Related Experiment Video
Updated: Apr 20, 2026

Bimolecular Fluorescence Complementation
Published on: April 15, 2011
BiFC for protein-protein interactions and protein topology: discussing an integrative approach for an old technique
Giovanni Stefano1, Luciana Renna, Federica Brandizzi
1MSU-DOE Plant Research Lab, Michigan State University, 612 Wilson Road, Room 206A, East Lansing, MI, 48824-1312, USA.
Abstract:
BiFC (Bimolecular Fluorescence Complementation) is one of the most widely used techniques to study protein-protein interactions as well as protein topology in living cells. This method allows the visualization of protein interactions or the analysis of their topology in the cell compartments where the proteins belong, without changing their chemical properties, as often occurs after mixing the content of different cellular compartments in cell extracts. Several laboratories use this method because it is relatively easy to perform; however, sometimes a positive protein-protein interaction BiFC signal (i.e., reconstitution of fluorescence of interacting protein pairs) does not necessarily mean that the tested proteins are actually interacting in vivo in a specific way. Here we describe the BiFC approach for assessing protein-protein interactions and for establishing protein topology and we discuss how to best perform this method to avoid false positive results when studying protein interactions in plant cells.
Related Concept Videos
Protein-protein Interfaces
Protein-Protein Interfaces
Protein Networks
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...
Protein Networks
Protein Organization
The primary structure of a protein is its amino acid sequence....
Protein Organization

