Efficient Ribosomal Peptidyl Transfer Critically Relies on the Presence of the Ribose 2‘-OH at A2451 of 23S rRNA
- 14 March 2006
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 128 (13) , 4453-4459
- https://doi.org/10.1021/ja0588454
Abstract
The ribosomal peptidyl transferase center is a ribozyme catalyzing peptide bond synthesis in all organisms. We applied a novel modified nucleoside interference approach to identify functional groups at 9 universally conserved active site residues. Owing to their immediate proximity to the chemical center, the 23S rRNA nucleosides A2451, U2506 and U2585 were of particular interest. Our study ruled out U2506 and U2585 as contributors of vital chemical groups for transpeptidation. In contrast the ribose 2‘-OH of A2451 was identified as the prime ribosomal group with potential functional importance. This 2‘-OH renders almost full catalytic power to the ribosome even when embedded into an active site of six neighboring 2‘-deoxyribose nucleosides. These data highlight the unique functional role of the A2451 2‘-OH for peptide bond synthesis among all other functional groups at the ribosomal peptidyl transferase active site.Keywords
This publication has 26 references indexed in Scilit:
- Structural Insights into the Roles of Water and the 2′ Hydroxyl of the P Site tRNA in the Peptidyl Transferase ReactionMolecular Cell, 2005
- The Ribosomal Peptidyl Transferase Center: Structure, Function, Evolution, InhibitionCritical Reviews in Biochemistry and Molecular Biology, 2005
- Substrate-assisted catalysis of peptide bond formation by the ribosomeNature Structural & Molecular Biology, 2004
- The Active Site of the Ribosome Is Composed of Two Layers of Conserved Nucleotides with Distinct Roles in Peptide Bond Formation and Peptide ReleaseCell, 2004
- New Strategies for Exploring RNA's 2′-OH Expose the Importance of Solvent during Group II Intron CatalysisChemistry & Biology, 2004
- SPARKA Novel Method To Monitor Ribosomal Peptidyl Transferase ActivityBiochemistry, 2002
- The Structural Basis of Ribosome Activity in Peptide Bond SynthesisScience, 2000
- Nucleosides and Nucleotides. 143. Synthesis of 5-Amino-4-imidazolecarboxamide (AICA) Deoxyribosides from Deoxyinosines and Their Conversion into 3-Deazapurine Derivatives.CHEMICAL & PHARMACEUTICAL BULLETIN, 1996
- Nucleosides. 121. Improved and general synthesis of 2'-deoxy-C-nucleosides. Synthesis of 5-(2-deoxy-.beta.-D-erythro-pentofuranosyl)uracil, -1-methyluracil, -1,3-dimethyluracil, and -isocytosineThe Journal of Organic Chemistry, 1982
- Ribosome-catalysed reaction of puromycin with a formylmethionine-containing oligonucleotideJournal of Molecular Biology, 1967