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Promoting effect of a calcium-responsive self-assembly β-sheet peptide on collagen intrafibrillar mineralization

Recently, a de novo synthetic calcium-responsive self-assembly β-sheet peptide ID8 (Ile-Asp-Ile-Asp-Ile-Asp-Ile-Asp) has been developed to serve as the template inducing hydroxyapatite nucleation. The aim of this study was to evaluate the effect of ID8 on intrafibrillar mineralization of collagen ma...

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Autores principales: Li, Zhongcheng, Ren, Qian, Han, Sili, Ding, Longjiang, Qin, Xi, Hu, Die, He, Ting, Tian, Tian, Lu, Ziqian, Zhang, Linglin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9514854/
https://www.ncbi.nlm.nih.gov/pubmed/36176712
http://dx.doi.org/10.1093/rb/rbac059
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author Li, Zhongcheng
Ren, Qian
Han, Sili
Ding, Longjiang
Qin, Xi
Hu, Die
He, Ting
Tian, Tian
Lu, Ziqian
Zhang, Linglin
author_facet Li, Zhongcheng
Ren, Qian
Han, Sili
Ding, Longjiang
Qin, Xi
Hu, Die
He, Ting
Tian, Tian
Lu, Ziqian
Zhang, Linglin
author_sort Li, Zhongcheng
collection PubMed
description Recently, a de novo synthetic calcium-responsive self-assembly β-sheet peptide ID8 (Ile-Asp-Ile-Asp-Ile-Asp-Ile-Asp) has been developed to serve as the template inducing hydroxyapatite nucleation. The aim of this study was to evaluate the effect of ID8 on intrafibrillar mineralization of collagen making full use of its self-assembly ability. The mineralization experiments were carried out in vitro on both bare Type I collagen and fully demineralized dentin samples. The calcium-responsive self-assembly of ID8 was revealed by circular dichroism spectrum, 8-anilino-1-naphthalenesulfonic acid ammonium salt hydrate assay, attenuated total reflection Fourier transform infrared spectrum (ATR-FTIR) and transmission electron microscope (TEM). Polyacrylic acid (450 kDa) with a concentration of 100 μg ml(−1) was selected as the nucleation inhibitor based on the determination of turbidimetry and TEM with selected area electron diffraction (TEM-SAED). The results showed that collagen intrafibrillar mineralization was significantly promoted with the pretreatment of self-assembly ID8 detected by TEM-SAED, SEM, X-ray diffraction and ATR-FTIR. The pretreatment of collagen utilizing self-assembly ID8 not only enhanced intermolecular hydrogen bonding but also contributed to calcium retention inside collagen and significantly increased the hydrophilicity of collagen. These results indicated that peptides with self-assembly properties like ID8 are expected to be potential tools for biomimetic mineralization of collagen.
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spelling pubmed-95148542022-09-28 Promoting effect of a calcium-responsive self-assembly β-sheet peptide on collagen intrafibrillar mineralization Li, Zhongcheng Ren, Qian Han, Sili Ding, Longjiang Qin, Xi Hu, Die He, Ting Tian, Tian Lu, Ziqian Zhang, Linglin Regen Biomater Research Article Recently, a de novo synthetic calcium-responsive self-assembly β-sheet peptide ID8 (Ile-Asp-Ile-Asp-Ile-Asp-Ile-Asp) has been developed to serve as the template inducing hydroxyapatite nucleation. The aim of this study was to evaluate the effect of ID8 on intrafibrillar mineralization of collagen making full use of its self-assembly ability. The mineralization experiments were carried out in vitro on both bare Type I collagen and fully demineralized dentin samples. The calcium-responsive self-assembly of ID8 was revealed by circular dichroism spectrum, 8-anilino-1-naphthalenesulfonic acid ammonium salt hydrate assay, attenuated total reflection Fourier transform infrared spectrum (ATR-FTIR) and transmission electron microscope (TEM). Polyacrylic acid (450 kDa) with a concentration of 100 μg ml(−1) was selected as the nucleation inhibitor based on the determination of turbidimetry and TEM with selected area electron diffraction (TEM-SAED). The results showed that collagen intrafibrillar mineralization was significantly promoted with the pretreatment of self-assembly ID8 detected by TEM-SAED, SEM, X-ray diffraction and ATR-FTIR. The pretreatment of collagen utilizing self-assembly ID8 not only enhanced intermolecular hydrogen bonding but also contributed to calcium retention inside collagen and significantly increased the hydrophilicity of collagen. These results indicated that peptides with self-assembly properties like ID8 are expected to be potential tools for biomimetic mineralization of collagen. Oxford University Press 2022-09-05 /pmc/articles/PMC9514854/ /pubmed/36176712 http://dx.doi.org/10.1093/rb/rbac059 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Zhongcheng
Ren, Qian
Han, Sili
Ding, Longjiang
Qin, Xi
Hu, Die
He, Ting
Tian, Tian
Lu, Ziqian
Zhang, Linglin
Promoting effect of a calcium-responsive self-assembly β-sheet peptide on collagen intrafibrillar mineralization
title Promoting effect of a calcium-responsive self-assembly β-sheet peptide on collagen intrafibrillar mineralization
title_full Promoting effect of a calcium-responsive self-assembly β-sheet peptide on collagen intrafibrillar mineralization
title_fullStr Promoting effect of a calcium-responsive self-assembly β-sheet peptide on collagen intrafibrillar mineralization
title_full_unstemmed Promoting effect of a calcium-responsive self-assembly β-sheet peptide on collagen intrafibrillar mineralization
title_short Promoting effect of a calcium-responsive self-assembly β-sheet peptide on collagen intrafibrillar mineralization
title_sort promoting effect of a calcium-responsive self-assembly β-sheet peptide on collagen intrafibrillar mineralization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9514854/
https://www.ncbi.nlm.nih.gov/pubmed/36176712
http://dx.doi.org/10.1093/rb/rbac059
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