One-step affinity purification of the yeast ribosome and its associated proteins and mRNAs

Toshifumi Inada, Eric Winstall, Salvador Z. Tarun, John R. Yates, Dave Schieltz, Alan B. Sachs

Research output: Contribution to journalArticlepeer-review

96 Citations (Scopus)


We describe a one-step affinity method for purifying ribosomes from the budding yeast Saccharomyces cerevisiae. Extracts from yeast strains expressing only C-terminally tagged Rpl25 protein or overexpressing this protein in the presence of endogenous Rpl25p were used as the starting materials. The purification was specific for tagged 60S subunits, and resulted in the copurification of 80S subunits and polysomes, as well as ribosome-associated proteins and mRNAs. Two of these associated proteins, Mpt4p and Asc1p, were nearly stoichiometrically bound to the ribosome. In addition, the degree of mRNA association with the purified ribosomes was found to reflect the mRNA's translational status within the cell. The one-step purification of ribosome and its associated components from a crude extract should provide an important tool for future structural and biochemical studies of the ribosome, as well as for expression profiling of translated mRNAs.

Original languageEnglish
Pages (from-to)948-958
Number of pages11
Issue number7
Publication statusPublished - 2002
Externally publishedYes


  • 60S subunit
  • FLAG tag
  • Polysome
  • Ribosome-associated protein
  • Rpl25p
  • Translation

ASJC Scopus subject areas

  • Molecular Biology


Dive into the research topics of 'One-step affinity purification of the yeast ribosome and its associated proteins and mRNAs'. Together they form a unique fingerprint.

Cite this