Literature DB >> 14595367

FRET imaging.

Elizabeth A Jares-Erijman1, Thomas M Jovin.   

Abstract

Förster (or Fluorescence) Resonance Energy Transfer (FRET) is unique in generating fluorescence signals sensitive to molecular conformation, association, and separation in the 1-10 nm range. We introduce a revised photophysical framework for the phenomenon and provide a systematic catalog of FRET techniques adapted to imaging systems, including new approaches proposed as suitable prospects for implementation. Applications extending from a single molecule to live cells will benefit from multidimensional microscopy techniques, particularly those adapted for optical sectioning and incorporating new algorithms for resolving the component contributions to images of complex molecular systems.

Mesh:

Substances:

Year:  2003        PMID: 14595367     DOI: 10.1038/nbt896

Source DB:  PubMed          Journal:  Nat Biotechnol        ISSN: 1087-0156            Impact factor:   54.908


  381 in total

1.  Dual-channel photobleaching FRET microscopy for improved resolution of protein association states in living cells.

Authors:  Andrew H A Clayton; Nectarios Klonis; Stephen H Cody; Edouard C Nice
Journal:  Eur Biophys J       Date:  2004-06-30       Impact factor: 1.733

2.  Tuning upconversion through energy migration in core-shell nanoparticles.

Authors:  Feng Wang; Renren Deng; Juan Wang; Qingxiao Wang; Yu Han; Haomiao Zhu; Xueyuan Chen; Xiaogang Liu
Journal:  Nat Mater       Date:  2011-10-23       Impact factor: 43.841

3.  Systematic control of protein interactions for systems biology.

Authors:  Nitin Bhardwaj; Declan Clarke; Mark Gerstein
Journal:  Proc Natl Acad Sci U S A       Date:  2011-12-12       Impact factor: 11.205

4.  Imaging protein activity in live embryos using fluorescence resonance energy transfer biosensors.

Authors:  Elena Kardash; Jan Bandemer; Erez Raz
Journal:  Nat Protoc       Date:  2011-11-03       Impact factor: 13.491

Review 5.  Monitoring protein interactions in living cells with fluorescence lifetime imaging microscopy.

Authors:  Yuansheng Sun; Nicole M Hays; Ammasi Periasamy; Michael W Davidson; Richard N Day
Journal:  Methods Enzymol       Date:  2012       Impact factor: 1.600

6.  Two different binding modes of α-synuclein to lipid vesicles depending on its aggregation state.

Authors:  Tobias Högen; Johannes Levin; Felix Schmidt; Mario Caruana; Neville Vassallo; Hans Kretzschmar; Kai Bötzel; Frits Kamp; Armin Giese
Journal:  Biophys J       Date:  2012-04-03       Impact factor: 4.033

7.  Induced heterodimerization and purification of two target proteins by a synthetic coiled-coil tag.

Authors:  Jesus Fernandez-Rodriguez; Thomas C Marlovits
Journal:  Protein Sci       Date:  2012-02-23       Impact factor: 6.725

Review 8.  Proteins on the move: insights gained from fluorescent protein technologies.

Authors:  Atsushi Miyawaki
Journal:  Nat Rev Mol Cell Biol       Date:  2011-09-23       Impact factor: 94.444

9.  Monitoring multiple distances within a single molecule using switchable FRET.

Authors:  Stephan Uphoff; Seamus J Holden; Ludovic Le Reste; Javier Periz; Sebastian van de Linde; Mike Heilemann; Achillefs N Kapanidis
Journal:  Nat Methods       Date:  2010-09-05       Impact factor: 28.547

10.  Coclustering of ErbB1 and ErbB2 revealed by FRET-sensitized acceptor bleaching.

Authors:  Agnes Szabó; János Szöllosi; Peter Nagy
Journal:  Biophys J       Date:  2010-07-07       Impact factor: 4.033

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.