期刊
FOOD BIOPHYSICS
卷 15, 期 2, 页码 162-172出版社
SPRINGER
DOI: 10.1007/s11483-019-09616-9
关键词
ACE inhibitory activity; Food bioactive peptides; Molecular docking; Protein-ligand interactions
资金
- Brazilian agency CAPES
- Brazilian agency CNPq
- Brazilian agency FAPEMIG
- Brazilian agency FINEP
- Brazilian agency FUNARBE
- Brazilian agency SisNANO/MCTI
- CNPq
Hypertension is nowadays one of the major world concerns in public health. Several food proteins, among which caseins, can be substrates for generating peptides with antihypertensive potential. With the increasingly evolution of computational tools, in silico molecular modeling have gained prominence in studies of protein-ligand complexes in different research fields, such as pharmaceutics and biochemical engineering. However, the application of such methodologies in food-related research can be considered still embryonic. Thus, the central aim of the present work was to apply molecular modelling in order to elucidate the molecular bases of the anti-hypertensive potential of milk caseins-derived peptides. Firstly, hydrolysates obtained from a controlled trypsinolysis of caseins were fractioned according to their molecular weight, by ultrafiltration and RP-HPLC. The obtained fractions were evaluated with regard to their in vitro inhibitory angiotensin-converting enzyme activity (%I-ACE). Six chromatographic fractions were identified, and three of them displayed high ACE-inhibition (F-1: 80.68%; F-2: 79.00%; and F-4: 62.44%). Finally, intermolecular interactions networks in complexes formed between ACE and the identified peptides were assessed through in silico molecular docking. At the molecular level, a correlation between in vitro and in silico results was found: the peptides FFVAPFPEVFGK (F-6), FALPQYLK (F-2, F-4) and ALNEINQFYQK (F-1) presented the lowest biding energies and interacted by specific H-bonds, electrostatic and hydrophobic interactions formed within ACE active site S1 residues (Ala354, Glu384, and Tyr 523) and the Zn2+ coordinated residues (His383, His387, and Glu411). The fraction F-3, despite its low total peptide concentration, presented a moderate inhibitory activity for ACE (49.2%), likely due to H-bonds between HQGLPQEVLNENLLR and the active site S1 residues.
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