Mechanism of Tetracycline Resistance by Ribosomal Protection Protein Tet(O)

نویسندگان

  • Wen Li
  • Gemma C. Atkinson
  • Nehal S. Thakor
  • Ülar Allas
  • Chuao-chao Lu
  • Kwok-Yan Chan
  • Tanel Tenson
  • Klaus Schulten
  • Kevin S. Wilson
  • Vasili Hauryliuk
  • Joachim Frank
چکیده

Tetracycline resistance protein Tet(O), which protects the bacterial ribosome from binding the antibiotic tetracycline, is a translational GTPase with significant similarity in both sequence and structure to the elongation factor EF-G. Here, we present an atomic model of the Tet(O)-bound 70S ribosome based on our cryo-electron microscopic reconstruction at 9.6-Å resolution. This atomic model allowed us to identify the Tet(O)-ribosome binding sites, which involve three characteristic loops in domain 4 of Tet(O). Replacements of the three amino-acid tips of these loops by a single glycine residue result in loss of Tet(O)-mediated tetracycline resistance. On the basis of these findings, the mechanism of Tet(O)-mediated tetracycline resistance can be explained in molecular detail.

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عنوان ژورنال:

دوره 4  شماره 

صفحات  -

تاریخ انتشار 2013