Phase separation-based visualization of protein-protein interactions and kinase activities in plants

被引:8
|
作者
Safi, Alaeddine [1 ,2 ]
Smagghe, Wouter [1 ,2 ]
Goncalves, Amanda [3 ,4 ,5 ]
Wang, Qing [1 ,2 ]
Xu, Ke [1 ,2 ]
Fernandez, Ana Ibis [1 ,2 ]
Cappe, Benjamin [3 ,4 ,5 ]
Riquet, Franck B. [3 ,4 ,5 ,6 ]
Mylle, Evelien [1 ,2 ]
Eeckhout, Dominique [1 ,2 ]
De Winne, Nancy [1 ,2 ]
Van De Slijke, Eveline [1 ,2 ]
Persyn, Freya [1 ,2 ]
Persiau, Geert [1 ,2 ]
Van Damme, Daniel [1 ,2 ]
Geelen, Danny [7 ]
De Jaeger, Geert [1 ,2 ]
Beeckman, Tom [1 ,2 ]
Van Leene, Jelle [1 ,2 ]
Vanneste, Steffen [1 ,2 ,7 ]
机构
[1] Univ Ghent, Dept Plant Biotechnol & Bioinformat, B-9052 Ghent, Belgium
[2] Ctr Plant Syst Biol VIB, B-9052 Ghent, Belgium
[3] VIB Ugent Ctr Inflammat Res IRC, Cell Death & Inflammat Unit, Ghent, Belgium
[4] VIB, Bioimaging Core, B-9052 Ghent, Belgium
[5] Univ Ghent, Dept Biomed Mol Biol DBMB, Ghent, Belgium
[6] Univ Lille, CNRS, UMR 8523 PhLAM Phys Lasers Atomes & Mol, F-59000 Lille, France
[7] Univ Ghent, Dept Plants & Crops, B-9000 Ghent, Belgium
基金
欧洲研究理事会;
关键词
TANDEM AFFINITY PURIFICATION; COMPUTATIONAL DESIGN; TRANSCRIPTION FACTOR; FRET MICROSCOPY; ABSCISIC-ACID; ARABIDOPSIS; BINDING; DOMAIN; COMPLEXES; PHOSPHORYLATION;
D O I
10.1093/plcell/koad188
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein activities depend heavily on protein complex formation and dynamic posttranslational modifications, such as phosphorylation. The dynamic nature of protein complex formation and posttranslational modifications is notoriously difficult to monitor in planta at cellular resolution, often requiring extensive optimization. Here, we generated and exploited the SYnthetic Multivalency in PLants (SYMPL)-vector set to assay protein-protein interactions (PPIs) (separation of phases-based protein interaction reporter) and kinase activities (separation of phases-based activity reporter of kinase) in planta, based on phase separation. This technology enabled easy detection of inducible, binary and ternary PPIs among cytoplasmic and nuclear proteins in plant cells via a robust image-based readout. Moreover, we applied the SYMPL toolbox to develop an in vivo reporter for SNF1-related kinase 1 activity, allowing us to visualize tissue-specific, dynamic SnRK1 activity in stable transgenic Arabidopsis (Arabidopsis thaliana) plants. The SYMPL cloning toolbox provides a means to explore PPIs, phosphorylation, and other posttranslational modifications with unprecedented ease and sensitivity. Vectors for adding homo-oligomerizing tags were developed and used for detecting dynamic protein-protein interactions and phosphorylation changes in plants.
引用
收藏
页码:3280 / 3302
页数:23
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