Aleksandrov Alexey, Simonson Thomas
Laboratoire de Biochimie (CNRS UMR7654), Department of Biology, Ecole Polytechnique, 91128 Palaiseau, France.
Biochemistry. 2008 Dec 23;47(51):13594-603. doi: 10.1021/bi801726q.
Tetracycline (Tc) is a broad-spectrum antibiotic that kills bacteria by interrupting protein biosynthesis. It is thought that the bacteriostatic action of Tc is associated with its binding to the acceptor site (or A site) in the bacterial ribosome, interfering with the attachment of aminoacyl-tRNA. Recently, however, the crystal structure of a complex between Tc and trypsin-modified elongation factor Tu (tm-EF-Tu) was determined, raising the question of whether Tc binding to EF-Tu has a role in its inhibition of protein synthesis. We address this question using computer simulations. As controls, we first compute relative ribosome binding free energies for seven Tc variants for which experimental data are available, obtaining good agreement. We then consider the binding of Tc to both the trypsin-modified and unmodified EF-Tu-GDP complexes. We show that the direct contribution of EF-Tu to the binding free energy is negligible; rather, the binding can be solely attributed to interactions of Tc with a bridging Mg(2+) ion and the GDP phosphate groups. The effects of trypsin modification are modest. Further, our calculations show that EF-Tu does not exhibit any binding preference for Tc over the nonantibiotic, 4-dedimethyl-Tc, and EF-Tu does not bind the Tc analogue tigecycline, which is a potent antibiotic. In contrast, both the ribosome and the Tet Repressor protein (involved in Tc resistance) do show a binding preference for Tc over 4-dedimethyl-Tc, and the ribosome prefers to bind tigecycline over Tc. Overall, our results provide insights into the binding properties of tetracyclines and support the idea that EF-Tu is not their primary target.
四环素(Tc)是一种广谱抗生素,通过干扰蛋白质生物合成来杀死细菌。人们认为Tc的抑菌作用与其与细菌核糖体中的受体位点(或A位点)结合有关,从而干扰氨酰tRNA的附着。然而,最近确定了Tc与胰蛋白酶修饰的延伸因子Tu(tm-EF-Tu)之间复合物的晶体结构,这就提出了一个问题,即Tc与EF-Tu的结合在其抑制蛋白质合成中是否起作用。我们使用计算机模拟来解决这个问题。作为对照,我们首先计算了七种有实验数据的Tc变体的相对核糖体结合自由能,结果吻合良好。然后我们考虑了Tc与胰蛋白酶修饰和未修饰的EF-Tu-GDP复合物的结合。我们发现EF-Tu对结合自由能的直接贡献可以忽略不计;相反,这种结合完全可以归因于Tc与桥连的Mg(2+)离子和GDP磷酸基团的相互作用。胰蛋白酶修饰的影响不大。此外,我们的计算表明,EF-Tu对Tc的结合偏好并不高于非抗生素4-去二甲基-Tc,并且EF-Tu不结合Tc类似物替加环素,而替加环素是一种强效抗生素。相比之下,核糖体和四环素阻遏蛋白(参与Tc抗性)对Tc的结合偏好确实高于4-去二甲基-Tc,并且核糖体更倾向于结合替加环素而非Tc。总体而言,我们的结果为四环素的结合特性提供了见解,并支持EF-Tu不是它们主要靶点的观点。