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用于改善细胞递送和mRNA敲低的小分子干扰RNA模拟物比率型pH(sMiRpH)探针

siRNA-Mimetic Ratiometric pH (sMiRpH) Probes for Improving Cell Delivery and mRNA Knockdown.

作者信息

Herling Madison R, Lopez Vazquez Lizeth, Dmochowski Ivan J

机构信息

Department of Chemistry, University of Pennsylvania, 231 S. 34th Street, Philadelphia, Pennsylvania 19104-6323, United States.

出版信息

ACS Chem Biol. 2025 Feb 21;20(2):309-320. doi: 10.1021/acschembio.4c00545. Epub 2025 Feb 5.

Abstract

Second-generation siRNA-mimetic ratiometric pH probes (sMiRpH-2) were developed by hybridizing a 3'-FAM-labeled 2'-OMe RNA strand with a 3'-Cy5-labeled 25mer RNA strand. These duplexes demonstrated the silencing of cytoplasmic mRNA targets in HeLa cells as measured by RT-qPCR and supported by western blot analysis. Fluorescence intensity and lifetime measurements revealed that a single guanosine (G) positioned adjacent to FAM achieves substantial static quenching at pH 5, with additional collisional quenching rendering the dye almost nonemissive. A FAM-G π-π stacking interaction was evidenced by a red-shifted absorbance spectrum for FAM. Decreased quenching at near-neutral pH enhances the FAM dynamic range in the physiologic pH window and improves the differentiation in cells between endocytic entrapment and cytoplasmic release. Flow cytometric analysis of intracellular pH and uptake using sMiRpH-2 was corroborated by live cell confocal microscopy and found to be predictive of knockdown efficacy. A sMiRpH-2 probe successfully predicted the relative efficacy of two transfection agents in more challenging SK-OV-3 cells, which highlights its use for the rapid assessment of nonviral siRNA delivery vectors.

摘要

通过将3'-FAM标记的2'-OMe RNA链与3'-Cy5标记的25聚体RNA链杂交,开发了第二代模拟siRNA的比率型pH探针(sMiRpH-2)。如通过RT-qPCR所测量并得到蛋白质免疫印迹分析支持的那样,这些双链体在HeLa细胞中表现出对细胞质mRNA靶标的沉默作用。荧光强度和寿命测量结果显示,与FAM相邻的单个鸟苷(G)在pH 5时实现了显著的静态猝灭,额外的碰撞猝灭使染料几乎不发光。FAM的吸收光谱发生红移,证明了FAM-G π-π堆积相互作用。在接近中性的pH下猝灭作用减弱,扩大了FAM在生理pH窗口中的动态范围,并改善了细胞内吞捕获和细胞质释放之间的区分。使用sMiRpH-2对细胞内pH和摄取进行的流式细胞术分析得到了活细胞共聚焦显微镜的证实,并且发现其可预测敲低效果。一种sMiRpH-2探针成功预测了两种转染试剂在更具挑战性的SK-OV-3细胞中的相对效果,这突出了其在快速评估非病毒siRNA递送载体方面的用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/11854375/f8980e284e66/cb4c00545_0007.jpg

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