Literature DB >> 8578587

Understanding, improving and using green fluorescent proteins.

A B Cubitt1, R Heim, S R Adams, A E Boyd, L A Gross, R Y Tsien.   

Abstract

Green fluorescent proteins (GFPs) are presently attracting tremendous interest as the first general method to create strong visible fluorescence by purely molecular biological means. So far, they have been used as reporters of gene expression, tracers of cell lineage, and as fusion tags to monitor protein localization within living cells. However, the GFP originally cloned from the jellyfish Aequorea victoria has several nonoptimal properties including low brightness, a significant delay between protein synthesis and fluorescence development, and complex photoisomerization. Fortunately, the protein can be re-engineered by mutagenesis to ameliorate these deficiencies and shift the excitation and emission wavelengths, creating different colors and new applications.

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Year:  1995        PMID: 8578587     DOI: 10.1016/s0968-0004(00)89099-4

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


  269 in total

1.  Isolation, characterization, and localization of a capsule-associated gene, CAP10, of Cryptococcus neoformans.

Authors:  Y C Chang; K J Kwon-Chung
Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

2.  Real-time light-driven dynamics of the fluorescence emission in single green fluorescent protein molecules.

Authors:  M F Garcia-Parajo; G M Segers-Nolten; J A Veerman; J Greve; N F van Hulst
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-20       Impact factor: 11.205

3.  High rates of conjugation in bacterial biofilms as determined by quantitative in situ analysis.

Authors:  M Hausner; S Wuertz
Journal:  Appl Environ Microbiol       Date:  1999-08       Impact factor: 4.792

4.  Fluorescence correlation spectroscopy reveals fast optical excitation-driven intramolecular dynamics of yellow fluorescent proteins.

Authors:  P Schwille; S Kummer; A A Heikal; W E Moerner; W W Webb
Journal:  Proc Natl Acad Sci U S A       Date:  2000-01-04       Impact factor: 11.205

5.  Nuclear export signal located within theDNA-binding domain of the STAT1transcription factor.

Authors:  K M McBride; C McDonald; N C Reich
Journal:  EMBO J       Date:  2000-11-15       Impact factor: 11.598

Review 6.  Reporter gene vectors and assays.

Authors:  E Schenborn; D Groskreutz
Journal:  Mol Biotechnol       Date:  1999-11       Impact factor: 2.695

7.  Insertional mutagenesis based on illegitimate recombination in Schizosaccharomyces pombe.

Authors:  G Chua; L Taricani; W Stangle; P G Young
Journal:  Nucleic Acids Res       Date:  2000-06-01       Impact factor: 16.971

Review 8.  Measurement of bacterial gene expression in vivo.

Authors:  I Hautefort; J C Hinton
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-05-29       Impact factor: 6.237

9.  Identification of different emitting species in the red fluorescent protein DsRed by means of ensemble and single-molecule spectroscopy.

Authors:  M Cotlet; J Hofkens; S Habuchi; G Dirix; M Van Guyse; J Michiels; J Vanderleyden; F C De Schryver
Journal:  Proc Natl Acad Sci U S A       Date:  2001-11-27       Impact factor: 11.205

10.  Light-induced flickering of DsRed provides evidence for distinct and interconvertible fluorescent states.

Authors:  F Malvezzi-Campeggi; M Jahnz; K G Heinze; P Dittrich; P Schwille
Journal:  Biophys J       Date:  2001-09       Impact factor: 4.033

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