Brakier-Gingras L, Phoenix P
Can J Biochem Cell Biol. 1984 May;62(5):231-44. doi: 10.1139/o84-033.
This review surveys the different experimental approaches which describe the binding of tRNA to mRNA-programmed ribosomes and the control of tRNA selection. This selection is best described by the two-step model proposed by Hopfield and demonstrated by Thompson and his collaborators. The model involves a first control at the initial reversible binding of tRNA to the ribosome and a second control, the proofreading control, which promotes rejection of the incorrect tRNA from a high-energy intermediate during the transition from the initial to the final binding state. Streptomycin, neomycin, and ribosomal fidelity mutations appear to affect both control steps. Their effect can be related to the location of the mutated ribosomal proteins and to the conformational changes induced in the ribosome by the misreading agents. An alteration of the first control probably results from a distortion of the codon-anticodon interaction, while an alteration of the second control may be caused by a change in the association between ribosomal subunits.
本综述探讨了描述tRNA与mRNA编程核糖体结合及tRNA选择控制的不同实验方法。这种选择最好用霍普菲尔德提出并由汤普森及其合作者证明的两步模型来描述。该模型涉及第一步控制,即tRNA与核糖体的初始可逆结合,以及第二步控制,即校对控制,它在从初始结合状态到最终结合状态的转变过程中促进从高能中间体中排斥错误的tRNA。链霉素、新霉素和核糖体保真度突变似乎会影响这两个控制步骤。它们的作用可能与突变核糖体蛋白的位置以及误读剂在核糖体中诱导的构象变化有关。第一步控制的改变可能是由于密码子-反密码子相互作用的扭曲,而第二步控制的改变可能是由于核糖体亚基之间结合的变化引起的。