Ribosomal catalysis - The evolution of mechanistic concepts for peptide bond formation and peptidyl-tRNA hydrolysis

被引:18
作者
Erlacher, Matthias D. [1 ]
Polacek, Norbert [1 ]
机构
[1] Innsbruck Med Univ, Div Genom & RN, Innsbruck Bioctr, A-6020 Innsbruck, Austria
基金
奥地利科学基金会;
关键词
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.
引用
收藏
页码:5 / 12
页数:8
相关论文
共 58 条
[11]   Peptide bond formation does not involve acid-base catalysis by ribosomal residues [J].
Bieling, P ;
Beringer, M ;
Adio, S ;
Rodnina, MV .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2006, 13 (05) :423-428
[12]   HYDROLYSIS OF FMET TRANSFER RNA BY PEPTIDYL TRANSFERASE [J].
CASKEY, CT ;
BEAUDET, AL ;
SCOLNICK, EM ;
ROSMAN, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1971, 68 (12) :3163-&
[13]   Pentose nucleotides in the cytoplasm of growing tissues [J].
Caspersson, T ;
Schultz, J .
NATURE, 1939, 143 :602-603
[14]  
CLAUDE C, 1943, SCIENCE, V97, P451
[15]  
CRICK F H, 1958, Symp Soc Exp Biol, V12, P138
[16]   ORIGIN OF GENETIC CODE [J].
CRICK, FHC .
JOURNAL OF MOLECULAR BIOLOGY, 1968, 38 (03) :367-&
[17]   Molecular aspects of the ribosomal peptidyl transferase [J].
Dorner, S ;
Polacek, N ;
Schulmeister, U ;
Panuschka, C ;
Barta, A .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2002, 30 :1131-1137
[18]   Mononucleotide derivatives as ribosomal P-site substrates reveal an important contribution of the 2′-OH to activity [J].
Dorner, S ;
Panuschka, C ;
Schmid, W ;
Barta, A .
NUCLEIC ACIDS RESEARCH, 2003, 31 (22) :6536-6542
[19]   Efficient ribosomal peptidyl transfer critically relies on the presence of the ribose 2′-OH at A2451 of 23S rRNA [J].
Erlacher, MD ;
Lang, K ;
Wotzel, B ;
Rieder, R ;
Micura, R ;
Polacek, N .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (13) :4453-4459
[20]   Chemical engineering of the peptidyl transferase center reveals an important role of the 2′-hydroxyl group of A2451 [J].
Erlacher, MD ;
Lang, K ;
Shankaran, N ;
Wotzel, B ;
Hüttenhofer, A ;
Micura, R ;
Mankin, AS ;
Polacek, N .
NUCLEIC ACIDS RESEARCH, 2005, 33 (05) :1618-1627