Visualizing protein–protein interactions in plants by rapamycin-dependent delocalization. Issue 4 (25th January 2021)

• Record Type: Journal Article
• Authors: Winkler, Joanna; Mylle, Evelien; De Meyer, Andreas; Pavie, Benjamin; Merchie, Julie; Grones, Peter; Van Damme, Dani�l
• Is Part Of: The Plant Cell. Volume 33:Issue 4(2021)
• Page Start: 1101
• Page End: 1117
• Publication Date: 2021-01-25
• DOI: 10.1093/plcell/koab004
• Languages: English
• ISSNs: 1040-4651

Abstract

Abstract: Identifying protein–protein interactions (PPIs) is crucial for understanding biological processes. Many PPI tools are available, yet only some function within the context of a plant cell. Narrowing down even further, only a few tools allow complex multi-protein interactions to be visualized. Here, we present a conditional in vivo PPI tool for plant research that meets these criteria. Knocksideways in plants (KSP) is based on the ability of rapamycin to alter the localization of a bait protein and its interactors via the heterodimerization of FKBP and FRB domains. KSP is inherently free from many limitations of other PPI systems. This in vivo tool does not require spatial proximity of the bait and prey fluorophores and it is compatible with a broad range of fluorophores. KSP is also a conditional tool and therefore the visualization of the proteins in the absence of rapamycin acts as an internal control. We used KSP to confirm previously identified interactions in Nicotiana benthamiana leaf epidermal cells. Furthermore, the scripts that we generated allow the interactions to be quantified at high throughput. Finally, we demonstrate that KSP can easily be used to visualize complex multi-protein interactions. KSP is therefore a versatile tool with unique characteristics and applications that complements other plant PPI methods. Abstract : A tool based on rapamycin-dependent delocalization allows protein–protein interactions to be visualized and quantified inside Nicotiana benthamiana leaf epidermal cells.