Mwangi Mary N, Baird Nathan J
Saint Joseph's University, Philadelphia, PA, USA.
MethodsX. 2024 Aug 28;13:102925. doi: 10.1016/j.mex.2024.102925. eCollection 2024 Dec.
A long-standing challenge in the study of RNA structure-function dynamics using fluorescence-based methods has been the precise attachment of fluorophores to structured RNA molecules. Despite significant advancements in the field, existing techniques have limitations, especially for 3' end labeling of long, structured RNAs. In response to this challenge, we developed a chemo-enzymatic method that uses Klenow DNA polymerase to label RNAs. In this method:•Klenow DNA polymerase adds an amino-modified nucleotide to the 3' end of the RNA, guided by the DNA oligonucleotide template.•An NHS-ester dye is then conjugated to the amino-modified RNA, forming a covalent amide bond.•For highly structured RNAs, DNA oligonucleotides complementary to the RNA disrupt pre-existing intramolecular RNA structures. This methodological advancement enables site-specific incorporation of a single modified nucleotide at the 3' terminus of various RNA substrates, irrespective of their length or secondary structure. The user-friendly nature of the technique, with minimal modifications required for different RNA targets, makes it readily adaptable by a broad range of researchers. This approach has the potential to significantly improve the development of functionalized RNA for various applications.
使用基于荧光的方法研究RNA结构-功能动力学一直面临的一个长期挑战是将荧光团精确连接到结构化RNA分子上。尽管该领域取得了重大进展,但现有技术仍存在局限性,尤其是对于长链结构化RNA的3'端标记。为应对这一挑战,我们开发了一种化学酶法,该方法使用Klenow DNA聚合酶对RNA进行标记。在该方法中:
Klenow DNA聚合酶在DNA寡核苷酸模板的引导下,将一个氨基修饰的核苷酸添加到RNA的3'端。
然后将NHS酯染料与氨基修饰的RNA偶联,形成共价酰胺键。
对于高度结构化的RNA,与RNA互补的DNA寡核苷酸会破坏预先存在的分子内RNA结构。这一方法学上的进步使得能够在各种RNA底物的3'末端位点特异性地掺入单个修饰核苷酸,而不论其长度或二级结构如何。该技术用户友好,针对不同的RNA靶标所需的修饰极少,使得广大研究人员都能轻松采用。这种方法有可能显著促进用于各种应用的功能化RNA的开发。