Localization of the ribosomal protection protein Tet(O) on the ribosome and the mechanism of tetracycline resistance

被引:59
作者
Spahn, CMT
Blaha, G
Agrawal, RK
Penczek, P
Grassucci, RA
Trieber, CA
Connell, SR
Taylor, DE
Nierhaus, KH
Frank, J
机构
[1] Hlth Res Inc, Howard Hughes Med Inst, Albany, NY 12201 USA
[2] Wadsworth Ctr, Albany, NY 12201 USA
[3] SUNY Albany, Dept Biomed Sci, Albany, NY 12222 USA
[4] Max Planck Inst Mol Genet, AG Ribosomen, D-14195 Berlin, Germany
[5] Univ Alberta, Dept Med Microbiol & Immunol, Edmonton, AB T6G 2H7, Canada
关键词
D O I
10.1016/S1097-2765(01)00238-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 Angstrom 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.
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页码:1037 / 1045
页数:9
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