Ribosomal catalysis - The evolution of mechanistic concepts for peptide bond formation and peptidyl-tRNA hydrolysis
被引:18
作者:
Erlacher, Matthias D.
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机构:
Innsbruck Med Univ, Div Genom & RN, Innsbruck Bioctr, A-6020 Innsbruck, AustriaInnsbruck Med Univ, Div Genom & RN, Innsbruck Bioctr, A-6020 Innsbruck, Austria
Erlacher, Matthias D.
[1
]
Polacek, Norbert
论文数: 0引用数: 0
h-index: 0
机构:
Innsbruck Med Univ, Div Genom & RN, Innsbruck Bioctr, A-6020 Innsbruck, AustriaInnsbruck Med Univ, Div Genom & RN, Innsbruck Bioctr, A-6020 Innsbruck, Austria
Polacek, Norbert
[1
]
机构:
[1] Innsbruck Med Univ, Div Genom & RN, Innsbruck Bioctr, A-6020 Innsbruck, Austria
ribosomes;
rRNA;
peptide bond formation;
peptidyl-tRNA hydrolysis;
translation termination;
protein synthesis;
ribozyme;
D O I:
10.4161/rna.5.1.5922
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Over time the mechanistic concepts to describe the two principal chemical reactions that are catalyzed by the ribosome, peptide bond formation and peptidyl-tRNA hydrolysis, have undergone dramatic changes. While the initial models were based on a ribosomal protein-based mechanism, evidence for a direct functional contribution of ribosomal RNA for catalysis has accumulated over the past years. The presentation of high resolution crystallographic structures of the large ribosomal subunit at the beginning of the new millennium dramatically increased our molecular insight into the organization of the active center and finally placed the ribosome amongst the list of RNA enzymes. Combined with elaborate biochemical and biophysical approaches the translation field has made significant progress in understanding mechanistic details of ribosomal catalysis. While it seems that the mechanism of ribosome-catalyzed peptidyl-tRNA hydrolysis is just emerging, the knowledge on transpeptidation is already very advanced. It has been realized that intricate interactions between ribosomal RNA and the transfer RNA substrate are crucial for proton shuttling that is required for efficient amide bond formation.