Screening for in planta protein-protein interactions combining bimolecular fluorescence complementation with flow cytometry
Screening for in planta protein-protein interactions combining bimolecular fluorescence complementation with flow cytometry
Abstract Understanding protein and gene function requires identifying interaction partners using biochemical, molecular or genetic tools. In plants, searching for novel protein-protein interactions is limited to protein purification assays, heterologous in vivo systems such as the yeast-two-hybrid or mutant screens. Ideally one would be able to search for novel protein partners in living plant cells. We demonstrate that it is possible to screen for novel protein-protein interactions from a random library in protoplasted Arabidopsis plant cells and recover some of the interacting partners. Our screen is based on capturing the bi-molecular complementation of mYFP between an YN-bait fusion partner and a completely random prey YC-cDNA library with FACS. The candidate interactions were confirmed using in planta BiFC assays and in planta FRET-FLIM assays. From this work, we show that the well characterized protein Calcium Dependent Protein Kinase 3 (CPK3) interacts with APX3, HMGB5, ORP2A and a ricin B-related lectin domain containing protein At2g39050. This is one of the first random in planta screens to be successfully employed.
- University of California System United States
- University of Tübingen Germany
- University of California, San Diego United States
- UNIVERSITY OF CALIFORNIA SAN DIEGO
- University of California, San Francisco United States
QH301-705.5, <it>In planta</it>, FACS, Methodology, Plant culture, Plant Science, CPK3, SB1-1110, <it>In vivo</it>, Genetics, Biology (General), BiFC, Protein-protein interaction screen, Biotechnology
QH301-705.5, <it>In planta</it>, FACS, Methodology, Plant culture, Plant Science, CPK3, SB1-1110, <it>In vivo</it>, Genetics, Biology (General), BiFC, Protein-protein interaction screen, Biotechnology
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