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Synthesis of a Potentially Bioactive, Hydroxyapatite-Nucleating Molecule

Calcified Tissue International volume 78, pages 55–61 (2006)Cite this article

Abstract

A human phosphophoryn (PP) cDNA was previously cloned from immature root apex total RNA in our laboratory. This cDNA comprises 2,364 bp, encoding 788 amino acids. More than 80% of the sequences are arranged as (DSS) n (n = 1–16), DS, and NSS motifs. We hypothesize that the capability of PP to bind Ca2+ and nucleate hydroxyapatite may depend on these repeated sequences. Two polypeptides were synthesized based on the human PP cDNA sequence to test the hypothesis. One polypeptide has the amino acid sequence DDPNSSDESNGNDD (synthetic polypeptide 1, SP1), which is from the N-terminal end of PP; the other polypeptide, DSKSDSSKSESDSS (synthetic polypeptide 2, SP2), is the PP repeated sequence motif. Phosphorylation of the polypeptides was accomplished by reacting them with adenosine triphosphate and casein kinases I and II. The ability of these molecules to cause mineralization was tested in a steady-state agarose gel system. The results show that phosphorylated SP2 (P-SP2) precipitated approximately 60% of the total Ca + PO4 precipitated by PP. P-SP1 precipitated about 23% of that precipitated by PP and was similar to the amount precipitated in the control gel, that is, without added peptides. Transmission electron microscopy and X-ray diffraction analysis showed that the precipitate formed in the P-SP2-containing gel was hydroxyapatite. The capability of P-SP2 to nucleate Ca + PO4 and precipitate hydroxyapatite is a result of the repeated sequence motif, which contains a high percentage of phosphorylated serine. This molecule could be used in the repair and regeneration of dental tissue.

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Acknowledgments

We thank Dr. Kai Sun and Dr. John F. Mansfield for their help with the TEM analysis. We also thank Dr. Qiming Jin for his help in improving the TEM image. This investigation was supported by NIH grant DE 12899.

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Affiliations

  1. Department of Cariology, Restorative Sciences, and Endodontics, University of Michigan, Ann Arbor, MI, USA

    S. Chang, H. Chen, J. Liu & B. Clarkson

  2. Division of Restorative Dentistry, University of Leeds, Leeds, United Kingdom

    D. Wood & P. Bentley

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  1. S. Chang
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  2. H. Chen
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  3. J. Liu
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Correspondence to S. Chang.

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Chang, S., Chen, H., Liu, J. et al. Synthesis of a Potentially Bioactive, Hydroxyapatite-Nucleating Molecule. Calcif Tissue Int 78, 55–61 (2006). https://doi.org/10.1007/s00223-005-0118-4

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  • DOI: https://doi.org/10.1007/s00223-005-0118-4

Keywords

  • Human
  • Phosphophoryn
  • Polypeptide
  • Hydroxyapatite
  • Nucleation