Protein-Protein Interactions: Co-Immunoprecipitation

Abstract

Proteins often do not function as single substances but rather as team players in a dynamic network. Growing evidence shows that protein-protein interactions are crucial in many biological processes in living cells. Genetic (such as yeast two-hybrid, Y2H) and biochemical (such as co-immunoprecipitation, co-IP) methods are the methods commonly used at the beginning of a study to identify the interacting proteins. Immunoprecipitation (IP), a method using a target protein-specific antibody in conjunction with Protein A/G affinity beads, is a powerful tool to identify molecules that interact with specific proteins. Therefore, co-IP is considered to be one of the standard methods of identifying or confirming the occurrence of protein-protein interaction events in vivo. Co-IP experiments can identify proteins via direct or indirect interactions or in a protein complex. Here, we use Agrobacterium type VI secretion system (T6SS) sheath components TssB-TssC₄₁ interaction as an example to describe the principle, procedure, and experimental problems of co-IP.

Keywords: Co-immunoprecipitation (Co-IP); Immobilization; Immunoprecipitation (IP); Physical interaction; Protein A/G Sepharose; Protein–protein interaction.