Visualization of in vivo protein-protein interactions in plants

被引:9
作者
Strotmann, Vivien, I [1 ]
Stahl, Yvonne [1 ]
机构
[1] Heinrich Heine Univ, Inst Dev Genet, Univ Str 1, D-40225 Dusseldorf, Germany
关键词
BiFC; FRET; FRET-APB; FRET-FLIM; in planta; in vivo; protein-protein interaction (PPI); splitLuc; BIMOLECULAR FLUORESCENCE COMPLEMENTATION; RESONANCE ENERGY-TRANSFER; GENE-EXPRESSION; CO-IMMUNOPRECIPITATION; ARABIDOPSIS-THALIANA; COMPLEX-FORMATION; SPLIT LUCIFERASE; FRET; RECEPTOR; DYNAMICS;
D O I
10.1093/jxb/erac139
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Molecular processes depend on the concerted and dynamic interactions of proteins, either by one-on-one interactions of the same or different proteins or by the assembly of larger protein complexes consisting of many different proteins. Here, not only the protein-protein interaction (PPI) itself, but also the localization and activity of the protein of interest (POI) within the cell is essential. Therefore, in all cell biological experiments, preserving the spatio-temporal state of one POI relative to another is key to understanding the underlying complex and dynamic regulatory mechanisms in vivo. In this review, we examine some of the applicable techniques to measure PPIs in planta as well as recent combinatorial advances of PPI methods to measure the formation of higher order complexes with an emphasis on in vivo imaging techniques. We compare the different methods and discuss their benefits and potential pitfalls to facilitate the selection of appropriate techniques by providing a comprehensive overview of how to measure in vivo PPIs in plants. This review aims to provide a comprehensive and critical overview of techniques used to measure protein-protein interactions in living plants.
引用
收藏
页码:3866 / 3880
页数:15
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共 100 条
  • [61] PURIFICATION AND PROPERTIES OF RENILLA-RENIFORMIS LUCIFERASE
    MATTHEWS, JC
    HORI, K
    CORMIER, MJ
    [J]. BIOCHEMISTRY, 1977, 16 (01) : 85 - 91
  • [62] Dual luciferase assay system for rapid assessment of gene expression in Saccharomyces cerevisiae
    McNabb, DS
    Reed, R
    Marciniak, RA
    [J]. EUKARYOTIC CELL, 2005, 4 (09) : 1539 - 1549
  • [63] Timing and dynamics of single cell gene expression in the arabinose utilization system
    Megerle, Judith A.
    Fritz, Georg
    Gerland, Ulrich
    Jung, Kirsten
    Raedler, Joachim O.
    [J]. BIOPHYSICAL JOURNAL, 2008, 95 (04) : 2103 - 2115
  • [64] Mehlhorn DG, 2018, METHODS MOL BIOL, V1691, P139, DOI 10.1007/978-1-4939-7389-7_11
  • [65] Interaction proteomics
    Monti, M
    Orrù, S
    Pagnozzi, D
    Pucci, P
    [J]. BIOSCIENCE REPORTS, 2005, 25 (1-2) : 45 - 56
  • [66] Detection of transient protein-protein interactions by bimolecular fluorescence complementation:: The Abl-SH3 case
    Morell, Montse
    Espargaro, Alba
    Aviles, Francesc X.
    Ventura, Salvador
    [J]. PROTEOMICS, 2007, 7 (07) : 1023 - 1036
  • [67] Olejnik K, 2011, ACTA BIOCHIM POL, V58, P609
  • [68] Split luciferase as an optical probe for detecting protein-protein interactions in mammalian cells based on protein splicing
    Ozawa, T
    Kaihara, A
    Sato, M
    Tachihara, K
    Umezawa, Y
    [J]. ANALYTICAL CHEMISTRY, 2001, 73 (11) : 2516 - 2521
  • [69] Monitoring protein-protein interactions using split synthetic renilla luciferase protein-fragment-assisted complementation
    Paulmurugan, R
    Gambhir, SS
    [J]. ANALYTICAL CHEMISTRY, 2003, 75 (07) : 1584 - 1589
  • [70] Identification of phytochrome-interacting protein candidates in Arabidopsis thaliana by co-immunoprecipitation coupled with MALDI-TOF MS
    Phee, Bong-Kwan
    Shin, Dong Ho
    Cho, Jin-Hwan
    Kim, Seong-Hee
    Kim, Jeong-Il
    Lee, Youn-Hyung
    Jeon, Jong-Seong
    Bhoo, Seong Hee
    Hahn, Tae-Ryong
    [J]. PROTEOMICS, 2006, 6 (12) : 3671 - 3680