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Nucleophilic Regulation of the Formation of Melanin-like Species by Amyloid Fibers

[Image: see text] This work examines the influences of amyloid fibers of hen egg white lysozyme (HEWL) on the formation of melanin-like species (MLS) with a rationally selected set of catechol derivatives. Catechol–amyloid interactions, which are central in melanogenesis, are complex and multifacete...

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Autores principales: Ha, Daehong, Kang, Kyungtae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8757343/
https://www.ncbi.nlm.nih.gov/pubmed/35036743
http://dx.doi.org/10.1021/acsomega.1c05399
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author Ha, Daehong
Kang, Kyungtae
author_facet Ha, Daehong
Kang, Kyungtae
author_sort Ha, Daehong
collection PubMed
description [Image: see text] This work examines the influences of amyloid fibers of hen egg white lysozyme (HEWL) on the formation of melanin-like species (MLS) with a rationally selected set of catechol derivatives. Catechol–amyloid interactions, which are central in melanogenesis, are complex and multifaceted, making them difficult to understand at the molecular level. The catechol derivatives are set to interact with HEWL amyloid fibers upon altering pH, and the resultant formation of MLS is characterized. For obtaining clues for the molecular mechanism by which HEWL fibers regulate the formation of MLS, putative intermolecular interactions are individually perturbed and their ramifications are analyzed. With the entire data set, we could conclude that the externally presented nucleophilic moieties of HEWL fibers play a major role in regulating the material and kinetic properties of MLS and their formation, respectively.
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spelling pubmed-87573432022-01-13 Nucleophilic Regulation of the Formation of Melanin-like Species by Amyloid Fibers Ha, Daehong Kang, Kyungtae ACS Omega [Image: see text] This work examines the influences of amyloid fibers of hen egg white lysozyme (HEWL) on the formation of melanin-like species (MLS) with a rationally selected set of catechol derivatives. Catechol–amyloid interactions, which are central in melanogenesis, are complex and multifaceted, making them difficult to understand at the molecular level. The catechol derivatives are set to interact with HEWL amyloid fibers upon altering pH, and the resultant formation of MLS is characterized. For obtaining clues for the molecular mechanism by which HEWL fibers regulate the formation of MLS, putative intermolecular interactions are individually perturbed and their ramifications are analyzed. With the entire data set, we could conclude that the externally presented nucleophilic moieties of HEWL fibers play a major role in regulating the material and kinetic properties of MLS and their formation, respectively. American Chemical Society 2021-12-20 /pmc/articles/PMC8757343/ /pubmed/35036743 http://dx.doi.org/10.1021/acsomega.1c05399 Text en © 2021 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 Ha, Daehong
Kang, Kyungtae
Nucleophilic Regulation of the Formation of Melanin-like Species by Amyloid Fibers
title Nucleophilic Regulation of the Formation of Melanin-like Species by Amyloid Fibers
title_full Nucleophilic Regulation of the Formation of Melanin-like Species by Amyloid Fibers
title_fullStr Nucleophilic Regulation of the Formation of Melanin-like Species by Amyloid Fibers
title_full_unstemmed Nucleophilic Regulation of the Formation of Melanin-like Species by Amyloid Fibers
title_short Nucleophilic Regulation of the Formation of Melanin-like Species by Amyloid Fibers
title_sort nucleophilic regulation of the formation of melanin-like species by amyloid fibers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8757343/
https://www.ncbi.nlm.nih.gov/pubmed/35036743
http://dx.doi.org/10.1021/acsomega.1c05399
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