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用于检测DNA结合蛋白的分子信标。

Molecular beacons for detecting DNA binding proteins.

作者信息

Heyduk Tomasz, Heyduk Ewa

机构信息

Edward A. Doisy Department of Biochemistry and Molecular Biology, St. Louis University Medical School, 1402 S. Grand Blvd., St. Louis, MO 63104, USA.

出版信息

Nat Biotechnol. 2002 Feb;20(2):171-6. doi: 10.1038/nbt0202-171.

Abstract

We report here a simple, rapid, homogeneous fluorescence assay, the molecular beacon assay, for the detection and quantification of sequence-specific DNA-binding proteins. The central feature of the assay is the protein-dependent association of two DNA fragments each containing about half of a DNA sequence defining a protein-binding site. Protein-dependent association of DNA fragments can be detected by any proximity-based spectroscopic signal, such as fluorescence resonance energy transfer (FRET) between fluorochromes introduced into these DNA molecules. The assay is fully homogeneous and requires no manipulations aside from mixing of the sample and the test solution. It offers flexibility with respect to the mode of signal detection and the fluorescence probe, and is compatible with multicolor simultaneous detection of several proteins. The assay can be used in research and medical diagnosis and for high-throughput screening of drugs targeted to DNA-binding proteins.

摘要

我们在此报告一种简单、快速的均相荧光检测法——分子信标检测法,用于检测和定量序列特异性DNA结合蛋白。该检测法的核心特点是两个DNA片段的蛋白质依赖性缔合,每个片段包含约一半定义蛋白质结合位点的DNA序列。DNA片段的蛋白质依赖性缔合可通过任何基于邻近性的光谱信号检测,例如引入这些DNA分子中的荧光染料之间的荧光共振能量转移(FRET)。该检测法完全是均相的,除了混合样品和测试溶液外无需任何操作。它在信号检测模式和荧光探针方面具有灵活性,并且与几种蛋白质的多色同时检测兼容。该检测法可用于研究和医学诊断,以及针对DNA结合蛋白的药物高通量筛选。

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