In vitro analysis of DNA-protein interactions by proximity ligation.

@article{citeulike:1182082, abstract = {Protein-binding DNA sequence elements encode a variety of regulated functions of genomes. Information about such elements is currently in a state of rapid growth, but improved methods are required to characterize the sequence specificity of DNA-binding proteins. We have established an in vitro method for specific and sensitive solution-phase analysis of interactions between proteins and nucleic acids in nuclear extracts, based on the proximity ligation assay. The reagent consumption is very low, and the excellent sensitivity of the assay enables analysis of as few as 1-10 cells. We show that our results are highly reproducible, quantitative, and in good agreement with both EMSA and predictions obtained by using a motif finding software. This assay can be a valuable tool to characterize in-depth the sequence specificity of DNA-binding proteins and to evaluate effects of polymorphisms in known transcription factor binding sites.}, address = {Rudbeck Laboratory, Department of Genetics and Pathology, Uppsala University, Dag Hammarskj\"{o}ldsv\"{a}g 20, SE-75185 Uppsala, Sweden.}, author = {Gustafsdottir, S. M. and Schlingemann, J. and Rada-Iglesias, A. and Schallmeiner, E. and Kamali-Moghaddam, M. and Wadelius, C. and Landegren, U. }, citeulike-article-id = {1182082}, doi = {10.1073/pnas.0611229104}, issn = {0027-8424}, journal = {Proc Natl Acad Sci U S A}, keywords = {dna, interaction, protein}, month = {February}, number = {9}, pages = {3067--3072}, posted-at = {2007-04-23 04:06:15}, priority = {2}, title = {In vitro analysis of DNA-protein interactions by proximity ligation.}, url = {http://dx.doi.org/10.1073/pnas.0611229104}, volume = {104}, year = {2007} }

TY - JOUR ID - citeulike:1182082 L3 - citeulike-article-id:1182082 TI - In vitro analysis of DNA-protein interactions by proximity ligation. JF - Proc Natl Acad Sci U S A VL - 104 IS - 9 SP - 3067 EP - 3072 AD - Rudbeck Laboratory, Department of Genetics and Pathology, Uppsala University, Dag Hammarskjöldsväg 20, SE-75185 Uppsala, Sweden. SN - 0027-8424 N2 - Protein-binding DNA sequence elements encode a variety of regulated functions of genomes. Information about such elements is currently in a state of rapid growth, but improved methods are required to characterize the sequence specificity of DNA-binding proteins. We have established an in vitro method for specific and sensitive solution-phase analysis of interactions between proteins and nucleic acids in nuclear extracts, based on the proximity ligation assay. The reagent consumption is very low, and the excellent sensitivity of the assay enables analysis of as few as 1-10 cells. We show that our results are highly reproducible, quantitative, and in good agreement with both EMSA and predictions obtained by using a motif finding software. This assay can be a valuable tool to characterize in-depth the sequence specificity of DNA-binding proteins and to evaluate effects of polymorphisms in known transcription factor binding sites. KW - dna KW - interaction KW - protein AU - Gustafsdottir, SM AU - Schlingemann, J AU - Rada-Iglesias, A AU - Schallmeiner, E AU - Kamali-Moghaddam, M AU - Wadelius, C AU - Landegren, U PY - 2007/02/27/ UR - http://dx.doi.org/10.1073/pnas.0611229104 ER -