Kellings K, Meyer N, Mirenda C, Prusiner S B, Riesner D
Heinrich-Heine-Universität Düsseldorf, Federal Republic of Germany.
Arch Virol Suppl. 1993;7:215-25. doi: 10.1007/978-3-7091-9300-6_17.
Amount, type, and size of nucleic acid molecules associated with purified prion preparations were analyzed. Return refocusing gel electrophoresis (RRGE) was developed to detect homogeneous and heterogeneous nucleic acids extracted from highly purified scrapie prion preparations. With this method all types of nucleic acids in the size range from 13 to several thousand nucleotides could be analyzed. The recovery of all nucleic acids, after deproteinization and two-phase extraction was higher than 90%. Despite extensive nuclease digestions some small polynucleotides remained. Although a scrapie-specific nucleic acid cannot be excluded, the results further define the possible characteristics for such a hypothetical molecule. If it was homogeneous in size, then it would be < 80 nt in length at a particle-to-infectivity ratio (P/I) near unity; if the other extreme, i.e. totally heterogeneous scrapie-specific nucleic acids were assumed, then scrapie-specific nucleic acids would have to include molecules smaller than 240 nt. In order to exclude the possibility that unspecific background nucleic acid is entrapped in prion-rods, infectious material has to be prepared without a proteolysis and rod formation, and the analysis of nucleic acids performed with those preparations.
对与纯化朊病毒制剂相关的核酸分子的数量、类型和大小进行了分析。开发了回扫聚焦凝胶电泳(RRGE)来检测从高度纯化的羊瘙痒病朊病毒制剂中提取的均质和异质核酸。通过这种方法,可以分析大小范围从13到数千个核苷酸的所有类型的核酸。在脱蛋白和两相萃取后,所有核酸的回收率均高于90%。尽管进行了广泛的核酸酶消化,仍有一些小的多核苷酸残留。虽然不能排除存在羊瘙痒病特异性核酸,但这些结果进一步确定了这种假设分子可能具有的特征。如果其大小是均质的,那么在颗粒与感染性比率(P/I)接近1时,其长度将小于80个核苷酸;如果是另一种极端情况,即假设存在完全异质的羊瘙痒病特异性核酸,那么羊瘙痒病特异性核酸将必须包括小于240个核苷酸的分子。为了排除非特异性背景核酸被困在朊病毒杆中的可能性,必须在不进行蛋白水解和杆形成的情况下制备感染性物质,并用这些制剂进行核酸分析。