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Distribution and Structure Analysis of Fibril-Forming Peptides Focusing on Concentration Dependency

[Image: see text] We focus on the concentration dependency of fibril-forming peptides, which have the potential of aggregation by themselves. In this study, we performed replica-exchange molecular dynamics simulations of Lys-Phe-Phe-Glu (KFFE) fragments, which are known to form fibrils in experiment...

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Autores principales: Sakae, Yoshitake, Kawasaki, Takeshi, Okamoto, Yuko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975544/
https://www.ncbi.nlm.nih.gov/pubmed/35382341
http://dx.doi.org/10.1021/acsomega.1c04960
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author Sakae, Yoshitake
Kawasaki, Takeshi
Okamoto, Yuko
author_facet Sakae, Yoshitake
Kawasaki, Takeshi
Okamoto, Yuko
author_sort Sakae, Yoshitake
collection PubMed
description [Image: see text] We focus on the concentration dependency of fibril-forming peptides, which have the potential of aggregation by themselves. In this study, we performed replica-exchange molecular dynamics simulations of Lys-Phe-Phe-Glu (KFFE) fragments, which are known to form fibrils in experiments under different concentration environments. The analysis by static structure factors suggested that the density fluctuation of the KFFE fragments becomes large as the concentration increases. It was also found that the number of β-structures and oligomers also increases under a high concentration environment. Hence, a high concentration environment of fibril-forming peptides is likely to cause protein aggregation.
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spelling pubmed-89755442022-04-04 Distribution and Structure Analysis of Fibril-Forming Peptides Focusing on Concentration Dependency Sakae, Yoshitake Kawasaki, Takeshi Okamoto, Yuko ACS Omega [Image: see text] We focus on the concentration dependency of fibril-forming peptides, which have the potential of aggregation by themselves. In this study, we performed replica-exchange molecular dynamics simulations of Lys-Phe-Phe-Glu (KFFE) fragments, which are known to form fibrils in experiments under different concentration environments. The analysis by static structure factors suggested that the density fluctuation of the KFFE fragments becomes large as the concentration increases. It was also found that the number of β-structures and oligomers also increases under a high concentration environment. Hence, a high concentration environment of fibril-forming peptides is likely to cause protein aggregation. American Chemical Society 2022-03-14 /pmc/articles/PMC8975544/ /pubmed/35382341 http://dx.doi.org/10.1021/acsomega.1c04960 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Sakae, Yoshitake
Kawasaki, Takeshi
Okamoto, Yuko
Distribution and Structure Analysis of Fibril-Forming Peptides Focusing on Concentration Dependency
title Distribution and Structure Analysis of Fibril-Forming Peptides Focusing on Concentration Dependency
title_full Distribution and Structure Analysis of Fibril-Forming Peptides Focusing on Concentration Dependency
title_fullStr Distribution and Structure Analysis of Fibril-Forming Peptides Focusing on Concentration Dependency
title_full_unstemmed Distribution and Structure Analysis of Fibril-Forming Peptides Focusing on Concentration Dependency
title_short Distribution and Structure Analysis of Fibril-Forming Peptides Focusing on Concentration Dependency
title_sort distribution and structure analysis of fibril-forming peptides focusing on concentration dependency
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975544/
https://www.ncbi.nlm.nih.gov/pubmed/35382341
http://dx.doi.org/10.1021/acsomega.1c04960
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