McGinnis Jennifer L, Liu Qi, Lavender Christopher A, Devaraj Aishwarya, McClory Sean P, Fredrick Kurt, Weeks Kevin M
Department of Chemistry, University of North Carolina, Chapel Hill, NC 27599-3290; and.
Department of Microbiology, Ohio State Biochemistry Program, and Center for RNA Biology, The Ohio State University, Columbus, OH 43210.
Proc Natl Acad Sci U S A. 2015 Feb 24;112(8):2425-30. doi: 10.1073/pnas.1411514112. Epub 2015 Feb 9.
It was shown decades ago that purified 30S ribosome subunits readily interconvert between "active" and "inactive" conformations in a switch that involves changes in the functionally important neck and decoding regions. However, the physiological significance of this conformational change had remained unknown. In exponentially growing Escherichia coli cells, RNA SHAPE probing revealed that 16S rRNA largely adopts the inactive conformation in stably assembled, mature 30S subunits and the active conformation in translating (70S) ribosomes. Inactive 30S subunits bind mRNA as efficiently as active subunits but initiate translation more slowly. Mutations that inhibited interconversion between states compromised translation in vivo. Binding by the small antibiotic paromomycin induced the inactive-to-active conversion, consistent with a low-energy barrier between the two states. Despite the small energetic barrier between states, but consistent with slow translation initiation and a functional role in vivo, interconversion involved large-scale changes in structure in the neck region that likely propagate across the 30S body via helix 44. These findings suggest the inactive state is a biologically relevant alternate conformation that regulates ribosome function as a conformational switch.
数十年前就已表明,纯化的30S核糖体亚基在一种涉及功能重要的颈部和解码区域发生变化的转换过程中,很容易在“活性”和“非活性”构象之间相互转换。然而,这种构象变化的生理意义一直不为人知。在指数生长的大肠杆菌细胞中,RNA SHAPE探测显示,16S rRNA在稳定组装的成熟30S亚基中大多采用非活性构象,而在正在进行翻译的(70S)核糖体中采用活性构象。非活性30S亚基与mRNA的结合效率与活性亚基一样高,但起始翻译的速度更慢。抑制状态间相互转换的突变在体内损害了翻译。小抗生素巴龙霉素的结合诱导了从非活性到活性的转换,这与两种状态之间的低能量屏障一致。尽管两种状态之间的能量屏障较小,但与缓慢的翻译起始以及在体内的功能作用一致,相互转换涉及颈部区域结构的大规模变化,这种变化可能通过螺旋44在30S主体中传播。这些发现表明,非活性状态是一种生物学上相关的替代构象,作为一种构象开关调节核糖体功能。