Promega's Cookie Policy

We use cookies and similar technologies to make our website work, run analytics, improve our website, and show you personalized content and advertising. Some of these cookies are essential for our website to work. For others, we won’t set them unless you accept them. To find out more about cookies and how to manage cookies, read our Cookie Policy.

Protein Interaction Analysis

Understanding which cellular molecules interact can help define protein pathways and recognition sites involved in gene expression. The HaloTag® Technology tool kit can capture both direct and indirect protein interactions as well as defining DNA binding sites and examining protein binding in live cells.

Characterize Binary and Higher Order Protein Complexes

Protein:protein interactions play critical roles in cellular processes, including replication, transcription, translation and signal transduction. The HaloTag® Mammalian Pull-Down Systems are designed to capture and purify intracellular binary and higher order protein complexes, including transient or weakly interacting partners. The covalent binding of the HaloTag® fusion bait protein means capturing the cellular protein complexes formed and identifying more physiologically relevant protein partners without interference from nonspecific binding.

Overview of the HaloTag® Mammalian Pull-Down System

HaloTag Pull-Down Overview for Protein:Protein Interactions

Capture Interacting Proteins for Investigation

p65 HaloTag fusion Protein Interactions

Expected cytoplasmic binary and tertiary protein interactions in the NFκB pathway were identified with specific p65-HaloTag® pull-down proteins identified by mass spectrometry were RelA(p65), RelB, C-Rel, IκBa, IκBb, IκBe, p100, p105(p50) and p52.

Study Protein:Protein Interactions in Live  Cells

Investigating dynamics of protein interactions can be challenging. Both induced and inhibited protein:protein interactions can be studied in real time under cellular conditions using the NanoBRET® PPI Assay. Based on bioluminescence resonance energy transfer (BRET) technique where a bioluminescent donor protein brought into close proximity to a fluorescently tagged acceptor protein, the NanoBRET® Assay harnesses the bright NanoLuc® luciferase as the energy donor and the HaloTag® protein labeled with a fluorophore as the energy acceptor. This sensitive PPI assay means you can study full-length proteins expressed at low levels.

Energy Transfer from NanoLuc to HaloTag NanoBRET Ligand 12749TA-W-a

Depiction of energy transfer from a NanoLuc®-Protein A fusion (energy donor) to a fluorescently labeled HaloTag®-Protein B fusion (energy acceptor) upon interaction of Protein A and Protein B.