Quantifying the efficiency of Hydroxyapatite Mineralising Peptides

Abstract We present a non-destructive analytical calibration tool to allow quantitative assessment of individual calcium phosphates such as hydroxyapatite (HAP) from mixtures including brushite. Many experimental approaches are used to evaluate the mineralising capabilities of biomolecules including...

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Main Authors: Robyn Plowright, David J. Belton, David L. Kaplan, Carole C. Perry
Format: Article
Language:English
Published: Nature Portfolio 2017-08-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-07247-z
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author Robyn Plowright
David J. Belton
David L. Kaplan
Carole C. Perry
author_facet Robyn Plowright
David J. Belton
David L. Kaplan
Carole C. Perry
author_sort Robyn Plowright
collection DOAJ
description Abstract We present a non-destructive analytical calibration tool to allow quantitative assessment of individual calcium phosphates such as hydroxyapatite (HAP) from mixtures including brushite. Many experimental approaches are used to evaluate the mineralising capabilities of biomolecules including peptides. However, it is difficult to quantitatively compare the efficacy of peptides in the promotion of mineralisation when inseparable mixtures of different minerals are produced. To address this challenge, a series of hydroxyapatite and brushite mixtures were produced as a percent/weight (0–100%) from pure components and multiple (N = 10) XRD patterns were collected for each mixture. A linear relationship between the ratio of selected peak heights and the molar ratio was found. Using this method, the mineralising capabilities of three known hydroxyapatite binding peptides, CaP(S) STLPIPHEFSRE, CaP(V) VTKHLNQISQSY and CaP(H) SVSVGMKPSPRP, was compared. All three directed mineralisation towards hydroxyapatite in a peptide concentration dependent manner. CaP(V) was most effective at inducing hydroxyapatite formation at higher reagent levels (Ca2+ = 200 mM), as also seen with peptide-silk chimeric materials, whereas CaP(S) was most effective when lower concentrations of calcium (20 mM) and phosphate were used. The approach can be extended to investigate HAP mineralisation in the presence of any number of mineralisation promoters or inhibitors.
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spelling doaj.art-17e3fc5403d54507a659756aed5305ec2022-12-21T19:08:33ZengNature PortfolioScientific Reports2045-23222017-08-01711910.1038/s41598-017-07247-zQuantifying the efficiency of Hydroxyapatite Mineralising PeptidesRobyn Plowright0David J. Belton1David L. Kaplan2Carole C. Perry3Biomolecular and Materials Interface Research Group, Interdisciplinary Biomedical Research Centre, School of Science and Technology, Nottingham Trent University, Clifton LaneBiomolecular and Materials Interface Research Group, Interdisciplinary Biomedical Research Centre, School of Science and Technology, Nottingham Trent University, Clifton LaneDepartment of Biomedical Engineering, Tufts UniversityBiomolecular and Materials Interface Research Group, Interdisciplinary Biomedical Research Centre, School of Science and Technology, Nottingham Trent University, Clifton LaneAbstract We present a non-destructive analytical calibration tool to allow quantitative assessment of individual calcium phosphates such as hydroxyapatite (HAP) from mixtures including brushite. Many experimental approaches are used to evaluate the mineralising capabilities of biomolecules including peptides. However, it is difficult to quantitatively compare the efficacy of peptides in the promotion of mineralisation when inseparable mixtures of different minerals are produced. To address this challenge, a series of hydroxyapatite and brushite mixtures were produced as a percent/weight (0–100%) from pure components and multiple (N = 10) XRD patterns were collected for each mixture. A linear relationship between the ratio of selected peak heights and the molar ratio was found. Using this method, the mineralising capabilities of three known hydroxyapatite binding peptides, CaP(S) STLPIPHEFSRE, CaP(V) VTKHLNQISQSY and CaP(H) SVSVGMKPSPRP, was compared. All three directed mineralisation towards hydroxyapatite in a peptide concentration dependent manner. CaP(V) was most effective at inducing hydroxyapatite formation at higher reagent levels (Ca2+ = 200 mM), as also seen with peptide-silk chimeric materials, whereas CaP(S) was most effective when lower concentrations of calcium (20 mM) and phosphate were used. The approach can be extended to investigate HAP mineralisation in the presence of any number of mineralisation promoters or inhibitors.https://doi.org/10.1038/s41598-017-07247-z
spellingShingle Robyn Plowright
David J. Belton
David L. Kaplan
Carole C. Perry
Quantifying the efficiency of Hydroxyapatite Mineralising Peptides
Scientific Reports
title Quantifying the efficiency of Hydroxyapatite Mineralising Peptides
title_full Quantifying the efficiency of Hydroxyapatite Mineralising Peptides
title_fullStr Quantifying the efficiency of Hydroxyapatite Mineralising Peptides
title_full_unstemmed Quantifying the efficiency of Hydroxyapatite Mineralising Peptides
title_short Quantifying the efficiency of Hydroxyapatite Mineralising Peptides
title_sort quantifying the efficiency of hydroxyapatite mineralising peptides
url https://doi.org/10.1038/s41598-017-07247-z
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