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基于荧光微孔板的蛋白质 - DNA 相互作用分析。I:固定化蛋白质。

Fluorescent microplate-based analysis of protein-DNA interactions. I: Immobilized protein.

作者信息

Zhang Zhan-Ren, Palfrey David, Nagel David A, Lambert Peter A, Jessop Robert A, Santos Albert F, Hine Anna V

机构信息

Aston University, Birmingham, UK.

出版信息

Biotechniques. 2003 Nov;35(5):980-2, 984, 986. doi: 10.2144/03355st06.

Abstract

A simple protein-DNA interaction analysis has been developed using a high-affinity/high-specificity zinc finger protein. In essence, purified protein samples are immobilized directly onto the surface of microplate wells, and fluorescently labeled DNA is added in solution. After incubation and washing, bound DNA is detected in a standard microplate reader. The minimum sensitivity of the assay is approximately 0.2 nM DNA. Since the detection of bound DNA is noninvasive and the protein-DNA interaction is not disrupted during detection, iterative readings may be taken from the same well, after successive alterations in interaction conditions, if required. In this respect, the assay may therefore be considered real time and permits appropriate interaction conditions to be determined quantitatively. The assay format is ideally suited to investigate the interactions of purified unlabeled DNA binding proteins in a high-throughput format.

摘要

利用高亲和力/高特异性锌指蛋白开发了一种简单的蛋白质 - DNA 相互作用分析方法。实质上,将纯化的蛋白质样品直接固定在微孔板孔的表面,然后在溶液中加入荧光标记的 DNA。孵育和洗涤后,在标准微孔板读数仪中检测结合的 DNA。该分析方法的最低灵敏度约为 0.2 nM DNA。由于结合 DNA 的检测是非侵入性的,并且在检测过程中蛋白质 - DNA 相互作用不会被破坏,因此如果需要,在相互作用条件连续改变后,可以从同一孔中进行重复读数。在这方面,该分析方法可被视为实时分析,并且能够定量确定合适的相互作用条件。该分析形式非常适合以高通量形式研究纯化的未标记 DNA 结合蛋白的相互作用。

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