4.7 Review

Fluorescence resonance energy transfer-based technologies in the study of protein-protein interactions at the cell surface

Journal

METHODS
Volume 57, Issue 4, Pages 467-472

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymeth.2012.05.007

Keywords

FRET; Protein-protein interactions; Cell surface; GPCR; TIRF; SNAP; TR-FRET

Funding

  1. Ministerio de Ciencia e Innovacion [SAF2011-24779, CSD2008-00005]
  2. Catalan Institution for Research and Advanced Studies
  3. CAPES [BEX 6425/10-0]

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Understanding of the molecular mechanisms of protein-protein interactions (PPIs) at the cell surface of living cells is fundamental to comprehend the functional meaning of a large number of cellular processes. Here we discuss how new methodological strategies derived from non-invasive fluorescence-based approaches (i.e. fluorescence resonance energy transfer, FRET) have been successfully developed to characterize plasma membrane PPIs. Importantly, these technologies alone - or in concert with complementary methods (i.e. SNAP-tag/TR-FRET, TIRF/FRET) - can become extremely powerful approaches for visualizing cell surface PPIs, even between more than two proteins and also in native tissues. Interestingly, these methods would also be relevant in drug discovery in order to develop new high-throughput screening approaches or to identify new therapeutic targets. Accordingly, herein we provide a thorough assessment on all biotechnological aspects, including strengths and weaknesses, of these fluorescence-based methodologies when applied in the study of PPIs occurring at the cell surface of living cells. (C) 2012 Elsevier Inc. All rights reserved.

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