Schmeing T Martin, Huang Kevin S, Kitchen David E, Strobel Scott A, Steitz Thomas A
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520, USA.
Mol Cell. 2005 Nov 11;20(3):437-48. doi: 10.1016/j.molcel.2005.09.006.
Peptide bond formation is catalyzed at the peptidyl transferase center (PTC) of the large ribosomal subunit. Crystal structures of the large ribosomal subunit of Haloarcula marismortui (Hma) complexed with several analogs that represent either the substrates or the transition state intermediate of the peptidyl transferase reaction show that this reaction proceeds through a tetrahedral intermediate with S chirality. The oxyanion of the tetrahedral intermediate interacts with a water molecule that is positioned by nucleotides A2637 (E. coli numbering, 2602) and (methyl)U2619(2584). There are no Mg2+ ions or monovalent metal ions observed in the PTC that could directly promote catalysis. The A76 2' hydroxyl of the peptidyl-tRNA is hydrogen bonded to the alpha-amino group and could facilitate peptide bond formation by substrate positioning and by acting as a proton shuttle between the alpha-amino group and the A76 3' hydroxyl of the peptidyl-tRNA.
肽键形成是在大核糖体亚基的肽基转移酶中心(PTC)催化的。嗜盐嗜碱菌(Hma)大核糖体亚基与几种代表肽基转移酶反应底物或过渡态中间体的类似物复合的晶体结构表明,该反应通过具有S手性的四面体中间体进行。四面体中间体的氧负离子与由核苷酸A2637(大肠杆菌编号,2602)和(甲基)U2619(2584)定位的水分子相互作用。在PTC中未观察到可直接促进催化作用的Mg2+离子或单价金属离子。肽基-tRNA的A76 2'羟基与α-氨基形成氢键,并可通过底物定位以及作为α-氨基与肽基-tRNA的A76 3'羟基之间的质子穿梭体来促进肽键形成。