Two-hybrid systems are extremely powerful methods for detecting protein:protein interactions in vivo. The basis of two-hybrid systems is the modular domains found in some transcription factors: a DNA-binding domain, which binds to a specific DNA sequence, and a transcriptional activation domain, which interacts with the basal transcriptional machinery. A transcriptional activation domain in association with a DNA-binding domain will promote the assembly of RNA polymerase II complexes at the TATA box and increase transcription. In the CheckMate Mammalian Two-Hybrid System the DNA-binding domain and the transcriptional activation domain, produced by separate plasmids, are closely associated when one protein (X) fused to a DNA-binding domain interacts with a second protein (Y) fused to a transcriptional activation domain. In this system, interaction between proteins X and Y results in transcription of a reporter gene.|
Mammalian System: Interactions can be studied in the cell line of choice. Proteins are more likely to be in their native conformation. Post-translational modifications, such as glycosylation, phosphorylation and acylation, are better maintained. Convenient Quantitation: The Dual-Luciferase(R) Reporter Assay System is used for detection.Internal Control: Renilla luciferase normalizes transfection efficiency. Fast Transient Assay: Results obtained two days after transfection, as compared to 3-4 days with the yeast system. Stable Transfectants: The pACT Vector contains the neomycin phosphotransferase gene, which allows for selection of stable transfectants.