Identification of an RNA-protein bridge spanning the ribosomal subunit interface

Science. 1999 Sep 24;285(5436):2133-6. doi: 10.1126/science.285.5436.2133.

Abstract

The 7.8 angstrom crystal structure of the 70S ribosome reveals a discrete double-helical bridge (B4) that projects from the 50S subunit, making contact with the 30S subunit. Preliminary modeling studies localized its contact site, near the bottom of the platform, to the binding site for ribosomal protein S15. Directed hydroxyl radical probing from iron(II) tethered to S15 specifically cleaved nucleotides in the 715 loop of domain II of 23S ribosomal RNA, one of the known sites in 23S ribosomal RNA that are footprinted by the 30S subunit. Reconstitution studies show that protection of the 715 loop, but none of the other 30S-dependent protections, is correlated with the presence of S15 in the 30S subunit. The 715 loop is specifically protected by binding free S15 to 50S subunits. Moreover, the previously determined structure of a homologous stem-loop from U2 small nuclear RNA fits closely to the electron density of the bridge.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Comment

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / metabolism
  • Binding Sites
  • Crystallography, X-Ray
  • Escherichia coli / chemistry
  • Hydroxyl Radical
  • Nucleic Acid Conformation
  • Protein Conformation
  • RNA, Bacterial / chemistry*
  • RNA, Bacterial / metabolism
  • RNA, Ribosomal, 23S / chemistry*
  • RNA, Ribosomal, 23S / metabolism
  • RNA, Small Nuclear / chemistry
  • RNA, Small Nuclear / metabolism
  • Ribosomal Proteins / chemistry
  • Ribosomal Proteins / metabolism*
  • Ribosomes / chemistry*
  • Ribosomes / metabolism
  • Ribosomes / ultrastructure
  • Thermus thermophilus / chemistry

Substances

  • Bacterial Proteins
  • RNA, Bacterial
  • RNA, Ribosomal, 23S
  • RNA, Small Nuclear
  • Ribosomal Proteins
  • ribosomal protein S15
  • Hydroxyl Radical