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Duplicated or Hybridized Peptide Functional Domains Promote Oral Homeostasis.
Basiri, T; Johnson, N D; Moffa, E B; Mulyar, Y; Serra Nunes, P L; Machado, M A A M; Siqueira, W L.
Afiliação
  • Basiri T; 1 School of Dentistry and Department of Biochemistry, Schulich School of Medicine & Dentistry, The University of Western Ontario, London, ON, Canada.
  • Johnson ND; 1 School of Dentistry and Department of Biochemistry, Schulich School of Medicine & Dentistry, The University of Western Ontario, London, ON, Canada.
  • Moffa EB; 1 School of Dentistry and Department of Biochemistry, Schulich School of Medicine & Dentistry, The University of Western Ontario, London, ON, Canada.
  • Mulyar Y; 2 Department of Pediatric Dentistry, Orthodontics and Public Health, Bauru Dental School, University of São Paulo, Bauru, Brazil.
  • Serra Nunes PL; 3 CEUMA University, Post-Graduate Program in Dentistry, Maranhão, Brazil.
  • Machado MAAM; 1 School of Dentistry and Department of Biochemistry, Schulich School of Medicine & Dentistry, The University of Western Ontario, London, ON, Canada.
  • Siqueira WL; 3 CEUMA University, Post-Graduate Program in Dentistry, Maranhão, Brazil.
J Dent Res ; 96(10): 1162-1167, 2017 Sep.
Article em En | MEDLINE | ID: mdl-28511604
ABSTRACT
Proteins that have existed for millions of years frequently contain repeats of functional domains within their primary structure, thereby improving their functional capacity. In the evolutionary young statherin protein contained within the in vivo-acquired enamel pellicle (AEP), we identified a single functional domain (DR9) located within the protein N-terminal portion that exhibits a higher affinity for hydroxyapatite and more efficient protection against enamel demineralization compared to other native statherin peptides. Thus, we tested the hypothesis that multiplication of functional domains of naturally occurring pellicle peptides amplifies protection against enamel demineralization. In addition, a specific amino acid sequence from histatin 3 (RR-14) was introduced to the hybrid peptides for further testing. Enamel specimens were sectioned to 150-µm thickness and randomly grouped as follows DR9, DR9-DR9, DR9-RR14, statherin, histatin 1, or distilled water (control). After submersion for 2 h at 37°C, the specimens were placed in 2 mL demineralization solution for 12 d at 37°C. Upon sample removal, the remaining solution was subjected to colorimetric assays to determine the amount of calcium and phosphate released from each specimen. DR9-DR9 amplified protection against enamel demineralization when compared to single DR9 or statherin. Notably, the hybrid peptide DR9-RR14 demonstrated relatively strong protection when the antimicrobial property of these peptides was tested against Candida albicans and Streptococcus mutans. DR9-RR14 was able to maintain 50% of the antifungal activity compared with RR14 for C. albicans and similar values of S. mutans killing activity. This study has pioneered the functional exploration of the natural peptide constituents of the AEP and their evolution-inspired engineered peptides. The knowledge obtained here may provide a basis for the development of stable (proteinase-resistant) synthetic peptides for therapeutic use against dental caries, dental erosion, and/or oral candidiasis.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas e Peptídeos Salivares / Durapatita / Proteínas do Esmalte Dentário / Película Dentária / Homeostase Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas e Peptídeos Salivares / Durapatita / Proteínas do Esmalte Dentário / Película Dentária / Homeostase Idioma: En Ano de publicação: 2017 Tipo de documento: Article