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photoreversible fluorescent protein iLOV outperforms GFP as a reporter of plant virus infection
by
Kaiserli, Eirini
, Garcia-Mata, Carlos
, Savenkov, Eugene I
, Chapman, Sean
, Oparka, Karl J
, Christie, John M
, Faulkner, Christine
, Roberts, Alison G
in
Animals
/ Arabidopsis thaliana
/ Biological Sciences
/ cell lines
/ Cells
/ confocal microscopy
/ Cryptochromes
/ Directed Molecular Evolution
/ DNA shuffling
/ Flavins - chemistry
/ Flavoproteins - analysis
/ Flavoproteins - genetics
/ Flavoproteins - metabolism
/ Flavoproteins - radiation effects
/ Fluorescence
/ Gene expression
/ Genes, Reporter
/ Genetic Engineering
/ Genomics
/ Green Fluorescent Proteins - analysis
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Green Fluorescent Proteins - radiation effects
/ infection
/ Infections
/ Inoculation
/ Lesions
/ Luminescent Proteins - analysis
/ Luminescent Proteins - genetics
/ Luminescent Proteins - metabolism
/ Luminescent Proteins - radiation effects
/ Microscopy, Confocal
/ Microscopy, Fluorescence
/ Nicotiana benthamiana
/ Nicotiana tabacum
/ Oxygen - metabolism
/ Photobleaching
/ Photochemistry
/ photoreceptors
/ phototropin
/ Plant cells
/ Plant pathology
/ Plant viruses
/ Plant Viruses - genetics
/ Plant Viruses - metabolism
/ Plant Viruses - physiology
/ Plants - virology
/ Polymerase chain reaction
/ Proteins
/ Recombinant Fusion Proteins
/ recombinant proteins
/ reporter genes
/ Studies
/ tobacco
/ Tobacco mosaic virus
/ Tobacco Mosaic Virus - genetics
/ Tobacco Mosaic Virus - physiology
/ transgenes
/ Viral Proteins - analysis
/ Viral Proteins - genetics
/ Viral Proteins - metabolism
/ Viral Proteins - radiation effects
/ Viruses
2008
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photoreversible fluorescent protein iLOV outperforms GFP as a reporter of plant virus infection
by
Kaiserli, Eirini
, Garcia-Mata, Carlos
, Savenkov, Eugene I
, Chapman, Sean
, Oparka, Karl J
, Christie, John M
, Faulkner, Christine
, Roberts, Alison G
in
Animals
/ Arabidopsis thaliana
/ Biological Sciences
/ cell lines
/ Cells
/ confocal microscopy
/ Cryptochromes
/ Directed Molecular Evolution
/ DNA shuffling
/ Flavins - chemistry
/ Flavoproteins - analysis
/ Flavoproteins - genetics
/ Flavoproteins - metabolism
/ Flavoproteins - radiation effects
/ Fluorescence
/ Gene expression
/ Genes, Reporter
/ Genetic Engineering
/ Genomics
/ Green Fluorescent Proteins - analysis
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Green Fluorescent Proteins - radiation effects
/ infection
/ Infections
/ Inoculation
/ Lesions
/ Luminescent Proteins - analysis
/ Luminescent Proteins - genetics
/ Luminescent Proteins - metabolism
/ Luminescent Proteins - radiation effects
/ Microscopy, Confocal
/ Microscopy, Fluorescence
/ Nicotiana benthamiana
/ Nicotiana tabacum
/ Oxygen - metabolism
/ Photobleaching
/ Photochemistry
/ photoreceptors
/ phototropin
/ Plant cells
/ Plant pathology
/ Plant viruses
/ Plant Viruses - genetics
/ Plant Viruses - metabolism
/ Plant Viruses - physiology
/ Plants - virology
/ Polymerase chain reaction
/ Proteins
/ Recombinant Fusion Proteins
/ recombinant proteins
/ reporter genes
/ Studies
/ tobacco
/ Tobacco mosaic virus
/ Tobacco Mosaic Virus - genetics
/ Tobacco Mosaic Virus - physiology
/ transgenes
/ Viral Proteins - analysis
/ Viral Proteins - genetics
/ Viral Proteins - metabolism
/ Viral Proteins - radiation effects
/ Viruses
2008
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photoreversible fluorescent protein iLOV outperforms GFP as a reporter of plant virus infection
by
Kaiserli, Eirini
, Garcia-Mata, Carlos
, Savenkov, Eugene I
, Chapman, Sean
, Oparka, Karl J
, Christie, John M
, Faulkner, Christine
, Roberts, Alison G
in
Animals
/ Arabidopsis thaliana
/ Biological Sciences
/ cell lines
/ Cells
/ confocal microscopy
/ Cryptochromes
/ Directed Molecular Evolution
/ DNA shuffling
/ Flavins - chemistry
/ Flavoproteins - analysis
/ Flavoproteins - genetics
/ Flavoproteins - metabolism
/ Flavoproteins - radiation effects
/ Fluorescence
/ Gene expression
/ Genes, Reporter
/ Genetic Engineering
/ Genomics
/ Green Fluorescent Proteins - analysis
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Green Fluorescent Proteins - radiation effects
/ infection
/ Infections
/ Inoculation
/ Lesions
/ Luminescent Proteins - analysis
/ Luminescent Proteins - genetics
/ Luminescent Proteins - metabolism
/ Luminescent Proteins - radiation effects
/ Microscopy, Confocal
/ Microscopy, Fluorescence
/ Nicotiana benthamiana
/ Nicotiana tabacum
/ Oxygen - metabolism
/ Photobleaching
/ Photochemistry
/ photoreceptors
/ phototropin
/ Plant cells
/ Plant pathology
/ Plant viruses
/ Plant Viruses - genetics
/ Plant Viruses - metabolism
/ Plant Viruses - physiology
/ Plants - virology
/ Polymerase chain reaction
/ Proteins
/ Recombinant Fusion Proteins
/ recombinant proteins
/ reporter genes
/ Studies
/ tobacco
/ Tobacco mosaic virus
/ Tobacco Mosaic Virus - genetics
/ Tobacco Mosaic Virus - physiology
/ transgenes
/ Viral Proteins - analysis
/ Viral Proteins - genetics
/ Viral Proteins - metabolism
/ Viral Proteins - radiation effects
/ Viruses
2008
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photoreversible fluorescent protein iLOV outperforms GFP as a reporter of plant virus infection
Journal Article
photoreversible fluorescent protein iLOV outperforms GFP as a reporter of plant virus infection
2008
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Overview
Fluorescent proteins (FPs) based on green fluorescent protein (GFP) are widely used throughout cell biology to study protein dynamics, and have extensive use as reporters of virus infection and spread. However, FP-tagging of viruses is limited by the constraints of viral genome size resulting in FP loss through recombination events. To overcome this, we have engineered a smaller ([almost equal to]10 kDa) flavin-based alternative to GFP ([almost equal to]25 kDa) derived from the light, oxygen or voltage-sensing (LOV) domain of the plant blue light receptor, phototropin. Molecular evolution and Tobacco mosaic virus (TMV)-based expression screening produced LOV variants with improved fluorescence and photostability in planta. One variant in particular, designated iLOV, possessed photophysical properties that made it ideally suited as a reporter of subcellular protein localization in both plant and mammalian cells. Moreover, iLOV fluorescence was found to recover spontaneously after photobleaching and displayed an intrinsic photochemistry conferring advantages over GFP-based FPs. When expressed either as a cytosolic protein or as a viral protein fusion, iLOV functioned as a superior reporter to GFP for monitoring local and systemic infections of plant RNA viruses. iLOV, therefore, offers greater utility in FP-tagging of viral gene products and represents a viable alternative where functional protein expression is limited by steric constraints or genome size.
Publisher
National Academy of Sciences,National Acad Sciences
Subject
/ Cells
/ Directed Molecular Evolution
/ Flavoproteins - radiation effects
/ Genomics
/ Green Fluorescent Proteins - analysis
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Green Fluorescent Proteins - radiation effects
/ Lesions
/ Luminescent Proteins - analysis
/ Luminescent Proteins - genetics
/ Luminescent Proteins - metabolism
/ Luminescent Proteins - radiation effects
/ Proteins
/ Studies
/ tobacco
/ Tobacco Mosaic Virus - genetics
/ Tobacco Mosaic Virus - physiology
/ Viral Proteins - radiation effects
/ Viruses
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