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Pressure and temperature dependence of fluorescence anisotropy of green fluorescent protein

We have studied the effect of high hydrostatic pressure and temperature on the steady state fluorescence anisotropy of Green Fluorescent Protein (GFP). We find that the fluorescence anisotropy of GFP at a constant temperature decreases with increasing pressure. At atmospheric pressure, anisotropy de...

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Detalles Bibliográficos
Autores principales: Kaur, Harpreet, Nguyen, Khanh, Kumar, Pradeep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984833/
https://www.ncbi.nlm.nih.gov/pubmed/35424839
http://dx.doi.org/10.1039/d1ra08977c
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author Kaur, Harpreet
Nguyen, Khanh
Kumar, Pradeep
author_facet Kaur, Harpreet
Nguyen, Khanh
Kumar, Pradeep
author_sort Kaur, Harpreet
collection PubMed
description We have studied the effect of high hydrostatic pressure and temperature on the steady state fluorescence anisotropy of Green Fluorescent Protein (GFP). We find that the fluorescence anisotropy of GFP at a constant temperature decreases with increasing pressure. At atmospheric pressure, anisotropy decreases with increasing temperature but exhibits a maximum with temperature for pressure larger than 20 MPa. The temperature corresponding to the maximum of anisotropy increases with increasing pressure. By taking into account of the rotational correlation time changes of GFP with the pressure–temperature dependent viscosity of the solvent, we argue that viscosity increase with pressure is not a major contributing factor to the decrease in anisotropy with pressure. The decrease of anisotropy with pressure may result from changes in H-bonding environment around the chromophore.
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spelling pubmed-89848332022-04-13 Pressure and temperature dependence of fluorescence anisotropy of green fluorescent protein Kaur, Harpreet Nguyen, Khanh Kumar, Pradeep RSC Adv Chemistry We have studied the effect of high hydrostatic pressure and temperature on the steady state fluorescence anisotropy of Green Fluorescent Protein (GFP). We find that the fluorescence anisotropy of GFP at a constant temperature decreases with increasing pressure. At atmospheric pressure, anisotropy decreases with increasing temperature but exhibits a maximum with temperature for pressure larger than 20 MPa. The temperature corresponding to the maximum of anisotropy increases with increasing pressure. By taking into account of the rotational correlation time changes of GFP with the pressure–temperature dependent viscosity of the solvent, we argue that viscosity increase with pressure is not a major contributing factor to the decrease in anisotropy with pressure. The decrease of anisotropy with pressure may result from changes in H-bonding environment around the chromophore. The Royal Society of Chemistry 2022-03-21 /pmc/articles/PMC8984833/ /pubmed/35424839 http://dx.doi.org/10.1039/d1ra08977c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Kaur, Harpreet
Nguyen, Khanh
Kumar, Pradeep
Pressure and temperature dependence of fluorescence anisotropy of green fluorescent protein
title Pressure and temperature dependence of fluorescence anisotropy of green fluorescent protein
title_full Pressure and temperature dependence of fluorescence anisotropy of green fluorescent protein
title_fullStr Pressure and temperature dependence of fluorescence anisotropy of green fluorescent protein
title_full_unstemmed Pressure and temperature dependence of fluorescence anisotropy of green fluorescent protein
title_short Pressure and temperature dependence of fluorescence anisotropy of green fluorescent protein
title_sort pressure and temperature dependence of fluorescence anisotropy of green fluorescent protein
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984833/
https://www.ncbi.nlm.nih.gov/pubmed/35424839
http://dx.doi.org/10.1039/d1ra08977c
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AT kumarpradeep pressureandtemperaturedependenceoffluorescenceanisotropyofgreenfluorescentprotein