Localizing protein-protein interactions by bimolecular fluorescence complementation in planta

被引:40
作者
Citovsky, Vitaly [2 ]
Gafni, Yedidya [3 ]
Tzfira, Tzvi [1 ]
机构
[1] Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
[2] SUNY Stony Brook, Dept Biochem & Cell Biol, Stony Brook, NY 11794 USA
[3] Volcani Ctr, ARO, Inst Plant Sci, IL-50250 Bet Dagan, Israel
关键词
fluorescent proteins; pSAT; confocal; plants; transformation; imaging; protein interactions; vector system;
D O I
10.1016/j.ymeth.2008.06.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The application of novel assays for basic cell research is tightly linked to the development of easy-to-use and versatile tools and protocols for implementing such technologies for a wide range of applications and model species. The bimolecular fluorescence complementation (BiFC) assay is one such novel method for which tools and protocols for its application in plant cell research are still being developed. BiFC is a powerful tool which enables not only detection, but also visualization and subcellular localization of protein-protein interactions in living cells. Here we describe the application of BiFC in plant cells while focusing on the use of our versatile set of vectors which were specifically designed to facilitate the transformation, expression and imaging of protein-protein interactions in various plant species. We discuss the considerations of using our system in various plant model systems, the use of single versus multiple expression cassettes, the application of our vectors using various transformation methods and the use of internal fluorescent markers which can assist in signal localization and easy data acquisition in living cells. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:196 / 206
页数:11
相关论文
共 72 条
[1]   FD, a bZIP protein mediating signals from the floral pathway integrator FT at the shoot apex [J].
Abe, M ;
Kobayashi, Y ;
Yamamoto, S ;
Daimon, Y ;
Yamaguchi, A ;
Ikeda, Y ;
Ichinoki, H ;
Notaguchi, M ;
Goto, K ;
Araki, T .
SCIENCE, 2005, 309 (5737) :1052-1056
[2]   VirE2, a type IV secretion substrate, interacts with the VirD4 transfer protein at cell poles of Agrobacterium tumefaciens [J].
Atmakuri, K ;
Ding, ZY ;
Christie, PJ .
MOLECULAR MICROBIOLOGY, 2003, 49 (06) :1699-1713
[3]   The visible touch: in planta visualization of protein-protein interactions by fluorophore-based methods [J].
Bhat, Riyaz A. ;
Lahaye, Thomas ;
Panstruga, Ralph .
PLANT METHODS, 2006, 2 (1)
[4]   Detection of protein-protein interactions in plants using bimolecular fluorescence complementation [J].
Bracha-Drori, K ;
Shichrur, K ;
Katz, A ;
Oliva, M ;
Angelovici, R ;
Yalovsky, S ;
Ohad, N .
PLANT JOURNAL, 2004, 40 (03) :419-427
[5]   Chloroplastic protein NRIP1 mediates innate immune receptor recognition of a viral effector [J].
Caplan, Jeffrey L. ;
Mamillapalli, Padmavathi ;
Burch-Smith, Tessa M. ;
Czymmek, Kirk ;
Dinesh-Kumar, S. P. .
CELL, 2008, 132 (03) :449-462
[6]   pSITE vectors for stable integration or transient expression of autofluorescent protein fusions in plants:: Probing Nicotiana benthamiana-virus interactions [J].
Chakrabarty, Romit ;
Banerjee, Rituparna ;
Chung, Sang-Min ;
Farman, Mark ;
Citovsky, Vitaly ;
Hogenhout, Saskia A. ;
Tzfira, Tzvi ;
Goodin, Michael .
MOLECULAR PLANT-MICROBE INTERACTIONS, 2007, 20 (07) :740-750
[7]   Effects of calreticulin on viral cell-to-cell movement [J].
Chen, MH ;
Tian, GW ;
Gafni, Y ;
Citovsky, V .
PLANT PHYSIOLOGY, 2005, 138 (04) :1866-1876
[8]  
CHERUKURI S, 2008, MOL BIOL CELL
[9]   A versatile vector system for multiple gene expression in plants [J].
Chung, SM ;
Frankman, EL ;
Tzfira, T .
TRENDS IN PLANT SCIENCE, 2005, 10 (08) :357-361
[10]   Subcellular localization of interacting proteins by bimolecular fluorescence complementation in planta [J].
Citovsky, Vitaly ;
Lee, Lan-Ying ;
Vyas, Shachi ;
Glick, Efrat ;
Chen, Min-Hue ;
Vainstein, Alexander ;
Gafni, Yedidya ;
Gelvin, Stanton B. ;
Tzfira, Tzvi .
JOURNAL OF MOLECULAR BIOLOGY, 2006, 362 (05) :1120-1131