Protocol for conditional mapping of proximal interactomes of dimeric protein complexes using a BioID-based complementation approach

Here, we provide a protocol for conditional mapping of proximal interactomes of dimeric protein complexes using a BioID-based complementation approach. We describe steps for fusing amino- and carboxyl-terminal fragments of the biotin ligase TurboID to proteins known to interact within cells. This interaction drives re-formation of an active ligase and biotinylation of nearby proteins. We then detail procedures for capturing biotinylated proteins on a streptavidin affinity matrix for identification by mass spectrometry and Python-based scripts for identifying high-confidence proximal interactors. For complete details on the use and execution of this protocol, please refer to Rajkumar et al. 1