Literature DB >> 23529432

Förster resonance energy transfer-based imaging at the cell surface of live cells.

Sonya M Bierbower1, Mark S Shapiro.   

Abstract

Understanding the molecular mechanisms of protein-protein interactions at the cell surface of living cells is fundamental to identifying the nature of cellular processes. Here, we discuss how fluorescence-based approaches have been successfully developed to visualize protein-protein interactions in living cells. Förster resonance energy transfer (FRET) is unique in generating fluorescence signals between proteins that are highly spatially sensitive. Furthermore, total internal reflectance fluorescence (TIRF) microscopy combined with FRET is a robust technique used to assay protein/protein interactions and the functionality of proteins assembled at the cell surface membrane.

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Year:  2013        PMID: 23529432      PMCID: PMC4086792          DOI: 10.1007/978-1-62703-351-0_16

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  10 in total

1.  Fluorescence resonance energy transfer imaging microscopy.

Authors:  Victoria E Centonze; Mao Sun; Atsushi Masuda; Hans Gerritsen; Brian Herman
Journal:  Methods Enzymol       Date:  2003       Impact factor: 1.600

Review 2.  FRET imaging.

Authors:  Elizabeth A Jares-Erijman; Thomas M Jovin
Journal:  Nat Biotechnol       Date:  2003-11       Impact factor: 54.908

3.  Evidence for association of GABA(B) receptors with Kir3 channels and regulators of G protein signalling (RGS4) proteins.

Authors:  Catherine E Fowler; Prafulla Aryal; Ka Fai Suen; Paul A Slesinger
Journal:  J Physiol       Date:  2006-12-21       Impact factor: 5.182

4.  GIRK channel activation involves a local rearrangement of a preformed G protein channel complex.

Authors:  Inbal Riven; Shachar Iwanir; Eitan Reuveny
Journal:  Neuron       Date:  2006-09-07       Impact factor: 17.173

Review 5.  Fluorescence energy transfer as a spectroscopic ruler.

Authors:  L Stryer
Journal:  Annu Rev Biochem       Date:  1978       Impact factor: 23.643

6.  Ca2+/calmodulin disrupts AKAP79/150 interactions with KCNQ (M-Type) K+ channels.

Authors:  Manjot Bal; Jie Zhang; Ciria C Hernandez; Oleg Zaika; Mark S Shapiro
Journal:  J Neurosci       Date:  2010-02-10       Impact factor: 6.167

7.  Imaging of single fluorescent molecules and individual ATP turnovers by single myosin molecules in aqueous solution.

Authors:  T Funatsu; Y Harada; M Tokunaga; K Saito; T Yanagida
Journal:  Nature       Date:  1995-04-06       Impact factor: 49.962

8.  Total internal inflection fluorescent microscopy.

Authors:  D Axelrod; N L Thompson; T P Burghardt
Journal:  J Microsc       Date:  1983-01       Impact factor: 1.758

9.  Calmodulin binding to M-type K+ channels assayed by TIRF/FRET in living cells.

Authors:  Manjot Bal; Oleg Zaika; Pamela Martin; Mark S Shapiro
Journal:  J Physiol       Date:  2008-03-13       Impact factor: 5.182

10.  Regulation of Kir2.1 channels by the Rho-GTPase, Rac1.

Authors:  Stephanie B Boyer; Paul A Slesinger; S V Penelope Jones
Journal:  J Cell Physiol       Date:  2009-02       Impact factor: 6.384

  10 in total
  3 in total

1.  Transgenic mice for cGMP imaging.

Authors:  Martin Thunemann; Lai Wen; Matthias Hillenbrand; Angelos Vachaviolos; Susanne Feil; Thomas Ott; Xiaoxing Han; Dai Fukumura; Rakesh K Jain; Michael Russwurm; Cor de Wit; Robert Feil
Journal:  Circ Res       Date:  2013-06-25       Impact factor: 17.367

Review 2.  Lasers in Live Cell Microscopy.

Authors:  Herbert Schneckenburger
Journal:  Int J Mol Sci       Date:  2022-04-30       Impact factor: 6.208

3.  Combining TIR and FRET in Molecular Test Systems.

Authors:  Herbert Schneckenburger; Petra Weber; Michael Wagner; Sandra Enderle; Bernd Kalthof; Linn Schneider; Claudia Herzog; Julian Weghuber; Peter Lanzerstorfer
Journal:  Int J Mol Sci       Date:  2019-02-02       Impact factor: 5.923

  3 in total

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