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Defining the sequence-recognition profile of DNA-binding molecules.


ABSTRACT: Determining the sequence-recognition properties of DNA-binding proteins and small molecules remains a major challenge. To address this need, we have developed a high-throughput approach that provides a comprehensive profile of the binding properties of DNA-binding molecules. The approach is based on displaying every permutation of a duplex DNA sequence (up to 10 positional variants) on a microfabricated array. The entire sequence space is interrogated simultaneously, and the affinity of a DNA-binding molecule for every sequence is obtained in a rapid, unbiased, and unsupervised manner. Using this platform, we have determined the full molecular recognition profile of an engineered small molecule and a eukaryotic transcription factor. The approach also yielded unique insights into the altered sequence-recognition landscapes as a result of cooperative assembly of DNA-binding molecules in a ternary complex. Solution studies strongly corroborated the sequence preferences identified by the array analysis.

SUBMITTER: Warren CL 

PROVIDER: S-EPMC1347994 | biostudies-literature | 2006 Jan

REPOSITORIES: biostudies-literature

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Defining the sequence-recognition profile of DNA-binding molecules.

Warren Christopher L CL   Kratochvil Natasha C S NC   Hauschild Karl E KE   Foister Shane S   Brezinski Mary L ML   Dervan Peter B PB   Phillips George N GN   Ansari Aseem Z AZ  

Proceedings of the National Academy of Sciences of the United States of America 20060117 4


Determining the sequence-recognition properties of DNA-binding proteins and small molecules remains a major challenge. To address this need, we have developed a high-throughput approach that provides a comprehensive profile of the binding properties of DNA-binding molecules. The approach is based on displaying every permutation of a duplex DNA sequence (up to 10 positional variants) on a microfabricated array. The entire sequence space is interrogated simultaneously, and the affinity of a DNA-bi  ...[more]

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