Glutathione S-transferase fusion proteins as an affinity reagent for rapid isolation of specific sequence directly from genomic DNA
Author(s) -
Jerzy Majka,
Dagmara Jakimowicz,
Małgorzata Żarko-Postawka,
Jolanta ZakrzewskaCzerwińska
Publication year - 1997
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/25.12.2537
Subject(s) - biology , fusion protein , cosmid , microbiology and biotechnology , biochemistry , dna , genomic dna , glutathione s transferase , glutathione , affinity chromatography , transferase , enzyme , gene , recombinant dna
We describe a DNA binding assay for isolation of specific sequence(s) recognized by protein of interest directly from genomic or cosmid DNA. In our assay, the protein is fused to the glutathione-S-transferase and bound to glutathione-Sepharose beads. Then the immobilized fusion protein can be used to search for DNA fragment(s) that interact specifically with the protein of interest. As an example of such an approach, we identified and cloned a few prokaryotic oriC regions using the initiator DnaA protein fused to the glutathione-S-transferase.
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