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RNA结构基序在RNA-脂筏相互作用中的作用。

The role of RNA structural motifs in RNA-lipid raft interaction.

作者信息

Mańka Rafał, Sapoń Karolina, Zaziąbło Joanna, Janas Teresa, Czogalla Aleksander, Janas Tadeusz

机构信息

Institute of Biology, University of Opole, Kominka 6, 45-032, Opole, Poland.

Department of Cytobiochemistry, Faculty of Biotechnology, University of Wroclaw, F. Joliot‑Curie 14a, 50‑383, Wrocław, Poland.

出版信息

Sci Rep. 2025 Feb 25;15(1):6777. doi: 10.1038/s41598-025-91093-x.

Abstract

Here, we sought to determine the role of specific RNA structural motifs in the interaction of RNA with model lipid vesicles containing liquid-ordered domains (RAFT liposomes). We show that the presence of several small apical loops within RNA structure favors RNA affinity for RAFT liposomes while the increased number of nucleotides within bulges inhibits this affinity. FRET flow cytometry measurements confirmed a modulation of the interaction of RNA with plasma membrane by the presence of specific RNA structural motifs. The analysis of viral RNA fragments revealed that a long double helix at the apical loop increases the affinity of viral RNA to lipid rafts. The analysis of exosomal Y RNAs secreted by nematode parasites showed that the presence of the EXO-motif GGAG is strongly correlated to the presence of small number of large apical loops within RNA structure. These results show that RNA structural motifs can modulate RNA affinity to liquid-ordered membrane lipid raft domains thus suggesting the importance of these motifs both for the mechanism of RNA loading into extracellular vesicles, and for the development of RNA-based lipid biosensors for monitoring of viral RNAs in biofluids and wastewater.

摘要

在此,我们试图确定特定RNA结构基序在RNA与含有液态有序结构域的模型脂质囊泡(筏状脂质体)相互作用中的作用。我们发现,RNA结构中几个小的顶端环的存在有利于RNA对筏状脂质体的亲和力,而凸起内核苷酸数量的增加则会抑制这种亲和力。荧光共振能量转移流式细胞术测量证实,特定RNA结构基序的存在会调节RNA与质膜的相互作用。对病毒RNA片段的分析表明,顶端环处的长双螺旋增加了病毒RNA对脂筏的亲和力。对线虫寄生虫分泌的外泌体Y RNA的分析表明,EXO基序GGAG的存在与RNA结构中少量大顶端环的存在密切相关。这些结果表明,RNA结构基序可以调节RNA对液态有序膜脂筏结构域的亲和力,从而表明这些基序对于RNA加载到细胞外囊泡的机制以及用于监测生物流体和废水中病毒RNA的基于RNA的脂质生物传感器的开发都很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b676/11861254/68c43b11cef6/41598_2025_91093_Fig1_HTML.jpg

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