» Articles » PMID: 11389850

Localization of the Ribosomal Protection Protein Tet(O) on the Ribosome and the Mechanism of Tetracycline Resistance

Overview
Journal Mol Cell
Publisher Cell Press
Specialty Cell Biology
Date 2001 Jun 8
PMID 11389850
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Tet(O) belongs to a class of ribosomal protection proteins that mediate tetracycline resistance. It is a G protein that shows significant sequence similarity to elongation factor EF-G. Here we present a cryo-electron microscopic reconstruction, at 16 A resolution, of its complex with the E. coli 70S ribosome. Tet(O) was bound in the presence of a noncleavable GTP analog to programmed ribosomal complexes carrying fMet-tRNA in the P site. Tet(O) is directly visible as a mass close to the A-site region, similar in shape and binding position to EF-G. However, there are important differences. One of them is the different location of the tip of domain IV, which in the Tet(O) case, does not overlap with the ribosomal A site but is directly adjacent to the primary tetracycline binding site. Our findings give insights into the mechanism of tetracycline resistance.

Citing Articles

Functions and Regulation of Translation Elongation Factors.

Xu B, Liu L, Song G Front Mol Biosci. 2022; 8:816398.

PMID: 35127825 PMC: 8807479. DOI: 10.3389/fmolb.2021.816398.


Target protection as a key antibiotic resistance mechanism.

Wilson D, Hauryliuk V, Atkinson G, ONeill A Nat Rev Microbiol. 2020; 18(11):637-648.

PMID: 32587401 DOI: 10.1038/s41579-020-0386-z.


Joachim Frank's Binding with the Ribosome.

Li W, Agrawal R Structure. 2019; 27(3):411-419.

PMID: 30595455 PMC: 11062599. DOI: 10.1016/j.str.2018.11.006.


A genetically engineered that senses and degrades tetracycline antibiotic residue.

Mu Z, Zou Z, Yang Y, Wang W, Xu Y, Huang J Synth Syst Biotechnol. 2018; 3(3):196-203.

PMID: 30345405 PMC: 6190513. DOI: 10.1016/j.synbio.2018.05.001.


The conserved GTPase HflX is a ribosome splitting factor that binds to the E-site of the bacterial ribosome.

Coatham M, Brandon H, Fischer J, Schummer T, Wieden H Nucleic Acids Res. 2016; 44(4):1952-61.

PMID: 26733579 PMC: 4770234. DOI: 10.1093/nar/gkv1524.