Investigation of multiwall carbon nanotube modified hydroxyapatite on human osteoblast cell line using iTRAQ proteomics technology

Hydroxyapatite (HA) is a bioactive ceramic material with a chemical composition similar to natural bone, and carbon nano tubes (CNT) is able to enhance the brittle ceramic matrix without detrimental to the bioactivity. This study reported an attempt to use a commercially multiwalled CNT strengthen b...

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Main Authors: Xu, J. L., Khor, K. A., Sui, J. J., Chen, William Wei Ning
Other Authors: School of Chemical and Biomedical Engineering
Format: Article
Language:English
Published: 2014
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Online Access:https://hdl.handle.net/10356/101953
http://hdl.handle.net/10220/18811
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1019532023-03-04T17:20:00Z Investigation of multiwall carbon nanotube modified hydroxyapatite on human osteoblast cell line using iTRAQ proteomics technology Xu, J. L. Khor, K. A. Sui, J. J. Chen, William Wei Ning School of Chemical and Biomedical Engineering School of Mechanical and Aerospace Engineering DRNTU::Engineering::Materials Hydroxyapatite (HA) is a bioactive ceramic material with a chemical composition similar to natural bone, and carbon nano tubes (CNT) is able to enhance the brittle ceramic matrix without detrimental to the bioactivity. This study reported an attempt to use a commercially multiwalled CNT strengthen brittle hydroxyapatite bioceramics. Using iTRAQ-coupled 2D LCMS/ MS analysis, we report the first study of protein profile in osteoblasts from human osteoblastic cell line incubated separately on HA with and without strengthening multiwall CNT surfaces. Sixty proteins were identified and quantified simultaneously at the initial culturing stage of 3 days. The results were validated by Western blotting for selected proteins: Fetuin-A, Elongation factor II and Peroxiredoxin VI. Fetuin-A showed up-regulation, and Peroxiredoxin VI gave down-regulation in the osteoblasts cultured on HA based ceramic surfaces. Similar regulation was expressed by the protein of Elongation factor II on the phase pure HA surfaces as compared to the control group cultured on the polystyrene substrate. Relatively high EF 2 expression was detected on the phase the surfaces of CNT strengthen HA samples. Accepted version 2014-02-17T09:16:38Z 2019-12-06T20:47:17Z 2014-02-17T09:16:38Z 2019-12-06T20:47:17Z 2008 2008 Journal Article Xu, J. L., Khor, K. A., Sui, J. J., & Chen, W. N. (2008). Investigation of multiwall carbon nanotube modified hydroxyapatite on human osteoblast cell line using iTRAQ proteomics technology. Key engineering materials, 361-363, 1047-1050. 1662-9795 https://hdl.handle.net/10356/101953 http://hdl.handle.net/10220/18811 10.4028/www.scientific.net/KEM.361-363.1047 en Key engineering materials © 2008 Trans Tech Publications.This is the author created version of a work that has been peer reviewed and accepted for publication by Key Engineering Materials, Trans Tech Publications. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.4028/www.scientific.net/KEM.361-363.1047]. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Engineering::Materials
spellingShingle DRNTU::Engineering::Materials
Xu, J. L.
Khor, K. A.
Sui, J. J.
Chen, William Wei Ning
Investigation of multiwall carbon nanotube modified hydroxyapatite on human osteoblast cell line using iTRAQ proteomics technology
description Hydroxyapatite (HA) is a bioactive ceramic material with a chemical composition similar to natural bone, and carbon nano tubes (CNT) is able to enhance the brittle ceramic matrix without detrimental to the bioactivity. This study reported an attempt to use a commercially multiwalled CNT strengthen brittle hydroxyapatite bioceramics. Using iTRAQ-coupled 2D LCMS/ MS analysis, we report the first study of protein profile in osteoblasts from human osteoblastic cell line incubated separately on HA with and without strengthening multiwall CNT surfaces. Sixty proteins were identified and quantified simultaneously at the initial culturing stage of 3 days. The results were validated by Western blotting for selected proteins: Fetuin-A, Elongation factor II and Peroxiredoxin VI. Fetuin-A showed up-regulation, and Peroxiredoxin VI gave down-regulation in the osteoblasts cultured on HA based ceramic surfaces. Similar regulation was expressed by the protein of Elongation factor II on the phase pure HA surfaces as compared to the control group cultured on the polystyrene substrate. Relatively high EF 2 expression was detected on the phase the surfaces of CNT strengthen HA samples.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Xu, J. L.
Khor, K. A.
Sui, J. J.
Chen, William Wei Ning
format Article
author Xu, J. L.
Khor, K. A.
Sui, J. J.
Chen, William Wei Ning
author_sort Xu, J. L.
title Investigation of multiwall carbon nanotube modified hydroxyapatite on human osteoblast cell line using iTRAQ proteomics technology
title_short Investigation of multiwall carbon nanotube modified hydroxyapatite on human osteoblast cell line using iTRAQ proteomics technology
title_full Investigation of multiwall carbon nanotube modified hydroxyapatite on human osteoblast cell line using iTRAQ proteomics technology
title_fullStr Investigation of multiwall carbon nanotube modified hydroxyapatite on human osteoblast cell line using iTRAQ proteomics technology
title_full_unstemmed Investigation of multiwall carbon nanotube modified hydroxyapatite on human osteoblast cell line using iTRAQ proteomics technology
title_sort investigation of multiwall carbon nanotube modified hydroxyapatite on human osteoblast cell line using itraq proteomics technology
publishDate 2014
url https://hdl.handle.net/10356/101953
http://hdl.handle.net/10220/18811
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