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The Proto‐Ribosome: An Ancient Nano‐machine for Peptide Bond Formation
Author(s) -
Davidovich Chen,
Belousoff Matthew,
Wekselman Itai,
Shapira Tal,
Krupkin Miri,
Zimmerman Ella,
Bashan Anat,
Yonath Ada
Publication year - 2010
Publication title -
israel journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.908
H-Index - 54
eISSN - 1869-5868
pISSN - 0021-2148
DOI - 10.1002/ijch.201000012
Subject(s) - ribosome , ribozyme , chemistry , transfer rna , peptide bond , a site , peptidyl transferase , rna , translation (biology) , ribosomal rna , internal ribosome entry site , shine dalgarno sequence , peptide , biochemistry , stereochemistry , gene , binding site , messenger rna
The ribosome is a ribozyme whose active site, the peptidyl transferase center (PTC), is situated within a highly conserved universal symmetrical region that connects all ribosomal functional centers involved in amino acid polymerization. The linkage between this elaborate architecture and A‐site tRNA position revealed that the A‐ to P‐site passage of the tRNA 3′ terminus during protein synthesis is performed by a rotary motion, synchronized with the overall tRNA/mRNA sideways movement, and guided by the PTC. This rotary motion leads to suitable stereochemistry for peptide bond formation as well as for substrate‐mediated catalysis. Analysis of the substrate binding modes to ribosomes led to the hypothesis that the ancient ribosome produced single peptide bonds and non‐coded chains, potentially in a similar manner to the modern PTC. Later in evolution, a mechanism, enabling some type of decoding genetic control triggered the emergence of the small ribosomal subunit or part of it. This seems to be the result of the appearance of reaction products that could have evolved after polypeptides capable of enzymatic function were generated sporadically, while an ancient stable RNA fold was converted into an old version of a tRNA molecule. Since in the contemporary ribosome, the symmetry relates only to the backbone fold and nucleotide orientations but not nucleotide sequences, it emphasizes the superiority of functional requirement over sequence conservation, and indicates that the PTC may have evolved by gene fusion or gene duplication.