Characterization of ACE Inhibitory Peptides fromMactra veneriformis Hydrolysate by Nano-Liquid Chromatography Electrospray Ionization MassSpectrometry (Nano-LC-ESI-MS) and Molecular Docking

Marine Drugs

Jiao Chen¹  Rui Liu²  Xinzhi Wang²  Hao Wu²  Lingchong Wang²  Yunhan Zhu²  Lei Shi² 

[1] China Pharmaceutical University, Nanjing, Jiangsu 210009, China;Jiangsu Key Laboratory of Research and Development in Marine Bio-resource Pharmaceutics, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210023, China;

关键词: ACE inhibitory peptide;    characterization;    nano-LC-MS/MS;    molecular docking;    Mactra veneriformis;   

DOI  :  10.3390/md12073917

来源: DOAJ

【 摘 要 】

Food-derived bioactive compounds are gaining increasing significancein life sciences. In the present study, we identified angiotensin I-converting enzyme(ACE)-inhibitory peptides from Mactra veneriformis hydrolysate using a nano-LC-MS/MS method. Mactra veneriformis hydrolysate was first separated into four fractions (F1–F4) based on molecular weight by ultrafiltration. The fraction with molecular weight lower than 1 kDa (F1) showed the highest ACE inhibitory activity. F1 was then analyzed by a high throughput nano-LC-MS/MS method and sequences of peptides in F1 were calculated accordingly. The 27 peptides identified as above were chemically synthesized and tested for ACE-inhibitory activity. The hexapeptide VVCVPW showed the highest potency with an IC50 value of 4.07 μM. We then investigated the interaction mechanism between the six most potent peptides and ACE by molecular docking. Our docking results suggested that the ACE inhibitory peptides bind to ACE via interactions with His383, His387, and Glu411 residues. Particularly, similar to the thiol group of captopril, the cysteine thiol group of the most potent peptide VVCVPW may play a key role in the binding of this peptide to the ACE active site.

【 授权许可】

Unknown