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Contribution of biomimetic collagen-ligand interaction to intrafibrillar mineralization

Contemporary models of intrafibrillar mineralization mechanisms are established using collagen fibrils as templates without considering the contribution from collagen-bound apatite nucleation inhibitors. However, collagen matrices destined for mineralization in vertebrates contain bound matrix prote...

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Autores principales: Song, Q., Jiao, K., Tonggu, L., Wang, L. G., Zhang, S. L., Yang, Y. D., Zhang, L., Bian, J. H., Hao, D. X., Wang, C. Y., Ma, Y. X., Arola, D. D., Breschi, L., Chen, J. H., Tay, F. R., Niu, L. N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459768/
https://www.ncbi.nlm.nih.gov/pubmed/30989106
http://dx.doi.org/10.1126/sciadv.aav9075
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author Song, Q.
Jiao, K.
Tonggu, L.
Wang, L. G.
Zhang, S. L.
Yang, Y. D.
Zhang, L.
Bian, J. H.
Hao, D. X.
Wang, C. Y.
Ma, Y. X.
Arola, D. D.
Breschi, L.
Chen, J. H.
Tay, F. R.
Niu, L. N.
author_facet Song, Q.
Jiao, K.
Tonggu, L.
Wang, L. G.
Zhang, S. L.
Yang, Y. D.
Zhang, L.
Bian, J. H.
Hao, D. X.
Wang, C. Y.
Ma, Y. X.
Arola, D. D.
Breschi, L.
Chen, J. H.
Tay, F. R.
Niu, L. N.
author_sort Song, Q.
collection PubMed
description Contemporary models of intrafibrillar mineralization mechanisms are established using collagen fibrils as templates without considering the contribution from collagen-bound apatite nucleation inhibitors. However, collagen matrices destined for mineralization in vertebrates contain bound matrix proteins for intrafibrillar mineralization. Negatively charged, high–molecular weight polycarboxylic acid is cross-linked to reconstituted collagen to create a model for examining the contribution of collagen-ligand interaction to intrafibrillar mineralization. Cryogenic electron microscopy and molecular dynamics simulation show that, after cross-linking to collagen, the bound polyelectrolyte caches prenucleation cluster singlets into chain-like aggregates along the fibrillar surface to increase the pool of mineralization precursors available for intrafibrillar mineralization. Higher-quality mineralized scaffolds with better biomechanical properties are achieved compared with mineralization of unmodified scaffolds in polyelectrolyte-stabilized mineralization solution. Collagen-ligand interaction provides insights on the genesis of heterogeneously mineralized tissues and the potential causes of ectopic calcification in nonmineralized body tissues.
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spelling pubmed-64597682019-04-15 Contribution of biomimetic collagen-ligand interaction to intrafibrillar mineralization Song, Q. Jiao, K. Tonggu, L. Wang, L. G. Zhang, S. L. Yang, Y. D. Zhang, L. Bian, J. H. Hao, D. X. Wang, C. Y. Ma, Y. X. Arola, D. D. Breschi, L. Chen, J. H. Tay, F. R. Niu, L. N. Sci Adv Research Articles Contemporary models of intrafibrillar mineralization mechanisms are established using collagen fibrils as templates without considering the contribution from collagen-bound apatite nucleation inhibitors. However, collagen matrices destined for mineralization in vertebrates contain bound matrix proteins for intrafibrillar mineralization. Negatively charged, high–molecular weight polycarboxylic acid is cross-linked to reconstituted collagen to create a model for examining the contribution of collagen-ligand interaction to intrafibrillar mineralization. Cryogenic electron microscopy and molecular dynamics simulation show that, after cross-linking to collagen, the bound polyelectrolyte caches prenucleation cluster singlets into chain-like aggregates along the fibrillar surface to increase the pool of mineralization precursors available for intrafibrillar mineralization. Higher-quality mineralized scaffolds with better biomechanical properties are achieved compared with mineralization of unmodified scaffolds in polyelectrolyte-stabilized mineralization solution. Collagen-ligand interaction provides insights on the genesis of heterogeneously mineralized tissues and the potential causes of ectopic calcification in nonmineralized body tissues. American Association for the Advancement of Science 2019-03-29 /pmc/articles/PMC6459768/ /pubmed/30989106 http://dx.doi.org/10.1126/sciadv.aav9075 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Song, Q.
Jiao, K.
Tonggu, L.
Wang, L. G.
Zhang, S. L.
Yang, Y. D.
Zhang, L.
Bian, J. H.
Hao, D. X.
Wang, C. Y.
Ma, Y. X.
Arola, D. D.
Breschi, L.
Chen, J. H.
Tay, F. R.
Niu, L. N.
Contribution of biomimetic collagen-ligand interaction to intrafibrillar mineralization
title Contribution of biomimetic collagen-ligand interaction to intrafibrillar mineralization
title_full Contribution of biomimetic collagen-ligand interaction to intrafibrillar mineralization
title_fullStr Contribution of biomimetic collagen-ligand interaction to intrafibrillar mineralization
title_full_unstemmed Contribution of biomimetic collagen-ligand interaction to intrafibrillar mineralization
title_short Contribution of biomimetic collagen-ligand interaction to intrafibrillar mineralization
title_sort contribution of biomimetic collagen-ligand interaction to intrafibrillar mineralization
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459768/
https://www.ncbi.nlm.nih.gov/pubmed/30989106
http://dx.doi.org/10.1126/sciadv.aav9075
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