Umami Peptides Screened Based on Peptidomics and Virtual Screening from Ruditapes philippinarum and Mactra veneriformis Clams

[Display omitted] •Screening method of umami peptides based on peptidomics and virtual screening.•Peptide length and positive control were considered during screening.•His121, Ser146, Ser123, Tyr143 and Gly144 in T1R3 were the main binding sites. The existing technology used for screening umami pept...

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Veröffentlicht in:Food chemistry 2022-11, Vol.394, p.133504-133504, Article 133504
Hauptverfasser: Zhang, Ting, Hua, Ying, Zhou, Changyu, Xiong, Yongzhao, Pan, Daodong, Liu, Zhu, Dang, Yali
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container_start_page 133504
container_title Food chemistry
container_volume 394
creator Zhang, Ting
Hua, Ying
Zhou, Changyu
Xiong, Yongzhao
Pan, Daodong
Liu, Zhu
Dang, Yali
description [Display omitted] •Screening method of umami peptides based on peptidomics and virtual screening.•Peptide length and positive control were considered during screening.•His121, Ser146, Ser123, Tyr143 and Gly144 in T1R3 were the main binding sites. The existing technology used for screening umami peptides is time-consuming and labor-intensive, making it difficult to meet the requirements of rapid screening of peptides. In this study, a high-throughput screening method for umami peptides was established based on peptidomics and virtual screening including the mass spectrometry, iUmami-SCM, PeptideRanker, and T1R1/T1R3 receptor. Subsequently, they were characterized and validated using sensory evaluation and electronic tongue. Results showed that 18 potential umami peptides were screened from two clams. Among them, 16 peptides had umami characteristics with thresholds range 0.123-1.481 mmol/L, and the accuracy of the screening method was about 88.9%. Additionally, active sites such as Tyr143, Gly144, Ser146, Ala145, His121, Ser123, and Glu277 may play a critical role in flavor presentation by molecular docking with T1R1/T1R3. The paper could provide a fast and reliable method for screening umami peptides as well as lay the foundation for novel strategies for evaluating umami taste.
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The existing technology used for screening umami peptides is time-consuming and labor-intensive, making it difficult to meet the requirements of rapid screening of peptides. In this study, a high-throughput screening method for umami peptides was established based on peptidomics and virtual screening including the mass spectrometry, iUmami-SCM, PeptideRanker, and T1R1/T1R3 receptor. Subsequently, they were characterized and validated using sensory evaluation and electronic tongue. Results showed that 18 potential umami peptides were screened from two clams. Among them, 16 peptides had umami characteristics with thresholds range 0.123-1.481 mmol/L, and the accuracy of the screening method was about 88.9%. Additionally, active sites such as Tyr143, Gly144, Ser146, Ala145, His121, Ser123, and Glu277 may play a critical role in flavor presentation by molecular docking with T1R1/T1R3. 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The existing technology used for screening umami peptides is time-consuming and labor-intensive, making it difficult to meet the requirements of rapid screening of peptides. In this study, a high-throughput screening method for umami peptides was established based on peptidomics and virtual screening including the mass spectrometry, iUmami-SCM, PeptideRanker, and T1R1/T1R3 receptor. Subsequently, they were characterized and validated using sensory evaluation and electronic tongue. Results showed that 18 potential umami peptides were screened from two clams. Among them, 16 peptides had umami characteristics with thresholds range 0.123-1.481 mmol/L, and the accuracy of the screening method was about 88.9%. Additionally, active sites such as Tyr143, Gly144, Ser146, Ala145, His121, Ser123, and Glu277 may play a critical role in flavor presentation by molecular docking with T1R1/T1R3. 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source ScienceDirect Journals (5 years ago - present)
subjects clams
peptidomics
screening
umami peptides
virtual screening
title Umami Peptides Screened Based on Peptidomics and Virtual Screening from Ruditapes philippinarum and Mactra veneriformis Clams
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