Petersburg Nuclear Physics Institute, NRC "Kurchatov Institute", 188300 Gatchina, Russia.
Institute of Biomedical Systems and Biotechnology, Peter the Great St. Petersburg Polytechnic University, 195251 St. Petersburg, Russia.
Int J Mol Sci. 2021 Sep 5;22(17):9614. doi: 10.3390/ijms22179614.
The growth of the polypeptide chain occurs due to the fast and coordinated work of the ribosome and protein elongation factors, EF-Tu and EF-G. However, the exact contribution of each of these components in the overall balance of translation kinetics remains not fully understood. We created an in vitro translation system replacing either elongation factor with heterologous thermophilic protein from . The rates of the A-site binding and decoding reactions decreased an order of magnitude in the presence of thermophilic EF-Tu, indicating that the kinetics of aminoacyl-tRNA delivery depends on the properties of the elongation factor. On the contrary, thermophilic EF-G demonstrated the same translocation kinetics as a mesophilic protein. Effects of translocation inhibitors (spectinomycin, hygromycin B, viomycin and streptomycin) were also similar for both proteins. Thus, the process of translocation largely relies on the interaction of tRNAs and the ribosome and can be efficiently catalysed by thermophilic EF-G even at suboptimal temperatures.
多肽链的生长是由于核糖体和蛋白延伸因子 EF-Tu 和 EF-G 的快速协调工作。然而,这些成分在整体翻译动力学平衡中的具体贡献仍不完全清楚。我们创建了一个体外翻译系统,用来自 的异源嗜热蛋白替代延伸因子。在存在嗜热 EF-Tu 的情况下,A 位结合和解码反应的速率降低了一个数量级,这表明氨酰-tRNA 递呈的动力学取决于延伸因子的性质。相反,嗜热 EF-G 表现出与嗜温蛋白相同的转位动力学。转位抑制剂(壮观霉素、潮霉素 B、威霉素和链霉素)对两种蛋白的作用也相似。因此,转位过程在很大程度上依赖于 tRNA 和核糖体的相互作用,即使在亚最佳温度下,嗜热 EF-G 也能有效地催化转位。