Comparing the BAD Protein Interactomes in 2D and 3D Cell Culture Using Proximity Labeling

• Published in: Journal of proteome research 2024-08, Vol.23 (8), p.3433-3443
• Main Authors: Pirayeshfard, Leila, Luo, Shu, Githaka, John Maringa, Saini, Arashdeep, Touret, Nicolas, Goping, Ing Swie, Julien, Olivier
• Format: Article
• Language: English
• Subjects: 14-3-3 Proteins - metabolism; bcl-Associated Death Protein - metabolism; bcl-X Protein - metabolism; Carbon-Nitrogen Ligases - genetics; Carbon-Nitrogen Ligases - metabolism; Cell Culture Techniques - methods; Escherichia coli Proteins - metabolism; Extracellular Matrix - metabolism; Humans; Protein Binding; Protein Interaction Mapping - methods; Protein Interaction Maps; Repressor Proteins
• ISSN: 1535-3893; 1535-3907; 1535-3907
• DOI: 10.1021/acs.jproteome.4c00111

Protein–protein interaction studies using proximity labeling techniques, such as biotin ligase-based BioID, have become integral in understanding cellular processes. Most studies utilize conventional 2D cell culture systems, potentially missing important differences in protein behavior found in 3D tissues. In this study, we investigated the protein–protein interactions of a protein, Bcl-2 Agonist of cell death (BAD), and compared conventional 2D culture conditions to a 3D system, wherein cells were embedded within a 3D extracellular matrix (ECM) mimic. Using BAD fused to the engineered biotin ligase miniTurbo (BirA*), we identified both overlapping and distinct BAD interactomes under 2D and 3D conditions. The known BAD binding proteins 14-3-3 isoforms and Bcl-XL interacted with BAD in both 2D and 3D. Of the 131 BAD-interactors identified, 56% were specific to 2D, 14% were specific to 3D, and 30% were common to both conditions. Interaction network analysis demonstrated differential associations between 2D and 3D interactomes, emphasizing the impact of the culture conditions on protein interactions. The 2D–3D overlap interactome encapsulated the apoptotic program, which is a well-known role of BAD. The 3D unique pathways were enriched in ECM signaling, suggestive of hitherto unknown functions for BAD. Thus, exploring protein–protein interactions in 3D provides novel clues into cell behavior. This exciting approach has the potential to bridge the knowledge gap between tractable 2D cell culture and organoid-like 3D systems.