Oriented immobilization of proteins on hydroxyapatite surface using bifunctional bisphosphonates as linkers

Jivan N. Yewle, Yinan Wei, David A. Puleo, Sylvia Daunert, Leonidas G Bachas

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

Oriented immobilization of proteins is an important step in creating protein-based functional materials. In this study, a method was developed to orient proteins on hydroxyapatite (HA) surfaces, a widely used bone implant material, to improve protein bioactivity by employing enhanced green fluorescent protein (EGFP) and β-lactamase as model proteins. These proteins have a serine or threonine at their N-terminus that was oxidized with periodate to obtain a single aldehyde group at the same location, which can be used for the site-specific immobilization of the protein. The HA surface was modified with bifunctional hydrazine bisphosphonates (HBPs) of various length and lipophilicity. The number of functional groups on the HBP-modified HA surface, determined by a 2,4,6-trinitrobenzenesulfonic acid (TNBS) assay, was found to be 2.8 × 10-5 mol/mg of HA and unaffected by the length of HBPs. The oxidized proteins were immobilized on the HBP-modified HA surface in an oriented manner through formation of a hydrazone bond. The relative protein immobilization amounts through various HBPs were determined by fluorescence and bicinchoninic acid (BCA) assay and showed no significant effect by length and lipophilicity of HBPs. The relative amount of HBP-immobilized EGFP was found to be 10-15 fold that of adsorbed EGFP, whereas the relative amount of β-lactamase immobilized through HBPs (2, 3, 4, 6, and 7) was not significantly different than adsorbed β-lactamase. The enzymatic activity of HBP-immobilized β-lactamase was measured with cefazolin as substrate, and it was found that the catalytic efficiency of HBP-immobilized β-lactamase improved 2-5 fold over adsorbed β-lactamase. The results obtained demonstrate the feasibility of our oriented immobilization approach and showed an increased activity of the oriented proteins in comparison with adsorbed proteins on the same hydroxyapatite surface matrix.

Original languageEnglish
Pages (from-to)1742-1749
Number of pages8
JournalBiomacromolecules
Volume13
Issue number6
DOIs
StatePublished - Jun 11 2012

Fingerprint

hydrazine
Diphosphonates
Durapatite
Hydroxyapatite
Hydrazine
Proteins
Assays
Trinitrobenzenesulfonic Acid
Cefazolin
Hydrazones
Functional materials

ASJC Scopus subject areas

  • Bioengineering
  • Materials Chemistry
  • Polymers and Plastics
  • Biomaterials

Cite this

Oriented immobilization of proteins on hydroxyapatite surface using bifunctional bisphosphonates as linkers. / Yewle, Jivan N.; Wei, Yinan; Puleo, David A.; Daunert, Sylvia; Bachas, Leonidas G.

In: Biomacromolecules, Vol. 13, No. 6, 11.06.2012, p. 1742-1749.

Research output: Contribution to journalArticle

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