Multifaceted Influences of Melanin-Like Particles on Amyloid-beta Aggregation
- Authors
- Song, Haeun; Kim, Yoonyoung; Kim, Inkyu; Kim, Young-Kwan; Kwon, Sunbum; Kang, Kyungtae
- Issue Date
- 2-Jan-2020
- Publisher
- WILEY-V C H VERLAG GMBH
- Keywords
- amyloid beta-peptides; amyloids; bioorganic chemistry; melanin-like particles; polydopamine
- Citation
- CHEMISTRY-AN ASIAN JOURNAL, v.15, no.1, pp 91 - 97
- Pages
- 7
- Indexed
- SCIE
SCOPUS
- Journal Title
- CHEMISTRY-AN ASIAN JOURNAL
- Volume
- 15
- Number
- 1
- Start Page
- 91
- End Page
- 97
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/7007
- DOI
- 10.1002/asia.201901405
- ISSN
- 1861-4728
1861-471X
- Abstract
- The properties of eumelanin-like particles (EMPs) and pheomelanin-like particles (PMPs) in regulating the process of amyloid formation of amyloid-beta 42 (A beta 42) were examined. EMPs and PMPs are effective both in interfering with amyloid aggregation of A beta 42 and in remodeling matured Alpha beta 42 fibers. The results suggest that some (but not all) molecular species consisting of melanin-like particles (MPs) are responsible for their inhibiting property toward amyloid formation, and the influence is likely manifested by long-range interactions. Incubating preformed A beta 42 fibers with catechols or MPs leads to the formation of mesh-like, interconnected A beta 42 fibers encapsulated with melanin-like material. MPs are kinetically more effective than catechol monomers in this process, and a detailed investigation reveals that 4,5-dihydroxyindole, a major intermediate in the formation of melanin-like species, and its derivatives are mainly responsible for remodeling amyloid fibers.
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- Appears in
Collections - College of Natural Science > Department of Chemistry > 1. Journal Articles

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