Spatio-temporal protein interaction analysis using bimolecular fluorescence complementation in C. elegans

Dynamic protein-protein interactions (PPIs) shape all aspects of cellular biology. Thus, significant efforts have been made to develop assays testing binary PPIs. The transparency of C. elegans makes it a great model organism for fluorescence-based PPI detection in vivo . However, to date, there is currently a lack of quantitative PPI assays that also provide information on the subcellular location of protein interactions in C. elegans. Here, we have made several modifications to the original bimolecular fluorescence complementation (BiFC) assay used in C. elegans to make it more quantitative and spatio-temporally controlled. First, transgenes are expressed at single copy, reducing the variability associated with multi-copy expression. Second, we have added bicistronic reference fluorescent proteins to each transgene, allowing for the normalization and quantification of the PPI. Finally, we have incorporated the auxin-inducible degradation system, allowing for small-molecule inducible control of the PPI signal. We demonstrate the utility of our modified BiFC assay by testing several model PPIs. Thus, we anticipate that our updated BiFC approach will expand the available tools for studying PPIs in C. elegans , but similar logic could be applied to other model organisms amenable to transgenesis and in vivo fluorescent imaging.