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DOI: 10.3791/53510-v
Graham S. Erwin1, Matthew P. Grieshop1, Devesh Bhimsaria1,2, Asuka Eguchi3, José A. Rodríguez-Martínez1, Aseem Z. Ansari1,4
1Department of Biochemistry,University of Wisconsin–Madison, 2Department of Electrical and Computer Engineering,University of Wisconsin–Madison, 3Graduate Program in Cellular and Molecular Biology,University of Wisconsin–Madison, 4The Genome Center,University of Wisconsin–Madison
This study presents a method for determining the genome-wide binding profiles of DNA-targeting small molecules, particularly polyamides. The technique, which involves crosslinking small molecules to isolate chromatin, provides insights into the direct interactions between ligands and DNA.
Identifying the direct targets of genome-targeting molecules remains a major challenge. To understand how DNA-binding molecules engage the genome, we developed a method that relies on crosslinking of small molecules to isolate chromatin (COSMIC).
The overall goal of this procedure is to determine the genome-wide binding profiles of polyamides and other DNA-targetting small molecules in cells. This method can help advance the field of drug DNA chemistry by using the genome to guide the design of DNA-targeting molecules. The main advantage of this technique is that direct ligand DNA interactions are measured to provide insight into the mechanism of action for ligands that act on the genome.
Some of most successful therapeutic agents are small molecules that bind to DNA and interfere with genomic transactions. Though this method was developed to study polyamides it can also be applied to other classes of DNA-targeting molecules. The cells for this experiment are grown in E8 Media on 10 cm dishes, with the surface coat that supports pluripotent stem cells at 37 degrees Celsius in a humidified atmosphere of 5%carbon dioxide.
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