含有聚腺苷酸[聚(A)]序列的分子被选择性结合,核糖体RNA可与含有聚(A)的病毒mRNA分离。感染后18小时合成的多核糖体RNA在每毫升含0.02微克放线菌素D的情况下进行标记,并在pH 9.0条件下提取。这种RNA与3微克腺病毒2脱氧核糖核酸退火40%;在相同条件下,通过膜过滤选择的RNA结合率为80%。从膜过滤器洗脱的RNA比18S大80%至90%,并含有迁移为31S、27S和24S的物种。多核糖体RNA与单个膜过滤器的结合呈线性,每个膜使用多达300微克的RNA。从通过在pH 9.0条件下提取纯化的17.7毫克多核糖体RNA中制备了1.1毫克病毒RNA。