Literature DB >> 7480149

Green fluorescent protein.

M Chalfie1.   

Abstract

Several bioluminescent coelenterates use a secondary fluorescent protein, the green fluorescent protein (GFP), in an energy transfer reaction to produce green light. The most studied of these proteins have been the GFPs from the jellyfish Aequorea victoria and the sea pansy Renilla reniformis. Although the proteins from these organisms are not identical, they are thought to have the same chromophore, which is derived from the primary amino acid sequence of GFP. The differences are thought to be due to changes in the protein environment of the chromophore. Recent interest in these molecules has arisen from the cloning of the Aequorea gfp cDNA and the demonstration that its expression in the absence of other Aequorea proteins results in a fluorescent product. This demonstration indicated that GFP could be used as a marker of gene expression and protein localization in living and fixed tissues. Bacterial, plant and animal (including mammalian) cells all express GFP. The heterologous expression of the gfp cDNA has also meant that it could be mutated to produce proteins with different fluorescent properties. Variants with more intense fluorescence or alterations in the excitation and emission spectra have been produced.

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Year:  1995        PMID: 7480149     DOI: 10.1111/j.1751-1097.1995.tb08712.x

Source DB:  PubMed          Journal:  Photochem Photobiol        ISSN: 0031-8655            Impact factor:   3.421


  56 in total

1.  The role of the 3-hydroxy 3-methylglutaryl coenzyme A reductase cytosolic domain in karmellae biogenesis.

Authors:  D A Profant; C J Roberts; A J Koning; R L Wright
Journal:  Mol Biol Cell       Date:  1999-10       Impact factor: 4.138

2.  Functional expression, quantification and cellular localization of the Hxt2 hexose transporter of Saccharomyces cerevisiae tagged with the green fluorescent protein.

Authors:  A L Kruckeberg; L Ye; J A Berden; K van Dam
Journal:  Biochem J       Date:  1999-04-15       Impact factor: 3.857

3.  Subnuclear distribution of topoisomerase I is linked to ongoing transcription and p53 status.

Authors:  Yinghui Mao; Issac R Mehl; Mark T Muller
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-22       Impact factor: 11.205

Review 4.  Use of reporter genes for optical measurements of neoplastic disease in vivo.

Authors:  C H Contag; D Jenkins; P R Contag; R S Negrin
Journal:  Neoplasia       Date:  2000 Jan-Apr       Impact factor: 5.715

5.  Immunolocalization of dinitrogenase reductase produced by Klebsiella pneumoniae in association with Zea mays L.

Authors:  M K Chelius; E W Triplett
Journal:  Appl Environ Microbiol       Date:  2000-02       Impact factor: 4.792

6.  How novel methods can help discover more information about foodborne pathogens.

Authors:  M W Griffiths
Journal:  Can J Infect Dis       Date:  2000-05

7.  Fluorescence complementation via EF-hand interactions.

Authors:  Ning Chen; Yiming Ye; Jin Zou; Shunyi Li; Siming Wang; Amy Martin; Robert Wohlhueter; Jenny J Yang
Journal:  J Biotechnol       Date:  2009-06-11       Impact factor: 3.307

8.  The first mutant of the Aequorea victoria green fluorescent protein that forms a red chromophore.

Authors:  Alexander S Mishin; Fedor V Subach; Ilia V Yampolsky; William King; Konstantin A Lukyanov; Vladislav V Verkhusha
Journal:  Biochemistry       Date:  2008-03-27       Impact factor: 3.162

9.  Use of the fluorescent timer DsRED-E5 as reporter to monitor dynamics of gene activity in plants.

Authors:  Rossana Mirabella; Carolien Franken; Gerard N M van der Krogt; Ton Bisseling; René Geurts
Journal:  Plant Physiol       Date:  2004-08       Impact factor: 8.340

10.  Dual-color fluorescence imaging in a nude mouse orthotopic glioma model.

Authors:  Xuepeng Zhang; Xuguang Zheng; Feng Jiang; Zheng Gang Zhang; Mark Katakowski; Michael Chopp
Journal:  J Neurosci Methods       Date:  2009-05-15       Impact factor: 2.390

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