| Literature DB >> 14628672 |
Zhan-Ren Zhang1, David Palfrey, David A Nagel, Peter A Lambert, Robert A Jessop, Albert F Santos, Anna V Hine.
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.Mesh:
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Year: 2003 PMID: 14628672 DOI: 10.2144/03355st06
Source DB: PubMed Journal: Biotechniques ISSN: 0736-6205 Impact factor: 1.993