Institute of Pharmacy and Molecular Biotechnology, Heidelberg University, Im Neuenheimer Feld 364, D-69120 Heidelberg, Germany.
Nucleic Acids Res. 2012 Jan;40(2):861-70. doi: 10.1093/nar/gkr733. Epub 2011 Sep 14.
Chemical probing is a common method for the structural characterization of RNA. Typically, RNA is radioactively end-labelled, subjected to probing conditions, and the cleavage fragment pattern is analysed by gel electrophoresis. In recent years, many chemical modifications, like fluorophores, were introduced into RNA, but methods are lacking that detect the influence of the modification on the RNA structure with single-nucleotide resolution. Here, we first demonstrate that a 5'-terminal (32)P label can be replaced by a dye label for in-line probing of riboswitch RNAs. Next, we show that small, highly structured FRET-labelled Diels-Alderase ribozymes can be directly probed, using the internal or terminal FRET dyes as reporters. The probing patterns indeed reveal whether or not the attachment of the dyes influences the structure. The existence of two dye labels in typical FRET constructs is found to be beneficial, as 'duplexing' allows observation of the complete RNA on a single gel. Structural information can be derived from the probing gels by deconvolution of the superimposed band patterns. Finally, we use fluorescent in-line probing to experimentally validate the structural consequences of photocaging, unambiguously demonstrating the intentional destruction of selected elements of secondary or tertiary structure.
化学探测是一种常用于 RNA 结构特征分析的方法。通常,将 RNA 放射性末端标记,然后进行探测条件处理,通过凝胶电泳分析切割片段模式。近年来,许多化学修饰物,如荧光染料,被引入 RNA 中,但缺乏能够以单核苷酸分辨率检测修饰对 RNA 结构影响的方法。在这里,我们首先证明可以用染料标记物代替 5'端(32)P 标记来进行核酶 RNA 的在线探测。接下来,我们表明,使用内部或末端 FRET 染料作为报告基团,可以直接探测到小的、高度结构的 FRET 标记的 Diels-Alderase 核酶。探测模式确实表明染料的附着是否会影响结构。在典型的 FRET 结构中存在两个染料标记物是有益的,因为“双链”允许在单个凝胶上观察完整的 RNA。可以通过对重叠带图案进行反卷积,从探测凝胶中得出结构信息。最后,我们使用荧光在线探测来实验验证光笼闭的结构后果,明确证明了对二级或三级结构的选定元件的有意破坏。