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A LEA model peptide protects the function of a red fluorescent protein in the dry state

We tested whether a short model peptide derived from a group 3 late embryogenesis abundant (G3LEA) protein is able to maintain the fluorescence activity of a red fluorescent protein, mKate2, in the dry state. The fluorescence intensity of mKate2 alone decreased gradually through repeated dehydration...

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Detalles Bibliográficos
Autores principales: Furuki, Takao, Niwa, Tatsuya, Taguchi, Hideki, Hatanaka, Rie, Kikawada, Takahiro, Sakurai, Minoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259040/
https://www.ncbi.nlm.nih.gov/pubmed/30519646
http://dx.doi.org/10.1016/j.bbrep.2018.11.006
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author Furuki, Takao
Niwa, Tatsuya
Taguchi, Hideki
Hatanaka, Rie
Kikawada, Takahiro
Sakurai, Minoru
author_facet Furuki, Takao
Niwa, Tatsuya
Taguchi, Hideki
Hatanaka, Rie
Kikawada, Takahiro
Sakurai, Minoru
author_sort Furuki, Takao
collection PubMed
description We tested whether a short model peptide derived from a group 3 late embryogenesis abundant (G3LEA) protein is able to maintain the fluorescence activity of a red fluorescent protein, mKate2, in the dry state. The fluorescence intensity of mKate2 alone decreased gradually through repeated dehydration-rehydration treatments. However, in the presence of the LEA model peptide, the peak intensity was maintained almost perfectly during such stress treatments, which implies that the three dimensional structure of the active site of mKate2 was protected even under severe desiccation conditions. For comparison, similar experiments were performed with other additives such as a native G3LEA protein, trehalose and BSA, all of whose protective abilities were lower than that of the LEA model peptide.
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spelling pubmed-62590402018-12-05 A LEA model peptide protects the function of a red fluorescent protein in the dry state Furuki, Takao Niwa, Tatsuya Taguchi, Hideki Hatanaka, Rie Kikawada, Takahiro Sakurai, Minoru Biochem Biophys Rep Research Article We tested whether a short model peptide derived from a group 3 late embryogenesis abundant (G3LEA) protein is able to maintain the fluorescence activity of a red fluorescent protein, mKate2, in the dry state. The fluorescence intensity of mKate2 alone decreased gradually through repeated dehydration-rehydration treatments. However, in the presence of the LEA model peptide, the peak intensity was maintained almost perfectly during such stress treatments, which implies that the three dimensional structure of the active site of mKate2 was protected even under severe desiccation conditions. For comparison, similar experiments were performed with other additives such as a native G3LEA protein, trehalose and BSA, all of whose protective abilities were lower than that of the LEA model peptide. Elsevier 2018-11-26 /pmc/articles/PMC6259040/ /pubmed/30519646 http://dx.doi.org/10.1016/j.bbrep.2018.11.006 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Furuki, Takao
Niwa, Tatsuya
Taguchi, Hideki
Hatanaka, Rie
Kikawada, Takahiro
Sakurai, Minoru
A LEA model peptide protects the function of a red fluorescent protein in the dry state
title A LEA model peptide protects the function of a red fluorescent protein in the dry state
title_full A LEA model peptide protects the function of a red fluorescent protein in the dry state
title_fullStr A LEA model peptide protects the function of a red fluorescent protein in the dry state
title_full_unstemmed A LEA model peptide protects the function of a red fluorescent protein in the dry state
title_short A LEA model peptide protects the function of a red fluorescent protein in the dry state
title_sort lea model peptide protects the function of a red fluorescent protein in the dry state
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259040/
https://www.ncbi.nlm.nih.gov/pubmed/30519646
http://dx.doi.org/10.1016/j.bbrep.2018.11.006
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