7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Bimolecular fluorescence complementation (BiFC) analysis as a probe of protein interactions in living cells.

      1
      Annual review of biophysics
      Annual Reviews

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Protein interactions are a fundamental mechanism for the generation of biological regulatory specificity. The study of protein interactions in living cells is of particular significance because the interactions that occur in a particular cell depend on the full complement of proteins present in the cell and the external stimuli that influence the cell. Bimolecular fluorescence complementation (BiFC) analysis enables direct visualization of protein interactions in living cells. The BiFC assay is based on the association between two nonfluorescent fragments of a fluorescent protein when they are brought in proximity to each other by an interaction between proteins fused to the fragments. Numerous protein interactions have been visualized using the BiFC assay in many different cell types and organisms. The BiFC assay is technically straightforward and can be performed using standard molecular biology and cell culture reagents and a regular fluorescence microscope or flow cytometer.

          Related collections

          Author and article information

          Journal
          Annu Rev Biophys
          Annual review of biophysics
          Annual Reviews
          1936-122X
          1936-122X
          2008
          : 37
          Affiliations
          [1 ] Howard Hughes Medical Institute and Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan 48109-0650, USA. kerppola@umich.edu
          Article
          NIHMS163221
          10.1146/annurev.biophys.37.032807.125842
          2829326
          18573091
          c96e19f0-ee16-44eb-b8cc-bec8a73217ea
          History

          Comments

          Comment on this article