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Mutational characterization and mapping of the 70S ribosome active site.
d'Aquino, Anne E; Azim, Tasfia; Aleksashin, Nikolay A; Hockenberry, Adam J; Krüger, Antje; Jewett, Michael C.
Afiliação
  • d'Aquino AE; Interdisciplinary Biological Sciences Program, Northwestern University, Evanston, IL 60208, USA.
  • Azim T; Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL 60208, USA.
  • Aleksashin NA; Chemistry of Life Processes Institute, Northwestern University, Evanston, IL 60208, USA.
  • Hockenberry AJ; Center for Synthetic Biology, Northwestern University, Evanston, IL 60208, USA.
  • Krüger A; Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL 60208, USA.
  • Jewett MC; Chemistry of Life Processes Institute, Northwestern University, Evanston, IL 60208, USA.
Nucleic Acids Res ; 48(5): 2777-2789, 2020 03 18.
Article em En | MEDLINE | ID: mdl-32009164
The synthetic capability of the Escherichia coli ribosome has attracted efforts to repurpose it for novel functions, such as the synthesis of polymers containing non-natural building blocks. However, efforts to repurpose ribosomes are limited by the lack of complete peptidyl transferase center (PTC) active site mutational analyses to inform design. To address this limitation, we leverage an in vitro ribosome synthesis platform to build and test every possible single nucleotide mutation within the PTC-ring, A-loop and P-loop, 180 total point mutations. These mutant ribosomes were characterized by assessing bulk protein synthesis kinetics, readthrough, assembly, and structure mapping. Despite the highly-conserved nature of the PTC, we found that >85% of the PTC nucleotides possess mutational flexibility. Our work represents a comprehensive single-point mutant characterization and mapping of the 70S ribosome's active site. We anticipate that it will facilitate structure-function relationships within the ribosome and make possible new synthetic biology applications.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ribossomos / Domínio Catalítico / Escherichia coli / Mutação Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ribossomos / Domínio Catalítico / Escherichia coli / Mutação Idioma: En Ano de publicação: 2020 Tipo de documento: Article