Cell entry and cAMP imaging of anthrax edema toxin.

The entry and enzymatic activity of the anthrax edema factor (EF) in different cell types was studied by monitoring EF-induced changes in intracellular cAMP with biochemical and microscopic methods. cAMP was imaged in live cells, transfected with a fluorescence resonance energy transfer biosensor ba...

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Автори: Dal Molin, F, Tonello, F, Ladant, D, Zornetta, I, Zamparo, I, Di Benedetto, G, Zaccolo, M, Montecucco, C
Формат: Journal article
Мова:English
Опубліковано: 2006
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author Dal Molin, F
Tonello, F
Ladant, D
Zornetta, I
Zamparo, I
Di Benedetto, G
Zaccolo, M
Montecucco, C
author_facet Dal Molin, F
Tonello, F
Ladant, D
Zornetta, I
Zamparo, I
Di Benedetto, G
Zaccolo, M
Montecucco, C
author_sort Dal Molin, F
collection OXFORD
description The entry and enzymatic activity of the anthrax edema factor (EF) in different cell types was studied by monitoring EF-induced changes in intracellular cAMP with biochemical and microscopic methods. cAMP was imaged in live cells, transfected with a fluorescence resonance energy transfer biosensor based on the protein kinase A regulatory and catalytic subunits fused to CFP and YFP, respectively. The cAMP biosensor was located either in the cytosol or was membrane-bound owing to the addition of a tag determining its myristoylation/palmitoylation. Real-time imaging of cells expressing the cAMP biosensors provided the time course of EF catalytic activity and an indication of its subcellular localization. Bafilomycin A1, an inhibitor of the vacuolar ATPase proton pump, completely prevented EF activity, even when added long after the toxin. The time course of appearance of the adenylate cyclase activity and of bafilomycin A1 action suggests that EF enters the cytosol from late endosomes. EF remains associated to these compartments and its activity shows a perinuclear localization generating intracellular cAMP concentration gradients from the cell centre to the periphery.
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spelling oxford-uuid:5d5967e2-84db-4fdd-9823-c8966d944b932022-03-26T17:33:54ZCell entry and cAMP imaging of anthrax edema toxin.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:5d5967e2-84db-4fdd-9823-c8966d944b93EnglishSymplectic Elements at Oxford2006Dal Molin, FTonello, FLadant, DZornetta, IZamparo, IDi Benedetto, GZaccolo, MMontecucco, CThe entry and enzymatic activity of the anthrax edema factor (EF) in different cell types was studied by monitoring EF-induced changes in intracellular cAMP with biochemical and microscopic methods. cAMP was imaged in live cells, transfected with a fluorescence resonance energy transfer biosensor based on the protein kinase A regulatory and catalytic subunits fused to CFP and YFP, respectively. The cAMP biosensor was located either in the cytosol or was membrane-bound owing to the addition of a tag determining its myristoylation/palmitoylation. Real-time imaging of cells expressing the cAMP biosensors provided the time course of EF catalytic activity and an indication of its subcellular localization. Bafilomycin A1, an inhibitor of the vacuolar ATPase proton pump, completely prevented EF activity, even when added long after the toxin. The time course of appearance of the adenylate cyclase activity and of bafilomycin A1 action suggests that EF enters the cytosol from late endosomes. EF remains associated to these compartments and its activity shows a perinuclear localization generating intracellular cAMP concentration gradients from the cell centre to the periphery.
spellingShingle Dal Molin, F
Tonello, F
Ladant, D
Zornetta, I
Zamparo, I
Di Benedetto, G
Zaccolo, M
Montecucco, C
Cell entry and cAMP imaging of anthrax edema toxin.
title Cell entry and cAMP imaging of anthrax edema toxin.
title_full Cell entry and cAMP imaging of anthrax edema toxin.
title_fullStr Cell entry and cAMP imaging of anthrax edema toxin.
title_full_unstemmed Cell entry and cAMP imaging of anthrax edema toxin.
title_short Cell entry and cAMP imaging of anthrax edema toxin.
title_sort cell entry and camp imaging of anthrax edema toxin
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