TY - JOUR
T1 - Uniaxial hydroxyapatite growth on a self‐assembled protein scaffold
AU - Danesi, Alexander L.
AU - Athanasiadou, Dimitra
AU - Mansouri, Ahmad
AU - Phen, Alina
AU - Neshatian, Mehrnoosh
AU - Holcroft, James
AU - Bonde, Johan
AU - Ganss, Bernhard
AU - Carneiro, Karina M.M.
N1 - Funding Information:
Funding: This work was supported by grants from the Natural Sciences and Engineering Research Council of Canada (NSERC; RGPIN‐2017‐06885 to K.M.M.C. and RGPIN‐2019‐07070 to B.G.). Ad‐ ditional support was received from the Bertha Rosenstadt Endowment Fund. The authors declare no potential conflicts of interest with respect to the authorship and/or publication of this article.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/11/1
Y1 - 2021/11/1
N2 - 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, ame-logenin 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.
AB - 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, ame-logenin 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.
KW - Amelogenin
KW - Amelotin hydroxyapatite
KW - Biomimetics
KW - Biomineralization
KW - Bio‐inspired materials
KW - Enamel
U2 - 10.3390/ijms222212343
DO - 10.3390/ijms222212343
M3 - Article
C2 - 34830225
AN - SCOPUS:85118953582
SN - 1661-6596
VL - 22
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 22
M1 - 12343
ER -