Visualizing protein interactions by bimolecular fluorescence complementation in Xenopus

Yasushi Saka, Anja I Hagemann, James C Smith

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

Bimolecular fluorescence complementation (BiFC) provides a simple and direct way to visualise protein-protein interactions in vivo and in real-time. In this article, we describe methods by which one can implement this approach in embryos of the South African claw-toed frog Xenopus laevis. We have made use of Venus, an improved version of yellow fluorescent protein (YFP), so as to achieve rapid detection of protein interactions. To suppress spontaneous interactions between the N- and C-terminal fragments of Venus, a point mutation (T153M) was introduced into the N-terminal fragment. We have used this reagent to monitor signalling by members of the transforming growth factor type beta family in cells of the Xenopus embryo.
Original languageEnglish
Pages (from-to)192-195
Number of pages4
JournalMethods
Volume45
Issue number3
Early online date27 Jun 2008
DOIs
Publication statusPublished - Jul 2008

Keywords

  • Activins
  • Animals
  • Embryo, Nonmammalian
  • Fluorescent Dyes
  • Gene Transfer Techniques
  • Kinetics
  • Luminescent Proteins
  • Microscopy, Fluorescence
  • Protein Interaction Mapping
  • Recombinant Fusion Proteins
  • Research Design
  • Smad2 Protein
  • Smad4 Protein
  • Xenopus Proteins
  • Xenopus laevis

Fingerprint Dive into the research topics of 'Visualizing protein interactions by bimolecular fluorescence complementation in Xenopus'. Together they form a unique fingerprint.

  • Cite this