Identification and virtual screening of novel salty peptides from hydrolysate of tilapia by-product by batch molecular docking

被引:8
|
作者
Ren, Hongjun [1 ]
Zhou, Jingxuan [1 ]
Fu, Huixian [1 ]
Feng, Qiaohui [1 ]
Wang, Jionghao [1 ]
Li, Chuan [1 ,2 ,3 ]
Xia, Guanghua [1 ,2 ,3 ]
Shang, Wenting [1 ]
He, Yanfu [1 ,2 ,3 ]
机构
[1] Hainan Univ, Coll Food Sci & Engn, Haikou, Peoples R China
[2] Hainan Prov Engn Res Ctr Aquat Resources Efficient, Haikou, Peoples R China
[3] Key Lab Seafood Proc Haikou, Haikou, Peoples R China
来源
FRONTIERS IN NUTRITION | 2024年 / 10卷
关键词
tilapia by-product hydrolysate; salty peptide; salt receptor; TRPV1; virtual screening; molecular docking; TRPV1; CHANNEL; TASTE;
D O I
10.3389/fnut.2023.1343209
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Introduction Tilapia produces a large number of by-products during processing, which contain potentially flavorful peptides.Methods The application of PyRx software enabled batch molecular docking andscreening of 16 potential salty peptides from 189 peptides identified in the enzymaticdigestion of tilapia by-products.Results According to sensory analysis, all 16 peptides werepredominantly salty with a threshold of 0.256 - 0.379 mmol/L with some sournessand astringency, among which HLDDALR had the highest salty intensity, followedby VIEPLDIGDDKVR, FPGIPDHL, and DFKSPDDPSRH. I addition, moleculardocking results showed these four core peptides with high salt intensity bound to thesalt receptor TRPV1 mainly via van der Waals interactions, hydrogen bonds, andhydrophobic forces; Arg491, Tyr487, VAL441, and Asp708 were the key sites for thebinding of salty peptides to TRPV1. Therefore, the application of batch moleculardocking using PyRx is effective and economical for the virtual screening of saltypeptides.
引用
收藏
页数:9
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