Binding mechanism and binding free energy of amino acids and citrate to hydroxyapatite surfaces as a function of crystallographic facet, pH, and electrolytes.


Journal

Journal of colloid and interface science
ISSN: 1095-7103
Titre abrégé: J Colloid Interface Sci
Pays: United States
ID NLM: 0043125

Informations de publication

Date de publication:
Jan 2022
Historique:
received: 27 03 2021
revised: 19 07 2021
accepted: 20 07 2021
pubmed: 9 8 2021
medline: 21 10 2021
entrez: 8 8 2021
Statut: ppublish

Résumé

Hydroxyapatite (HAP) is the major mineral phase in bone and teeth. The interaction of individual amino acids and citrate ions with different crystallographic HAP surfaces has remained uncertain for decades, creating a knowledge gap to rationally design interactions with peptides, proteins, and drugs. In this contribution, we quantify the binding mechanisms and binding free energies of the 20 end-capped natural amino acids and citrate ions on the basal (001) and prismatic (010)/(020) planes of hydroxyapatite at pH values of 7 and 5 for the first time at the molecular scale. We utilized over 1500 steered molecular dynamics simulations with highly accurate potentials that reproduce surface and hydration energies of (hkl) hydroxyapatite surfaces at different pH values. Charged residues demonstrate a much higher affinity to HAP than charge-neutral species due to the formation of superficial ion pairs and ease of penetration into layers of water molecules on the mineral surface. Binding free energies range from 0 to -60 kJ/mol and were determined with ∼ 10% uncertainty. The highest affinity was found for citrate, followed by Asp(-) and Glu(-), and followed after a gap by Arg(+), Lys(+), as well as by His(+) at pH 5. The (hkl)-specific area density of calcium ions, the protonation state of phosphate ions, and subsurface directional order of the ions in HAP lead to surface-specific binding patterns. Amino acids without ionic side groups exhibit weak binding, between -3 and 0 kJ/mol, due to difficulties to penetrate the first layer of water molecules on the apatite surfaces. We explain recognition processes that remained elusive in experiments, in prior simulations, discuss agreement with available data, and reconcile conflicting interpretations. The findings can serve as useful input for the design of peptides, proteins, and drug molecules for the modification of bone and teeth-related materials, as well as control of apatite mineralization.

Identifiants

pubmed: 34365305
pii: S0021-9797(21)01171-1
doi: 10.1016/j.jcis.2021.07.109
pii:
doi:

Substances chimiques

Amino Acids 0
Water 059QF0KO0R
Citric Acid 2968PHW8QP
Durapatite 91D9GV0Z28

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

685-700

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Samuel E Hoff (SE)

Department of Chemical and Biological Engineering, University of Colorado Boulder, Boulder, CO 80309, USA.

Juan Liu (J)

Department of Chemical and Biological Engineering, University of Colorado Boulder, Boulder, CO 80309, USA; Department of Materials Science and Engineering, Dalian Maritime University, Dalian, Liaoning 116026, China.

Hendrik Heinz (H)

Department of Chemical and Biological Engineering, University of Colorado Boulder, Boulder, CO 80309, USA. Electronic address: hendrik.heinz@colorado.edu.

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Classifications MeSH