Literature DB >> 19118691

Chapter 22: Quantitation of protein-protein interactions: confocal FRET microscopy.

Ammasi Periasamy1, Horst Wallrabe, Ye Chen, Margarida Barroso.   

Abstract

Förster resonance energy transfer (FRET) is an effective and high resolution method to monitor protein-protein interactions in live or fixed specimens. FRET can be used to estimate the distance between interacting protein molecules in vivo or in vitro using laser-scanning confocal FRET microscopy. The spectral overlap of donor and acceptor-essential for FRET-also generates a contamination of the FRET signal, which should be removed in order to carry out quantitative data analysis with confidence. Quantitative FRET data analysis addresses the wealth of information contained in the data set, once optimized FRET imaging has been completed. In this chapter, we describe step-by-step what the issues are in quantitative FRET data analysis, using membrane receptor trafficking and organization as an example. The assays described are applicable to many other biological applications.

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Year:  2008        PMID: 19118691     DOI: 10.1016/S0091-679X(08)00622-5

Source DB:  PubMed          Journal:  Methods Cell Biol        ISSN: 0091-679X            Impact factor:   1.441


  29 in total

1.  Automated selection of regions of interest for intensity-based FRET analysis of transferrin endocytic trafficking in normal vs. cancer cells.

Authors:  Ronak Talati; Andrew Vanderpoel; Amina Eladdadi; Kate Anderson; Ken Abe; Margarida Barroso
Journal:  Methods       Date:  2013-08-28       Impact factor: 3.608

2.  Construction, imaging, and analysis of FRET-based tension sensors in living cells.

Authors:  Andrew S LaCroix; Katheryn E Rothenberg; Matthew E Berginski; Aarti N Urs; Brenton D Hoffman
Journal:  Methods Cell Biol       Date:  2015-01-08       Impact factor: 1.441

3.  Dynamics and molecular interactions of linker of nucleoskeleton and cytoskeleton (LINC) complex proteins.

Authors:  Cecilia Ostlund; Eric S Folker; Jason C Choi; Edgar R Gomes; Gregg G Gundersen; Howard J Worman
Journal:  J Cell Sci       Date:  2009-10-20       Impact factor: 5.285

4.  Interaction of human biliverdin reductase with Akt/protein kinase B and phosphatidylinositol-dependent kinase 1 regulates glycogen synthase kinase 3 activity: a novel mechanism of Akt activation.

Authors:  Tihomir Miralem; Nicole Lerner-Marmarosh; Peter E M Gibbs; Jermaine L Jenkins; Chelsea Heimiller; Mahin D Maines
Journal:  FASEB J       Date:  2016-05-10       Impact factor: 5.191

Review 5.  Quantum dots in cell biology.

Authors:  Margarida M Barroso
Journal:  J Histochem Cytochem       Date:  2011-03       Impact factor: 2.479

6.  Investigating protein-protein interactions in living cells using fluorescence lifetime imaging microscopy.

Authors:  Yuansheng Sun; Richard N Day; Ammasi Periasamy
Journal:  Nat Protoc       Date:  2011-08-11       Impact factor: 13.491

7.  Single Proteoliposome High-Content Analysis Reveals Differences in the Homo-Oligomerization of GPCRs.

Authors:  Samuel M Walsh; Signe Mathiasen; Sune M Christensen; Jonathan F Fay; Christopher King; Davide Provasi; Ernesto Borrero; Søren G F Rasmussen; Juan Jose Fung; Marta Filizola; Kalina Hristova; Brian Kobilka; David L Farrens; Dimitrios Stamou
Journal:  Biophys J       Date:  2018-07-17       Impact factor: 4.033

8.  Reduced temporal sampling effect on accuracy of time-domain fluorescence lifetime Förster resonance energy transfer.

Authors:  Travis Omer; Lingling Zhao; Xavier Intes; Juergen Hahn
Journal:  J Biomed Opt       Date:  2014-08       Impact factor: 3.170

9.  Lamina-associated polypeptide-1 interacts with the muscular dystrophy protein emerin and is essential for skeletal muscle maintenance.

Authors:  Ji-Yeon Shin; Iván Méndez-López; Yuexia Wang; Arthur P Hays; Kurenai Tanji; Jay H Lefkowitch; P Christian Schulze; Howard J Worman; William T Dauer
Journal:  Dev Cell       Date:  2013-09-19       Impact factor: 12.270

10.  Fluorescent fusion proteins of soluble guanylyl cyclase indicate proximity of the heme nitric oxide domain and catalytic domain.

Authors:  Tobias Haase; Nadine Haase; Jan Robert Kraehling; Soenke Behrends
Journal:  PLoS One       Date:  2010-07-15       Impact factor: 3.240

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