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In this chapter we describe how to perform an electrophoretic mobility shift assay (EMSA), also known as the band shift or gel retardation assay, to determine the binding site-size of the DNA binding protein using a series of DNA polymers. The binding site-size information of the DNA binding protein is a prerequisite for formulating any model of the proteins’ function in DNA replication. EMSA is simple and quick, and if needed, the use of radioactive DNA make it highly sensitive and allow us to “see” the formation of distinct complexes of the DNA binding protein. The expectation of EMSA is that, once the length of the nucleotides is sufficient for the binding of protein, the protein-DNA complex remains intact and migrates as distinct band during gel electrophoresis. In addition, once the length of the nucleotides is sufficient for the binding of two or more proteins, the protein-DNA complexes migrate as distinct bands, usually referred to as a super shift: the higher the oligomeric protein-DNA complex, the lower the electrophoretic mobility. This technique can be used for both highly sequence-specific (e.g., transcription factor) (1,2) and non-specific proteins (e.g., single-stranded DNA binding protein) (3-7).

Determination of the Binding Site-Size of the Protein-DNA Complex by Use of the Electrophoretic Mobility Shift Assay