Thompson J, Kim D F, O'Connor M, Lieberman K R, Bayfield M A, Gregory S T, Green R, Noller H F, Dahlberg A E
Department of Molecular and Cell Biology and Biochemistry, Brown University, Providence, RI 02912, USA.
Proc Natl Acad Sci U S A. 2001 Jul 31;98(16):9002-7. doi: 10.1073/pnas.151257098. Epub 2001 Jul 24.
On the basis of the recent atomic-resolution x-ray structure of the 50S ribosomal subunit, residues A2451 and G2447 of 23S rRNA were proposed to participate directly in ribosome-catalyzed peptide bond formation. We have examined the peptidyltransferase and protein synthesis activities of ribosomes carrying mutations at these nucleotides. In Escherichia coli, pure mutant ribosome populations carrying either the G2447A or G2447C mutations maintained cell viability. In vitro, the G2447A ribosomes supported protein synthesis at a rate comparable to that of wild-type ribosomes. In single-turnover peptidyltransferase assays, G2447A ribosomes were shown to have essentially unimpaired peptidyltransferase activity at saturating substrate concentrations. All three base changes at the universally conserved A2451 conferred a dominant lethal phenotype when expressed in E. coli. Nonetheless, significant amounts of 2451 mutant ribosomes accumulated in polysomes, and all three 2451 mutations stimulated frameshifting and readthrough of stop codons in vivo. Furthermore, ribosomes carrying the A2451U transversion synthesized full-length beta-lactamase chains in vitro. Pure mutant ribosome populations with changes at A2451 were generated by reconstituting Bacillus stearothermophilus 50S subunits from in vitro transcribed 23S rRNA. In single-turnover peptidyltransferase assays, the rate of peptide bond formation was diminished 3- to 14-fold by these mutations. Peptidyltransferase activity and in vitro beta-lactamase synthesis by ribosomes with mutations at A2451 or G2447 were highly resistant to chloramphenicol. The significant levels of peptidyltransferase activity of ribosomes with mutations at A2451 and G2447 need to be reconciled with the roles proposed for these residues in catalysis.
基于最近解析的50S核糖体亚基的原子分辨率X射线结构,有人提出23S rRNA的A2451和G2447残基直接参与核糖体催化的肽键形成。我们研究了在这些核苷酸处携带突变的核糖体的肽基转移酶和蛋白质合成活性。在大肠杆菌中,携带G2447A或G2447C突变的纯突变核糖体群体能够维持细胞活力。在体外,G2447A核糖体支持蛋白质合成的速率与野生型核糖体相当。在单轮肽基转移酶测定中,G2447A核糖体在饱和底物浓度下显示出基本未受损的肽基转移酶活性。在大肠杆菌中表达时,普遍保守的A2451处的所有三个碱基变化都赋予了显性致死表型。尽管如此,大量的2451突变核糖体在多核糖体中积累,并且所有三个2451突变在体内刺激了移码和终止密码子的通读。此外,携带A2451U颠换的核糖体在体外合成了全长β-内酰胺酶链。通过从体外转录的23S rRNA重构嗜热栖热放线菌50S亚基,产生了在A2451处有变化的纯突变核糖体群体。在单轮肽基转移酶测定中,这些突变使肽键形成速率降低了3至14倍。A2451或G2447处有突变的核糖体的肽基转移酶活性和体外β-内酰胺酶合成对氯霉素具有高度抗性。A2451和G2447处有突变的核糖体的显著肽基转移酶活性水平需要与这些残基在催化中所提出的作用相协调。