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Visualization of Protein Interactions in Living Cells Using Bimolecular Fluorescence Complementation ( Bi FC ) Analysis
Author(s) -
Hu ChangDeng,
Grinberg Asya V.,
Kerppola Tom K.
Publication year - 2005
Publication title -
current protocols in cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.149
H-Index - 38
eISSN - 1934-2616
pISSN - 1934-2500
DOI - 10.1002/0471143030.cb2103s29
Subject(s) - bimolecular fluorescence complementation , complementation , protein–protein interaction , fluorescence , visualization , chemistry , fluorescent protein , green fluorescent protein , microbiology and biotechnology , biophysics , subcellular localization , biology , computer science , biochemistry , physics , cytoplasm , quantum mechanics , artificial intelligence , gene , phenotype
Protein interactions integrate stimuli from different signaling pathways and developmental programs. Bimolecular fluorescence complementation (BiFC) analysis has been developed for visualization of protein interactions in living cells. This approach is based on complementation between two fragments of a fluorescent protein when they are brought together by an interaction between proteins fused to the fragments, and it enables visualization of the subcellular locations of protein interactions in the normal cellular environment. It can be used for the analysis of many protein interactions and does not require information about the structures of the interaction partners. A multicolor BiFC approach has been developed for simultaneous visualization of interactions with multiple alternative partners in the same cell, based on complementation between fragments of engineered fluorescent proteins that produce bimolecular fluorescent complexes with distinct spectral characteristics. This enables comparison of subcellular distributions of different protein complexes in the same cell and allows analysis of competition between mutually exclusive interaction partners.

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