Folic acid delivery by serum proteins: loading efficacy and protein morphology

J Biomol Struct Dyn. 2017 Dec;35(16):3499-3506. doi: 10.1080/07391102.2016.1259589. Epub 2016 Nov 25.

Abstract

The loading efficacy of folic acid with serum proteins human serum albumin (HSA), bovine serum albumin (BSA), and beta-lactoglobulin (β-LG) was analyzed and the effect of acid conjugation on protein morphology was determined. Structural analysis showed that folic acid binds HSA, BSA, and β-LG via hydrophilic, hydrophobic, and H-bonding contacts with BSA forming more stable conjugates than HSA and β-LG. Molecular modeling showed the presence of several H-bonding systems, stabilizing acid-protein conjugates. Folic acid conjugation alters protein conformation by major alterations of α-helix and β-sheet. TEM images showed major protein morphological changes inducing protein aggregation upon acid interaction. The results show that serum proteins can deliver folic acid to target molecules.

Keywords: BSA; HSA; TEM; delivery; folic acid; modeling; morphology; β-LG.

MeSH terms

  • Animals
  • Binding Sites
  • Cattle
  • Folic Acid / chemistry*
  • Humans
  • Hydrogen Bonding
  • Hydrophobic and Hydrophilic Interactions
  • Kinetics
  • Lactoglobulins / chemistry*
  • Molecular Docking Simulation
  • Protein Aggregates
  • Protein Binding
  • Protein Conformation, alpha-Helical
  • Protein Conformation, beta-Strand
  • Protein Interaction Domains and Motifs
  • Serum Albumin, Bovine / chemistry*
  • Serum Albumin, Human / chemistry*
  • Thermodynamics

Substances

  • Lactoglobulins
  • Protein Aggregates
  • Serum Albumin, Bovine
  • Folic Acid
  • Serum Albumin, Human