Easterwood T R, Major F, Malhotra A, Harvey S C
Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham 35294.
Nucleic Acids Res. 1994 Sep 11;22(18):3779-86. doi: 10.1093/nar/22.18.3779.
In protein synthesis, peptide bond formation requires that the tRNA carrying the amino acid (A site tRNA) contact the tRNA carrying the growing peptide chain (P site tRNA) at their 3' termini. Two models have been proposed for the orientations of two tRNAs as they would be bound to the mRNA in the ribosome. Viewing the tRNA as an upside down L, anticodon loop pointing down, acceptor stem pointing right, and calling this the front view, the R (Rich) model would have the back of the P site tRNA facing the front of the A site tRNA. In the S (Sundaralingam) model the front of the P site tRNA faces the back of the A site tRNA. Models of two tRNAs bound to mRNA as they would be positioned in the ribosomal A and P sites have been created using MC-SYM, a constraint satisfaction search program designed to build nucleic acid structures. The models incorporate information from fluorescence energy transfer experiments and chemical crosslinks. The models that best answer the constraints are of the S variety, with no R conformations produced consistent with the constraints.
在蛋白质合成过程中,肽键形成需要携带氨基酸的tRNA(A位点tRNA)在其3'末端与携带正在增长的肽链的tRNA(P位点tRNA)接触。关于这两种tRNA在核糖体中与mRNA结合时的方向,已提出两种模型。将tRNA视为倒置的L形,反密码子环朝下,受体茎朝右,并将此称为正视图,R(Rich)模型中P位点tRNA的背面朝向A位点tRNA的正面。在S(Sundaralingam)模型中,P位点tRNA的正面朝向A位点tRNA的背面。使用MC - SYM(一种旨在构建核酸结构的约束满足搜索程序)创建了两种tRNA与mRNA结合时位于核糖体A和P位点的模型。这些模型纳入了荧光能量转移实验和化学交联的信息。最符合约束条件的模型是S型,没有产生与约束条件一致的R构象。