Budker V G, Kobets N D, Kollektsionok I E, Karpova G G, Grineva N I
Mol Biol (Mosk). 1980 May-Jun;14(3):507-16.
4-(N-2-chloroethyl-N-methylamino)-benzaldehyde acetyl derivatives of penta-., hexa, hepta-, octauridylates were used for localization of the structures organizing the mRNA-binding centre of ribosomes. These derivatives, alike free oligonucleotides, stimulate the binding of phenylalanyl-tRNA to ribosomes. Within the specific complex all the oligonucleotide derivatives alkylated the 30S ribosomal subunit. Octauridylate and hexauridylate derivatives specifically alkylated also the 50S subunit of ribosomes. Polyuridylic acid protected ribosomal subunits from alkylation. In the 30S subunit the derivatives modify 16S RNA and proteins: S4, S5, S7, S9, S13, S15, S18, S21. It was found that oligouridylate derivatives of different length alkylate different proteins.
戊聚、己聚、庚聚、辛聚尿苷酸的4-(N-2-氯乙基-N-甲基氨基)-苯甲醛乙酰衍生物用于定位核糖体中组织mRNA结合中心的结构。这些衍生物与游离寡核苷酸一样,能刺激苯丙氨酰-tRNA与核糖体的结合。在特定复合物中,所有寡核苷酸衍生物都使30S核糖体亚基烷基化。辛聚尿苷酸和己聚尿苷酸衍生物还能特异性地使核糖体的50S亚基烷基化。聚尿苷酸可保护核糖体亚基不被烷基化。在30S亚基中,这些衍生物会修饰16S RNA和蛋白质:S4、S5、S7、S9、S13、S15、S18、S21。研究发现,不同长度的寡聚尿苷酸衍生物会使不同的蛋白质烷基化。