Karathanasis S K, Champney W S
Biochemistry. 1979 May 15;18(10):2012-9. doi: 10.1021/bi00577a027.
16S rRNA reacted with the furocoumarin 4,5',8-trimethylpsoralen (trioxsalen) and 360-nm light showed a number of chemical and physical differences from untreated RNA. After extensive irradiation, five molecules of trioxsalen were bound per molecule of RNA. The trioxsalen-treated RNA had an altered ultraviolet absorption spectrum and a distinctive fluorescence emission spectrum. The modified RNA was significantly more resistant to T1 ribonuclease digestion than was control RNA. Treated RNA, when mixed with purified ribosomal proteins, was not functional in the in vitro reconstitution of 30S subunits and yielded more slowly sedimenting particles which were inactive in protein synthesis assays. By contrast, 16S rRNA within the 30S subunit structure did not exhibit these changes when reacted with the same dose of trioxsalen and light, suggesting that the ribosomal proteins were effective in protecting the RNA from interaction with the drug.
16S核糖体RNA与呋喃香豆素4,5',8-三甲基补骨脂素(三甲沙林)反应,并用360纳米光照射后,显示出与未处理的RNA在化学和物理方面的一些差异。经过大量照射后,每分子RNA结合了五个分子的三甲沙林。经三甲沙林处理的RNA具有改变的紫外吸收光谱和独特的荧光发射光谱。与对照RNA相比,经修饰的RNA对T1核糖核酸酶消化的抵抗力明显更强。经处理的RNA与纯化的核糖体蛋白混合时,在30S亚基的体外重组中无功能,并且产生沉降较慢的颗粒,这些颗粒在蛋白质合成测定中无活性。相比之下,30S亚基结构内的16S核糖体RNA在与相同剂量的三甲沙林和光反应时未表现出这些变化,这表明核糖体蛋白可有效保护RNA不与药物相互作用。