Abstract
"Limited information exists for the binding specificities of many important transcription factors. To address this, we have previously developed a microwell- based assay for directly measuring the affinity of DNA- protein binding interactions. We describe here the detailed protocol for determining sequence specificities of DNA- binding proteins using this assay. The described method is rapid; after preparation of the reagents, the assay can be run in a single day, and its throughput can be increased further by automation. The method is quantitative but requires prior knowledge of one high- affinity binding site for the protein of interest. The protocol can be adapted for determining the effect of protein modifications and protein- protein interactions on DNA- binding specificity, and for engineering proteins with new DNA- binding specificities. In addition, the method is suitable for high- throughput screening to identify proteins or small molecules that modulate protein- DNA binding interactions."
Original language | English |
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Journal | Nature Protocols |
Volume | 1 |
Issue number | 1 |
Pages (from-to) | 215-222 |
Number of pages | 8 |
ISSN | 1754-2189 |
DOIs | |
Publication status | Published - 2006 |
MoE publication type | A1 Journal article-refereed |