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  3. Uniaxial Hydroxyapatite Growth on a Self-Assembled Protein Scaffold
 

Uniaxial Hydroxyapatite Growth on a Self-Assembled Protein Scaffold

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BORIS DOI
10.48620/77203
Publisher DOI
10.3390/ijms222212343
PubMed ID
34830225
Description
Biomineralization is a crucial process whereby organisms produce mineralized tissues such as teeth for mastication, bones for support, and shells for protection. Mineralized tissues are composed of hierarchically organized hydroxyapatite crystals, with a limited capacity to regenerate when demineralized or damaged past a critical size. Thus, the development of protein-based materials that act as artificial scaffolds to guide hydroxyapatite growth is an attractive goal both for the design of ordered nanomaterials and for tissue regeneration. In particular, amelogenin, which is the main protein that scaffolds the hierarchical organization of hydroxyapatite crystals in enamel, amelogenin recombinamers, and amelogenin-derived peptide scaffolds have all been investigated for in vitro mineral growth. Here, we describe uniaxial hydroxyapatite growth on a nanoengineered amelogenin scaffold in combination with amelotin, a mineral promoting protein present during enamel formation. This bio-inspired approach for hydroxyapatite growth may inform the molecular mechanism of hydroxyapatite formation in vitro as well as possible mechanisms at play during mineralized tissue formation.
Date of Publication
2021-11-15
Publication Type
Article
Keyword(s)
amelogenin
•
amelotin hydroxyapatite
•
bio-inspired materials
•
biomimetics
•
biomineralization
•
enamel
Language(s)
en
Contributor(s)
Danesi, Alexander L.
Athanasiadou, Dimitra
Institute of Geological Sciences
Mansouri, Ahmad
Phen, Alina
Neshatian, Mehrnoosh
Holcroft, James
Bonde, Johan
Ganss, Bernhard
Carneiro, Karina M. M.
Additional Credits
Institute of Geological Sciences
Series
International Journal of Molecular Sciences
Publisher
MDPI
ISSN
1422-0067
1661-6596
Access(Rights)
open.access
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