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一种基于 DNA 四面体的非遗传邻近诱导 FRET 策略,用于可视化受体二聚化。

A Nongenetic Proximity-Induced FRET Strategy Based on DNA Tetrahedron for Visualizing the Receptor Dimerization.

机构信息

College of Chemistry, Chemical Engineering and Materials Science, Key Laboratory of Molecular and Nano Probes, Ministry of Education, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Institute of Molecular and Nano Science, Shandong Normal University, Jinan 250014, P. R. China.

出版信息

Anal Chem. 2020 Sep 1;92(17):11921-11926. doi: 10.1021/acs.analchem.0c02330. Epub 2020 Aug 5.

Abstract

Protein dimerization or oligomerization is a key factor in signal transduction processes. It is of great significance to develop novel strategies for investigating protein dimerization in cells and . Herein, we report a nongenetic proximity-induced fluorescence resonance energy transfer (FRET) strategy based on DNA tetrahedron for visualizing the receptor dimerization. In this nanostrategy, the aptamer serves as the recognition sequence for specifically binding to the receptor monomer. As long as the receptor dimers exist, the proximity switch probes hybridize with each other to induce the FRET between Cy3 and Cy5. Good stability of the DNA tetrahedron in this approach ensures the application value in multiple biological samples. This work provides a new way for developing novel protein dimerization visualization nanostrategies.

摘要

蛋白质二聚化或寡聚化是信号转导过程中的一个关键因素。因此,开发研究细胞内蛋白质二聚化的新策略具有重要意义。在此,我们报道了一种基于 DNA 四面体的非遗传邻近诱导荧光共振能量转移(FRET)策略,用于可视化受体二聚化。在这个纳米策略中,适体作为识别序列,特异性地与受体单体结合。只要受体二聚体存在,邻近开关探针就会相互杂交,从而在 Cy3 和 Cy5 之间产生 FRET。该方法中 DNA 四面体的良好稳定性确保了其在多种生物样品中的应用价值。这项工作为开发新的蛋白质二聚化可视化纳米策略提供了一种新方法。

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