Shih T Y, Khoury G
Biochemistry. 1976 Feb 10;15(3):487-93. doi: 10.1021/bi00648a005.
SV40 DNA fragments chemically attached to neutral cellulose powder with a water-soluble carbodiimide have been used to isolate late lytic viral specific RNA from virus infected cells. Exhaustive hybridization to SV40 DNA reveals that virtually all of the isolated RNA molecules contain SV40 specific sequences. Comparison with SV40 cRNA prepared with purified Escherichia coli RNA polymerase and a SV40 DNA I template suggests that the purity of the isolated SV40 specific RNA is very close to 100%. The background level for the nonspecific binding of RNA to a purified cellulose matrix is very low. Retention of nonspecific RNA by SV40 DNA-cellulose is only 1.5% of the viral specific RNA isolated under saturating conditions for the column. Sedimentation in neutral sucrose suggests that the major 16S viral specific RNA has been isolated largely intact.
用一种水溶性碳二亚胺将SV40 DNA片段化学连接到中性纤维素粉末上,已被用于从病毒感染的细胞中分离晚期裂解病毒特异性RNA。与SV40 DNA的详尽杂交表明,几乎所有分离的RNA分子都含有SV40特异性序列。与用纯化的大肠杆菌RNA聚合酶和SV40 DNA I模板制备的SV40 cRNA比较表明,分离的SV40特异性RNA的纯度非常接近100%。RNA与纯化的纤维素基质非特异性结合的背景水平非常低。在柱的饱和条件下,SV40 DNA - 纤维素对非特异性RNA 的保留率仅为分离的病毒特异性RNA的1.5%。在中性蔗糖中的沉降表明,主要的16S病毒特异性RNA在很大程度上已完整分离。