Pongs O, Stöffler G, Bald R W
Nucleic Acids Res. 1976 Jul;3(7):1635-46. doi: 10.1093/nar/3.7.1635.
An affinity analog with a 5-bromoacetamido uridine 5'-phosphate moiety bonded to the 3' end of A-U-G has been prepared with the aid of polynucleotide phosphorylase. This 3'-modified, chemically reactive A-U-G analog was used to probe the ribosomal codon binding site. The yield of the reaction depended strongly on the ribosomal source and was sensitive to salt-washing ribosomes. The major crosslinking product was identified to be protein S1. Since the reaction of this 3'-modified A-U-G programmed ribosomes for Met-tRNA-Met-M binding, it is concluded that protein S1 is located at or near the 3'-side of the ribosomal codon binding site.
借助多核苷酸磷酸化酶制备了一种亲和类似物,其5-溴乙酰氨基尿苷5'-磷酸部分连接到A-U-G的3'末端。这种3'修饰的、具有化学反应性的A-U-G类似物用于探测核糖体密码子结合位点。反应产率强烈依赖于核糖体来源,并且对盐洗核糖体敏感。主要的交联产物被鉴定为蛋白质S1。由于这种3'修饰的A-U-G与核糖体反应可使甲硫氨酰-tRNA-甲硫氨酸结合,因此得出结论,蛋白质S1位于核糖体密码子结合位点的3'侧或其附近。