Almora-Barrios, N; de Leeuw, NH; (2010) A Density Functional Theory Study of the Interaction of Collagen Peptides with Hydroxyapatite Surfaces. LANGMUIR , 26 (18) 14535 - 14542. 10.1021/la101151e.
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Density functional theory calculations were applied to investigate the binding of four peptide strands, which are important in the collagen protein, to the bone and tooth mineral hydroxyapatite amphiphilic PRO-HYP-GLY and HYP-PRO-GLY. and hydrphobic PRO-LYS-GLY and PRO-HYL-GLY The particular peptide sequences are chosen for their different functional groups, containing (i) hydrophobic, (n) uncharged polar; and (iii) charged polar side groups, thus allowing direct comparison of the general effect of these carboxylic acid and amine functional groups, as well as hydroxylation and charge. on then interactions with two major hydroxyapatite surfaces. (0001) and (0110) The calculated results in e consistent with experiments. confirming that the terminal carboxyl groups and amine groups mainly contribute to the adsorption of the peptides to the hydroxyapatite surfaces and primarily to the (0110) sin face rather than the dominant (0001) plane Of the side groups in the tripeptide motifs representing the collagen protein, the OH and positively charged -NH3+ groups in particular bind strongly to the surfaces, and their presence should therefore promote hydioxyapatite growth.
|Title:||A Density Functional Theory Study of the Interaction of Collagen Peptides with Hydroxyapatite Surfaces|
|Keywords:||SOLID-STATE NMR, MOLECULAR-DYNAMICS SIMULATIONS, NANOSCALE MECHANICAL-BEHAVIOR, POLAR SIDE-GROUPS, AMINO-ACIDS, 01(1)OVER-BAR0 SURFACES, HARD BIOMATERIALS, CITRIC-ACID, ADSORPTION, STATHERIN|
|UCL classification:||UCL > School of BEAMS > Faculty of Maths and Physical Sciences > Chemistry|
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