首页> 外文期刊>Journal of molecular recognition: JMR >Combining atomic force and fluorescence microscopy for analysis of quantum-dot labeled protein-DNA complexes.
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Combining atomic force and fluorescence microscopy for analysis of quantum-dot labeled protein-DNA complexes.

机译:结合原子力和荧光显微镜分析量子点标记的蛋白质-DNA复合物。

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摘要

Atomic force microscopy (AFM) and fluorescence microscopy are widely used for the study of protein-DNA interactions. While AFM excels in its ability to elucidate structural detail and spatial arrangement, it lacks the ability to distinguish between similarly sized objects in a complex system. This information is readily accessible to optical imaging techniques via site-specific fluorescent labels, which enable the direct detection and identification of multiple components simultaneously. Here, we show how the utilization of semiconductor quantum dots (QDs), serving as contrast agents for both AFM topography and fluorescence imaging, facilitates the combination of both imaging techniques, and with the addition of a flow based DNA extension method for sample deposition, results in a powerful tool for the study of protein-DNA complexes. We demonstrate the inherent advantages of this novel combination of techniques by imaging individual RNA polymerases (RNAP) on T7 genomic DNA.
机译:原子力显微镜(AFM)和荧光显微镜被广泛用于蛋白质-DNA相互作用的研究。尽管AFM在阐明结构细节和空间排列方面具有出色的能力,但它缺乏在复杂系统中区分大小相似的物体的能力。光学成像技术可以通过特定位置的荧光标记轻松访问此信息,这些标记可以同时直接检测和识别多个成分。在这里,我们展示了利用半导体量子点(QD)作为AFM形貌和荧光成像的对比剂,如何促进两种成像技术的结合,以及添加基于流的DNA扩展方法进行样品沉积,为研究蛋白质-DNA复合物提供了强大的工具。我们通过在T7基因组DNA上成像单个RNA聚合酶(RNAP),证明了这种新颖技术组合的固有优势。

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