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Updated: Jul 20, 2025

Imaging Protein-protein Interactions in vivo
Published on: October 10, 2010
Protocol for deriving proximity, affinity, and stoichiometry of protein interactions using image-based quantitative
Colin Feldmann1, Michael Schänzler2, Manu Ben-Johny3
1Institute of Cardiovascular Physiology and Pathophysiology, Faculty of Medicine, Biomedical Center, LMU-Munich, 82152 Planegg-Martinsried, Germany; Institute of Neurophysiology, Medizinische Hochschule Hannover, 30625 Hannover, Germany.
Abstract:
Two-hybrid Förster resonance energy transfer (FRET) provides proximity, affinity, and stoichiometry information in binding interactions. We present an image-based approach that surpasses traditional two-hybrid FRET assays in precision and robustness. We outline instrument setup and image acquisition and further describe steps for image preprocessing and two-hybrid FRET analysis using provided software to simplify the workflow. This protocol is compatible with confocal microscopes for high-precision and imaging plate readers for high-throughput applications. A plasmid-based reference system supports fast establishment of the protocol. For complete details on the use and execution of this protocol, please refer to Rivas et al.1.

