Literature DB >> 18228482

Visualization of protein interactions in living cells using bimolecular fluorescence complementation (BiFC) analysis.

Chang-Deng Hu1, Asya V Grinberg, Tom K Kerppola.   

Abstract

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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Year:  2006        PMID: 18228482     DOI: 10.1002/0471143030.cb2103s29

Source DB:  PubMed          Journal:  Curr Protoc Cell Biol        ISSN: 1934-2616


  32 in total

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Authors:  Jeffrey J Hodgson; Basil M Arif; Peter J Krell
Journal:  J Virol       Date:  2011-02-02       Impact factor: 5.103

2.  Visualizing protein-RNA interactions inside cells by fluorescence resonance energy transfer.

Authors:  Mike Lorenz
Journal:  RNA       Date:  2008-11-25       Impact factor: 4.942

Review 3.  Fluorescent and bioluminescent protein-fragment complementation assays in the study of G protein-coupled receptor oligomerization and signaling.

Authors:  Pierre-Alexandre Vidi; Val J Watts
Journal:  Mol Pharmacol       Date:  2009-01-13       Impact factor: 4.436

4.  The Survival of Motor Neuron Protein Acts as a Molecular Chaperone for mRNP Assembly.

Authors:  Paul G Donlin-Asp; Claudia Fallini; Jazmin Campos; Ching-Chieh Chou; Megan E Merritt; Han C Phan; Gary J Bassell; Wilfried Rossoll
Journal:  Cell Rep       Date:  2017-02-14       Impact factor: 9.423

5.  Role of interactions between Autographa californica multiple nucleopolyhedrovirus procathepsin and chitinase chitin-binding or active-site domains in viral cathepsin processing.

Authors:  Jeffrey J Hodgson; Basil M Arif; Peter J Krell
Journal:  J Virol       Date:  2013-01-09       Impact factor: 5.103

6.  Visualization of positive transcription elongation factor b (P-TEFb) activation in living cells.

Authors:  Koh Fujinaga; Zeping Luo; Fred Schaufele; B Matija Peterlin
Journal:  J Biol Chem       Date:  2014-12-09       Impact factor: 5.157

7.  Bimolecular Fluorescence Complementation (BiFC) and Multiplexed Imaging of Protein-Protein Interactions in Human Living Cells.

Authors:  Yunlong Jia; Françoise Bleicher; Jonathan Reboulet; Samir Merabet
Journal:  Methods Mol Biol       Date:  2021

8.  Plant protein-protein interaction network and interactome.

Authors:  Yixiang Zhang; Peng Gao; Joshua S Yuan
Journal:  Curr Genomics       Date:  2010-03       Impact factor: 2.236

9.  Bacterial effector binding to ribosomal protein s3 subverts NF-kappaB function.

Authors:  Xiaofei Gao; Fengyi Wan; Kristina Mateo; Eduardo Callegari; Dan Wang; Wanyin Deng; Jose Puente; Feng Li; Michael S Chaussee; B Brett Finlay; Michael J Lenardo; Philip R Hardwidge
Journal:  PLoS Pathog       Date:  2009-12-24       Impact factor: 6.823

10.  Zinc coordination is required for and regulates transcription activation by Epstein-Barr nuclear antigen 1.

Authors:  Siddhesh Aras; Gyanendra Singh; Kenneth Johnston; Timothy Foster; Ashok Aiyar
Journal:  PLoS Pathog       Date:  2009-06-12       Impact factor: 6.823

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