Department of Biochemistry and Molecular Biophysics, Columbia University, New York, New York 10032, USA.
Nat Commun. 2013;4:1477. doi: 10.1038/ncomms2470.
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.
四环素耐药蛋白 Tet(O) 可保护细菌核糖体免受抗生素四环素的结合,它是一种翻译延伸因子 GTPase,在序列和结构上与延伸因子 EF-G 有显著的相似性。在这里,我们根据 9.6-Å 分辨率的冷冻电镜重建,呈现了一个 Tet(O)-结合的 70S 核糖体的原子模型。这个原子模型使我们能够识别 Tet(O)-核糖体结合位点,该位点涉及 Tet(O) 结构域 4 中的三个特征环。通过将这三个环的三个氨基酸尖端替换为单个甘氨酸残基,导致 Tet(O) 介导的四环素耐药性丧失。基于这些发现,可以从分子细节解释 Tet(O) 介导的四环素耐药性的机制。