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PMID: 19150604 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Imaging protein-protein interactions in plant cells by bimolecular fluorescence complementation assay.

Trends in plant science ·Vol. 14 ·No. 2 ·2009-02-00 ·Pages 59-63

Weinthal D, Tzfira T

Abstract

The bimolecular fluorescence complementation (BiFC) assay is based on the reconstruction of a fluorescent signal upon the interaction of two protein partners fused to two non-fluorescent fragments of an otherwise fluorescent protein. Interacting partners are typically tagged to fragments of the yellow fluorescent protein, but the use of other fluorescent proteins has been reported. By combining fragments of different types of fluorescent proteins, it is possible not only to detect pairwise protein-protein interaction but also to study the formation of multiprotein complexes in living cells. As we discuss here, a multicolor BiFC set of vectors has been recently deployed for visualizing the simultaneous formation of alternative protein kinase and calcium sensor complexes in living plant cells. This proof-of-concept report and the vectors that have been developed are an important addition to the sets of tools that are useful for analysing multiprotein complexes in plant cells.

MeSH Terms
Fluorescence Genetic Complementation Test/methods Plant Cells Plant Proteins/metabolism Plants/metabolism Protein Binding
Chemicals
Plant Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Weinthal Dan
Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109-1048, USA.
Tzfira Tzvi
Article Info
Journal
Trends in plant science
Abbr.
Trends Plant Sci
ISSN
1360-1385
Published
2009-02-00
Epub
2009-00-15
Pages
59-63
Language
English
Region
England
NLM ID
9890299
Subset
IM
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