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Ribosome Structure, Function, and Early Evolution

Ribosomes are among the largest and most dynamic molecular motors. The structure and dynamics of translation initiation and elongation are reviewed. Three ribosome motions have been identified for initiation and translocation. A swivel motion between the head/beak and the body of the 30S subunit was...

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Autores principales: Opron, Kristopher, Burton, Zachary F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337491/
https://www.ncbi.nlm.nih.gov/pubmed/30583477
http://dx.doi.org/10.3390/ijms20010040
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author Opron, Kristopher
Burton, Zachary F.
author_facet Opron, Kristopher
Burton, Zachary F.
author_sort Opron, Kristopher
collection PubMed
description Ribosomes are among the largest and most dynamic molecular motors. The structure and dynamics of translation initiation and elongation are reviewed. Three ribosome motions have been identified for initiation and translocation. A swivel motion between the head/beak and the body of the 30S subunit was observed. A tilting dynamic of the head/beak versus the body of the 30S subunit was detected using simulations. A reversible ratcheting motion was seen between the 30S and the 50S subunits that slide relative to one another. The 30S–50S intersubunit contacts regulate translocation. IF2, EF-Tu, and EF-G are homologous G-protein GTPases that cycle on and off the same site on the ribosome. The ribosome, aminoacyl-tRNA synthetase (aaRS) enzymes, transfer ribonucleic acid (tRNA), and messenger ribonucleic acid (mRNA) form the core of information processing in cells and are coevolved. Surprisingly, class I and class II aaRS enzymes, with distinct and incompatible folds, are homologs. Divergence of class I and class II aaRS enzymes and coevolution of the genetic code are described by analysis of ancient archaeal species.
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spelling pubmed-63374912019-01-22 Ribosome Structure, Function, and Early Evolution Opron, Kristopher Burton, Zachary F. Int J Mol Sci Review Ribosomes are among the largest and most dynamic molecular motors. The structure and dynamics of translation initiation and elongation are reviewed. Three ribosome motions have been identified for initiation and translocation. A swivel motion between the head/beak and the body of the 30S subunit was observed. A tilting dynamic of the head/beak versus the body of the 30S subunit was detected using simulations. A reversible ratcheting motion was seen between the 30S and the 50S subunits that slide relative to one another. The 30S–50S intersubunit contacts regulate translocation. IF2, EF-Tu, and EF-G are homologous G-protein GTPases that cycle on and off the same site on the ribosome. The ribosome, aminoacyl-tRNA synthetase (aaRS) enzymes, transfer ribonucleic acid (tRNA), and messenger ribonucleic acid (mRNA) form the core of information processing in cells and are coevolved. Surprisingly, class I and class II aaRS enzymes, with distinct and incompatible folds, are homologs. Divergence of class I and class II aaRS enzymes and coevolution of the genetic code are described by analysis of ancient archaeal species. MDPI 2018-12-21 /pmc/articles/PMC6337491/ /pubmed/30583477 http://dx.doi.org/10.3390/ijms20010040 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Opron, Kristopher
Burton, Zachary F.
Ribosome Structure, Function, and Early Evolution
title Ribosome Structure, Function, and Early Evolution
title_full Ribosome Structure, Function, and Early Evolution
title_fullStr Ribosome Structure, Function, and Early Evolution
title_full_unstemmed Ribosome Structure, Function, and Early Evolution
title_short Ribosome Structure, Function, and Early Evolution
title_sort ribosome structure, function, and early evolution
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337491/
https://www.ncbi.nlm.nih.gov/pubmed/30583477
http://dx.doi.org/10.3390/ijms20010040
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