Protein Pull-Down

Affinity Pull-Down Assay

The pull-down assay is designed to determine the interaction of two or more proteins. With affinity pull-down assays, a ″bait″ protein is tagged and captured on an immobilized ligand (support beads) by covalent attachment or through an affinity tag such as immobilized metal affinity chromatography (IMAC). Common bait protein fusion tags include Glutathione S-transferase (GST) and histidine-tagged proteins. The bait protein forms a complex which is then incubated with a protein source such as cell or tissue lysate. The proteins of interest are eluted from the beaded support through a series of washes and collected by centrifugation. The affinity pull-down method of purification and detection is different from immunoprecipitation (IP) and Co-IP assays in that it is not an antibody to antigen interaction. With all pull-down assays, the purified sample is often analyzed by SDS-PAGE, mass spectral analysis, and western blot detection for further downstream analysis.

Affinity GST Pull-Down Applications

Glutathione S-transferase (GST) is a 211 amino acid protein that is found in most organisms. GST is often integrated into expression vectors to produce the fusion tag within E. coli protein expression systems. The GST-tag is a large protein tag, approximately 26 kDa, and can be expressed in bacteria, yeast, mammalian, and insect cells. The GST-tag is advantageous when protection of the recombinant protein from intracellular protease cleavage is required, and when there is a need to enhance the solubility of the tagged protein. In addition, the GST protein provides a high-affinity tag for easy purification and for pull-down experiments utilizing inexpensive affinity resins that are performed in mild elution conditions.


The pull-down assay is ideal for verification of co-immunoprecipitation results and an excellent method of identifying unknown protein-protein interactions along with the activation status of specific proteins. Unlike affinity pull-down methods, IP uses antibodies to bind to and isolate antigens from complex biological samples.

Co-IP refers to the use of an antibody to bind an antigen within a multiprotein complex. The complex is then captured with the addition of protein A or protein G medium. The high affinity of protein A/G to the Fc region of polyclonal and monoclonal IgG-type antibodies makes them a critical component in the purification of the protein or protein complex of interest. The use of protein pull-down methods is an essential tool for investigating protein-protein interaction networks; however, the choice of the specific method will be determined by the researcher’s specific application need.

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