Odom O W, Hardesty B
Clayton Foundation Biochemical Institute, Department of Chemistry, University of Texas, Austin 78712.
Biochimie. 1987 Sep;69(9):925-38. doi: 10.1016/0300-9084(87)90226-4.
Fluorescence techniques were used to detect changes in the conformation of tRNA(Phe) that may occur during the peptidyl transferase reaction in which the tRNA appears to move between binding sites on ribosomes. Such a conformational change may be a fundamental part of the translocation mechanism by which tRNA and mRNA are moved through ribosomes. E. coli tRNA(Phe) was specifically labeled on acp3U47 and s4U8 or at the D positions 16 and 20. The labeled tRNAs were bound to ribosomes as deacylated tRNA(Phe) or AcPhe-tRNA. Changes in fluorescence quantum yield and anisotropy were measured upon binding to the ribosomes and during the peptidyl transferase reaction. In one set of experiments non-radiative energy transfer was measured between a coumarin probe at position 16 or 20 and a fluorescein attached to acp3U47 on the same tRNA(Phe) molecule. The results indicate that the apparent distance between the probes increases during deacylation of AcPhe-tRNA as a result of peptide bond formation. All of the results are consistent with but in themselves do not conclusively establish that tRNA undergoes a conformational change as well as movement during the peptidyl transferase reaction.
荧光技术被用于检测苯丙氨酸转运RNA(tRNA(Phe))在肽基转移酶反应过程中可能发生的构象变化,在该反应中tRNA似乎在核糖体上的结合位点之间移动。这种构象变化可能是tRNA和mRNA在核糖体中移动的转位机制的一个基本部分。大肠杆菌的tRNA(Phe)在acp3U47和s4U8或在第16和20位的D位点上被特异性标记。标记的tRNA以脱酰基tRNA(Phe)或乙酰苯丙氨酰 - tRNA的形式与核糖体结合。在与核糖体结合时以及在肽基转移酶反应过程中测量荧光量子产率和各向异性的变化。在一组实验中,测量了位于第16或20位的香豆素探针与连接在同一tRNA(Phe)分子上acp3U47的荧光素之间的非辐射能量转移。结果表明,由于肽键形成,乙酰苯丙氨酰 - tRNA脱酰化过程中探针之间的表观距离增加。所有结果都与之相符,但就其本身而言,并不能确凿地证明tRNA在肽基转移酶反应过程中经历了构象变化以及移动。