{Reference Type}: Journal Article
{Title}: Self-assembled peptide P11-4 interacts with the type I collagen C-terminal telopeptide domain and calcium ions.
{Author}: Carvalho RG;Patekoski LF;Puppin-Rontani RM;Nakaie CR;Nascimento FD;Tersariol ILS;
{Journal}: Dent Mater
{Volume}: 39
{Issue}: 8
{Year}: 2023 08 30
{Factor}: 5.687
{DOI}: 10.1016/j.dental.2023.06.004
{Abstract}: Evaluate molecularly the role of P11-4 self-assembly peptide in dentin remineralization and its interaction with collagen I.<BR>The calcium-responsive P11-4 peptide was analyzed by intrinsic fluorescence emission spectrum, circular dichroism spectrum (CD), and atomic force microscope (AFM). Differential light scattering was used to monitor the nucleation growth rate of calcium phosphate nanocrystals in the absence or in the presence of P11-4. AFM was used to analyze the radial size (nm) of calcium phosphate nanocrystals formed in the absence or in the presence of P11-4, as well as to verify the spatial structure of P11-4 in the absence or in the presence of Ca2+.<BR>The interaction of Ca2+ with the P11-4 (KD = 0.58 ± 0.06 mM) promotes the formation of β-sheet antiparallel structure, leads to its precipitation in saturated solutions of Ca/P = 1.67 and induces the formation of parallel large fibrils (0.6 - 1.5 µm). P11-4 organized the HAP nucleation by reducing both the growth rate and size variability of nanocrystals, analyzed by the F test (p < 0.0001, N = 30). P11-4 interacts (KD = 0.75 ± 0.06 μM) with the KGHRGFSGL motif present at the C-terminal collagen telopeptide domain. P11-4 also increased the amount of HAP and collagen in the MDPC-23 cells.<BR>The presented data propose a mechanism that will help future clinical and/or basic research to better understand a molecule able to inhibit structural collagen loss and help the impaired tissue to remineralize.