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在活细胞膜上对 RNA 特异性唾液酸化进行原位可视化,以探索糖基化位点。

In Situ Visualization of RNA-Specific Sialylation on Living Cell Membranes to Explore -Glycosylation Sites.

机构信息

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, P. R. China.

Shandong Province Key Laboratory of Detection Technology for Tumor Markers, School of Chemistry and Chemical Engineering, Linyi University, Linyi 276005, P. R. China.

出版信息

J Am Chem Soc. 2024 Mar 27;146(12):8780-8786. doi: 10.1021/jacs.4c01826. Epub 2024 Mar 18.

Abstract

The small RNAs on living cell membranes were recently found to be -glycosylated and terminated with sialic acids, although the glycosylation sites and potential functions remain unclear. Herein, we designed a second-generation hierarchical coding strategy (HieCo 2) for in situ visualization of cell surface RNA-specific sialylation. After covalently binding DNA codes to sialic acids and then binding a DNA code to a target RNA via sequence specificity, cascade decoding processes were performed with subsequent signal amplification that enabled sensitive in situ visualization of low-abundance Y5 RNA-specific sialic acids on living cell membranes. The proposed strategy unveils the number of glycosylation sites on a single RNA and reveals the binding preference of glycosylated RNAs to different sialic acid binding-immunoglobulin lectin-type receptors, demonstrating a new route for exploration of the glycosylated RNA-related biological and pathological processes.

摘要

最近发现,活细胞膜上的小 RNA 被 - 糖基化,并以唾液酸结尾,尽管糖基化位点和潜在功能仍不清楚。在此,我们设计了一种第二代层次编码策略(HieCo 2),用于原位可视化细胞表面 RNA 特异性唾液酸化。通过共价键将 DNA 编码与唾液酸结合,然后通过序列特异性将 DNA 编码与靶 RNA 结合,然后进行级联解码过程,随后进行信号放大,从而能够对活细胞膜上低丰度 Y5 RNA 特异性唾液酸进行敏感的原位可视化。所提出的策略揭示了单个 RNA 上的糖基化位点数量,并揭示了糖基化 RNA 与不同唾液酸结合免疫球蛋白样凝集素型受体的结合偏好性,为探索糖基化 RNA 相关的生物学和病理学过程开辟了新途径。

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