Your browser doesn't support javascript.
loading
Ribosome structure and dynamics by smFRET microscopy.
Shebl, Bassem; Norman, Zenia; Cornish, Peter V.
Afiliación
  • Shebl B; Department of Biochemistry, University of Missouri, Columbia, Missouri, USA.
  • Norman Z; Department of Biochemistry, University of Missouri, Columbia, Missouri, USA.
  • Cornish PV; Department of Biochemistry, University of Missouri, Columbia, Missouri, USA. Electronic address: cornishp@missouri.edu.
Methods Enzymol ; 549: 375-406, 2014.
Article en En | MEDLINE | ID: mdl-25432757
Composed of both RNA and protein components, the ribosome is one of the largest macromolecular machines in life responsible for the production of all protein. Interestingly, the major catalytic center of the ribosome (the peptidyl transferase center) and much of the binding regions for both mRNA and tRNA are composed of RNA making the ribosome one of the most complex and widely studied ribozymes. Further, large-scale conformational rearrangements throughout the ribosome are required for proper function making the ribosome a riboswitch as well. Recent advances in single-molecule biophysics have significantly augmented our understanding of ribosome function as both a ribozyme and riboswitch. Here, we discuss single-molecule Förster resonance energy transfer and its application to the study of the ribosome. Also, we describe how these experiments are designed from sample preparation to data acquisition and analysis. The general approach and methods described here can be generally applied to many other biological systems.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ribosomas / Transferencia Resonante de Energía de Fluorescencia Límite: Animals / Humans Idioma: En Revista: Methods Enzymol Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ribosomas / Transferencia Resonante de Energía de Fluorescencia Límite: Animals / Humans Idioma: En Revista: Methods Enzymol Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos