Literature DB >> 28511604

Duplicated or Hybridized Peptide Functional Domains Promote Oral Homeostasis.

T Basiri1, N D Johnson1, E B Moffa1,2,3, Y Mulyar1, P L Serra Nunes3, M A A M Machado2, W L Siqueira1.   

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.

Entities:  

Keywords:  demineralization; dental caries; enamel pellicle; oral health; saliva; salivary proteins

Mesh:

Substances:

Year:  2017        PMID: 28511604     DOI: 10.1177/0022034517708552

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  5 in total

1.  Efficacy of the dual-action GA-KR12 peptide for remineralising initial enamel caries: an in vitro study.

Authors:  John Yun Niu; Iris Xiaoxue Yin; William Ka Kei Wu; Quan-Li Li; May Lei Mei; Chun Hung Chu
Journal:  Clin Oral Investig       Date:  2021-10-12       Impact factor: 3.573

2.  Acquired Enamel Pellicle Engineered Peptides: Effects on Hydroxyapatite Crystal Growth.

Authors:  Maria Teresa Valente; Eduardo Buozi Moffa; Karla Tonelli Bicalho Crosara; Yizhi Xiao; Thais Marchini de Oliveira; Maria Aparecida de Andrade Moreira Machado; Walter Luiz Siqueira
Journal:  Sci Rep       Date:  2018-02-28       Impact factor: 4.379

3.  pH-Sensitive Chitosan Nanoparticles for Salivary Protein Delivery.

Authors:  Yi Zhu; Lina M Marin; Yizhi Xiao; Elizabeth R Gillies; Walter L Siqueira
Journal:  Nanomaterials (Basel)       Date:  2021-04-17       Impact factor: 5.076

4.  Modulation of Streptococcus mutans Adherence to Hydroxyapatite by Engineered Salivary Peptides.

Authors:  Lina Maria Marin; Yizhi Xiao; Jaime Aparecido Cury; Walter Luiz Siqueira
Journal:  Microorganisms       Date:  2022-01-20

5.  Engineered Salivary Peptides Reduce Enamel Demineralization Provoked by Cariogenic S. mutans Biofilm.

Authors:  Lina Maria Marin; Yizhi Xiao; Jaime Aparecido Cury; Walter Luiz Siqueira
Journal:  Microorganisms       Date:  2022-03-30
  5 in total

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