The objective of this research was to determine the factors
that
influence the ability of calcium-binding peptides, obtained through
in silico enzymatic hydrolysis of whey proteins, to promote calcium
absorption. Isothermal titration calorimetry and density functional
theory calculations revealed that all of the investigated peptides
could spontaneously bind calcium through an entropy-driven endothermic
binding reaction via their terminal and side-chain carboxyl groups
at physiological pH. Among the investigated peptides, tripeptide EAC
demonstrated the strongest ability to promote calcium absorption,
with a calcium ion activity-based binding constant of 209 L/mol and
a promotion factor of 2.57. The ability of calcium-binding peptides
to promote calcium absorption was not correlated with their calcium-binding
constants but rather with their chemical hardness and ionization potential.
Machine learning modeling of all 8400 dipeptides and tripeptides indicated
that those with higher log P values and aliphatic
N/C-termini or aromatic C-termini were more likely to effectively
promote calcium absorption. These findings provide valuable insights
for the design of peptides to increase calcium bioavailability