Chládek S, Ringer D, Abraham E M
Nucleic Acids Res. 1976 May;3(5):1215-24. doi: 10.1093/nar/3.5.1215.
2'(3')-O-L-Phenylalanylderivatives of fluorescent 1,N6-ethenoadenosine and 3,N4-ethenocytidine were prepared by chemical synthesis. Both compounds are good acceptor substrates in ribosomal peptidyltransferase reactions. Since these compounds cannot form Watson-Crick base pairs, the results indicate that the terminal aminoacyladenosine unit of AA-tRNA is bound to ribosomal protein on the acceptor site of peptidyltransferase and not to rRNA.
通过化学合成制备了荧光1,N6-乙烯腺苷和3,N4-乙烯胞苷的2'(3')-O-L-苯丙氨酰衍生物。这两种化合物在核糖体肽基转移酶反应中都是良好的受体底物。由于这些化合物不能形成沃森-克里克碱基对,结果表明,氨酰-tRNA的末端氨酰腺苷单元在肽基转移酶的受体位点与核糖体蛋白结合,而不是与rRNA结合。