Directional transition from initiation to elongation in bacterial translation

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The transition of the 30S initiation complex (IC) to the translating 70S ribosome after 50S subunit joining provides an important checkpoint for mRNA selection during translation in bacteria. Here, we study the timing and control of reactions that occur during 70S IC formation by rapid kinetic techn...

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Detalles Bibliográficos
Autores: Goyal, Akanksha, Belardinelli, Riccardo, Maracci, Cristina, Milon, Pohl, Rodnina, Marina V.
Formato: artículo
Fecha de Publicación:2015
Institución:Universidad Peruana de Ciencias Aplicadas
Repositorio:UPC-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorioacademico.upc.edu.pe:10757/579679
Enlace del recurso:http://hdl.handle.net/10757/579679
Nivel de acceso:acceso abierto
Materia:Elongation
Bacterial translation
Directional transition
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dc.title.es_PE.fl_str_mv Directional transition from initiation to elongation in bacterial translation
title Directional transition from initiation to elongation in bacterial translation
spellingShingle Directional transition from initiation to elongation in bacterial translation
Goyal, Akanksha
Elongation
Bacterial translation
Directional transition
title_short Directional transition from initiation to elongation in bacterial translation
title_full Directional transition from initiation to elongation in bacterial translation
title_fullStr Directional transition from initiation to elongation in bacterial translation
title_full_unstemmed Directional transition from initiation to elongation in bacterial translation
title_sort Directional transition from initiation to elongation in bacterial translation
author Goyal, Akanksha
author_facet Goyal, Akanksha
Belardinelli, Riccardo
Maracci, Cristina
Milon, Pohl
Rodnina, Marina V.
author_role author
author2 Belardinelli, Riccardo
Maracci, Cristina
Milon, Pohl
Rodnina, Marina V.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Goyal, Akanksha
Belardinelli, Riccardo
Maracci, Cristina
Milon, Pohl
Rodnina, Marina V.
dc.subject.es_PE.fl_str_mv Elongation
Bacterial translation
Directional transition
topic Elongation
Bacterial translation
Directional transition
description The transition of the 30S initiation complex (IC) to the translating 70S ribosome after 50S subunit joining provides an important checkpoint for mRNA selection during translation in bacteria. Here, we study the timing and control of reactions that occur during 70S IC formation by rapid kinetic techniques, using a toolbox of fluorescence-labeled translation components. We present a kinetic model based on global fitting of time courses obtained with eight different reporters at increasing concentrations of 50S subunits. IF1 and IF3 together affect the kinetics of subunit joining, but do not alter the elemental rates of subsequent steps of 70S IC maturation. After 50S subunit joining, IF2-dependent reactions take place independent of the presence of IF1 or IF3. GTP hydrolysis triggers the efficient dissociation of fMet-tRNAfMet from IF2 and promotes the dissociation of IF2 and IF1 from the 70S IC, but does not affect IF3. The presence of non-hydrolyzable GTP analogs shifts the equilibrium towards a stable 70S–mRNA–IF1–IF2–fMet-tRNAfMet complex. Our kinetic analysis reveals the molecular choreography of the late stages in translation initiation.
publishDate 2015
dc.date.accessioned.es_PE.fl_str_mv 2015-10-14T18:01:25Z
dc.date.available.es_PE.fl_str_mv 2015-10-14T18:01:25Z
dc.date.issued.fl_str_mv 2015-10-14
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dc.identifier.issn.es_PE.fl_str_mv 0305-1048
dc.identifier.doi.es_PE.fl_str_mv 10.1093/nar/gkv869
dc.identifier.uri.es_PE.fl_str_mv http://hdl.handle.net/10757/579679
dc.identifier.eissn.es_PE.fl_str_mv 1362-4962
dc.identifier.journal.es_PE.fl_str_mv Nucleic Acids Research (Nucleic Acids Research)
identifier_str_mv 0305-1048
10.1093/nar/gkv869
1362-4962
Nucleic Acids Research (Nucleic Acids Research)
url http://hdl.handle.net/10757/579679
dc.language.iso.es_PE.fl_str_mv eng
language eng
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dc.publisher.es_PE.fl_str_mv Oxford University Press
dc.source.es_PE.fl_str_mv Universidad Peruana de Ciencias Aplicadas (UPC)
Repositorio Académico - UPC
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spelling Goyal, AkankshaBelardinelli, RiccardoMaracci, CristinaMilon, PohlRodnina, Marina V.2015-10-14T18:01:25Z2015-10-14T18:01:25Z2015-10-140305-104810.1093/nar/gkv869http://hdl.handle.net/10757/5796791362-4962Nucleic Acids Research (Nucleic Acids Research)The transition of the 30S initiation complex (IC) to the translating 70S ribosome after 50S subunit joining provides an important checkpoint for mRNA selection during translation in bacteria. Here, we study the timing and control of reactions that occur during 70S IC formation by rapid kinetic techniques, using a toolbox of fluorescence-labeled translation components. We present a kinetic model based on global fitting of time courses obtained with eight different reporters at increasing concentrations of 50S subunits. IF1 and IF3 together affect the kinetics of subunit joining, but do not alter the elemental rates of subsequent steps of 70S IC maturation. After 50S subunit joining, IF2-dependent reactions take place independent of the presence of IF1 or IF3. GTP hydrolysis triggers the efficient dissociation of fMet-tRNAfMet from IF2 and promotes the dissociation of IF2 and IF1 from the 70S IC, but does not affect IF3. The presence of non-hydrolyzable GTP analogs shifts the equilibrium towards a stable 70S–mRNA–IF1–IF2–fMet-tRNAfMet complex. Our kinetic analysis reveals the molecular choreography of the late stages in translation initiation.Boehringen Ingelheim Fonds and the G¨ottingen Graduate School for Neurosciences, Biophysics, and Molecular Biosciences (to A.G.); Max Planck Society and grants of the Deutsche Forschungsgemeinschaft (to M.V.R.); Peruvian Programa Nacional de Innovaci ´on para la Competitividad y Productividad [382-PNICP-PIBA-2014 (to P.M.)]. Funding for open access charge: Max Planck Society.Revisión por paresapplication/pdfengOxford University Presshttp://nar.oxfordjournals.org/content/early/2015/09/03/nar.gkv869.full.pdf+htmlinfo:eu-repo/semantics/openAccessUniversidad Peruana de Ciencias Aplicadas (UPC)Repositorio Académico - UPCreponame:UPC-Institucionalinstname:Universidad Peruana de Ciencias Aplicadasinstacron:UPCElongationBacterial translationDirectional transitionDirectional transition from initiation to elongation in bacterial translationinfo:eu-repo/semantics/article2018-06-22T21:41:06ZThe transition of the 30S initiation complex (IC) to the translating 70S ribosome after 50S subunit joining provides an important checkpoint for mRNA selection during translation in bacteria. Here, we study the timing and control of reactions that occur during 70S IC formation by rapid kinetic techniques, using a toolbox of fluorescence-labeled translation components. We present a kinetic model based on global fitting of time courses obtained with eight different reporters at increasing concentrations of 50S subunits. IF1 and IF3 together affect the kinetics of subunit joining, but do not alter the elemental rates of subsequent steps of 70S IC maturation. After 50S subunit joining, IF2-dependent reactions take place independent of the presence of IF1 or IF3. GTP hydrolysis triggers the efficient dissociation of fMet-tRNAfMet from IF2 and promotes the dissociation of IF2 and IF1 from the 70S IC, but does not affect IF3. The presence of non-hydrolyzable GTP analogs shifts the equilibrium towards a stable 70S–mRNA–IF1–IF2–fMet-tRNAfMet complex. Our kinetic analysis reveals the molecular choreography of the late stages in translation initiation.ORIGINALNucl. Acids Res.-2015-Goyal-nar-gkv869.pdfNucl. 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