Literature DB >> 11780139

Imaging into the future: visualizing gene expression and protein interactions with fluorescent proteins.

Peter van Roessel1, Andrea H Brand.   

Abstract

Since its introduction into heterologous organisms as a marker of gene expression, the green fluorescent protein (GFP) has led a dramatic revolution in cell, developmental and neurobiology. By allowing breathtaking visualization of fluorescent fusion proteins as they move within and between cells, GFP has fundamentally transformed the spatial analysis of protein function. Now, new GFP technologies allow far more than simple observations of fusion protein localization. The growing family of fluorescent protein variants is enabling more sophisticated studies of protein function and illuminating wide-ranging processes from gene expression to second-messenger cascades and intercellular signalling. Together with advances in microscopy, new GFP-based experimental approaches are forging a second GFP revolution.

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Year:  2002        PMID: 11780139     DOI: 10.1038/ncb0102-e15

Source DB:  PubMed          Journal:  Nat Cell Biol        ISSN: 1465-7392            Impact factor:   28.824


  49 in total

1.  A biosensor for theophylline based on fluorescence detection of ligand-induced hammerhead ribozyme cleavage.

Authors:  Phillip T Sekella; David Rueda; Nils G Walter
Journal:  RNA       Date:  2002-10       Impact factor: 4.942

Review 2.  Strategies for identifying genes that play a role in spinal cord regeneration.

Authors:  M Wintzer; M Mladinic; D Lazarevic; C Casseler; A Cattaneo; J Nicholls
Journal:  J Anat       Date:  2004-01       Impact factor: 2.610

3.  [Experimental pilot study on surface activation of implants with liposomal vectors].

Authors:  M Thorwarth; K A Schlegel; J Wiltfang; S Rupprecht; J H Park
Journal:  Mund Kiefer Gesichtschir       Date:  2004-03-27

4.  RalA activation at nascent lamellipodia of epidermal growth factor-stimulated Cos7 cells and migrating Madin-Darby canine kidney cells.

Authors:  Akiyuki Takaya; Yusuke Ohba; Kazuo Kurokawa; Michiyuki Matsuda
Journal:  Mol Biol Cell       Date:  2004-03-19       Impact factor: 4.138

5.  Blind spectral decomposition of single-cell fluorescence by parallel factor analysis.

Authors:  Hideki Shirakawa; Shunichi Miyazaki
Journal:  Biophys J       Date:  2004-03       Impact factor: 4.033

6.  SOCS-1 localizes to the microtubule organizing complex-associated 20S proteasome.

Authors:  Bao Q Vuong; Teresita L Arenzana; Brian M Showalter; Julie Losman; X Peter Chen; Justin Mostecki; Alexander S Banks; Andre Limnander; Neil Fernandez; Paul B Rothman
Journal:  Mol Cell Biol       Date:  2004-10       Impact factor: 4.272

Review 7.  Imaging molecular interactions in living cells.

Authors:  Richard N Day; Fred Schaufele
Journal:  Mol Endocrinol       Date:  2005-03-10

Review 8.  Quantitative imaging of protein interactions in the cell nucleus.

Authors:  Ty C Voss; Ignacio A Demarco; Richard N Day
Journal:  Biotechniques       Date:  2005-03       Impact factor: 1.993

9.  [A lentivirus vector based assay system for quantitative detection of intracellular translocations of recombinant proteins].

Authors:  S P Chumakov; G V Il'inskaia; Iu E Kravchenko; E I Frolova; V S Prasolov; P M Chumakov
Journal:  Mol Biol (Mosk)       Date:  2008 Nov-Dec

Review 10.  The fluorescent protein palette: tools for cellular imaging.

Authors:  Richard N Day; Michael W Davidson
Journal:  Chem Soc Rev       Date:  2009-08-04       Impact factor: 54.564

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