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整合光控正交反应(PLOR)和应变促进的叠氮-炔环加成反应(SPAAC)点击化学用于RNA的高效位点特异性荧光标记

Integrating PLOR and SPAAC Click Chemistry for Efficient Site-Specific Fluorescent Labeling of RNA.

作者信息

Xue Yanyan, Si Xiao, Yin Daxu, Zhang Shengzhe, Dai Hua

机构信息

Institute of Translational Medicine, School of Medicine, Yangzhou University, Yangzhou 225001, China.

The Key Laboratory of the Jiangsu Higher Education Institutions for Nucleic Acid & Cell Fate Regulation (Yangzhou University), Yangzhou 225001, China.

出版信息

Int J Mol Sci. 2025 Mar 13;26(6):2601. doi: 10.3390/ijms26062601.

Abstract

Precisely fluorescently labeling specific nucleotide sites of RNA is critical for gaining insights into the structure and function of RNA through multiple fluorescence detection techniques. The position-selective labeling of RNA (PLOR) method provides a promising strategy to achieve this, wherein the fluorophore-modified NTPs can be co-transcriptionally introduced to specific sites of nascent RNA by using T7 RNA polymerase (T7 RNAP). However, due to steric hindrance limitations, the efficiency of T7 RNAP in recognizing and incorporating large fluorophore-modified NTPs into RNA is far from satisfactory. To overcome this challenge, in this work, we developed an efficient PLOR variant (ePLOR) for the site-specific fluorescent labeling of RNA by integrating PLOR with a post-transcriptional SPAAC (strain-promoted azido-alkyne cycloaddition) click chemistry reaction. The efficiency of the SPAAC reaction occurring on RNA is nearly 100%. Consequently, ePLOR enables the precise fluorescent labeling of designated sites across various structural regions of SAM-VI riboswitch and adenine riboswitch RNA, with labeling and synthesis efficiencies that are 2-2.5 times higher than those of PLOR. The strategy developed in this work can be used for the efficient synthesis of a broader spectrum of long-strand RNAs with site-specific fluorescent labeling and greatly facilitate the detection of the structure and function of these RNAs.

摘要

通过多种荧光检测技术精确地对RNA的特定核苷酸位点进行荧光标记,对于深入了解RNA的结构和功能至关重要。RNA的位置选择性标记(PLOR)方法为实现这一目标提供了一种很有前景的策略,其中通过使用T7 RNA聚合酶(T7 RNAP),可以在转录过程中将荧光团修饰的NTP共转录引入新生RNA的特定位点。然而,由于空间位阻的限制,T7 RNAP识别并将大的荧光团修饰的NTP掺入RNA的效率远不能令人满意。为了克服这一挑战,在这项工作中,我们通过将PLOR与转录后SPAAC(应变促进的叠氮-炔环加成)点击化学反应相结合,开发了一种用于RNA位点特异性荧光标记的高效PLOR变体(ePLOR)。在RNA上发生的SPAAC反应效率接近100%。因此,ePLOR能够对SAM-VI核糖开关和腺嘌呤核糖开关RNA的各个结构区域的指定位点进行精确的荧光标记,其标记和合成效率比PLOR高2至2.5倍。这项工作中开发的策略可用于高效合成具有位点特异性荧光标记的更广泛的长链RNA,并极大地促进对这些RNA的结构和功能的检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38c8/11942227/8a39a16275b9/ijms-26-02601-g001.jpg

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