In silico methods to identify meat-derived prolyl endopeptidase inhibitors

被引:65
|
作者
Lafarga, Tomas [1 ]
O'Connor, Paula [2 ]
Hayes, Maria [1 ]
机构
[1] TEAGASC, Irish Agr & Food Dev Author, Food BioSci Dept, Dublin, Ireland
[2] TEAGASC, Irish Agr & Food Dev Author, Food BioSci Dept, Fermoy, Cork, Ireland
关键词
In silica; Meat proteins; Meat by-products; Bioactive peptides; Prolyl endopeptidase; Mental health; DIPEPTIDYL PEPTIDASE-IV; BIOACTIVE PEPTIDES; CONVERTING-ENZYME; OLIGOPEPTIDASE; DRUG; PROTEINS; BINDING; PULSES;
D O I
10.1016/j.foodchem.2014.11.150
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
According to the World Health Organization (WHO), approximately 450 million people suffer from mental or neurological disorders and five of the ten leading causes of disability and premature death worldwide are psychiatric conditions. Social, biological and neurological sciences provided extensive understanding into the role of risk and protective factors in the development of mental disorders and poor mental health. Altered activity of a number of enzymes, such as prolyl endopeptidase (PEP, EC 3.4.21.26), has been linked to the prevention and treatment of a number of mental disorders, including anxiety, depression and Alzheimer's disease. The inhibition of PEP has potential for use in the prevention and in the treatment of mental disorders. The objective of this work was to identify PEP-inhibitory peptides from meat proteins using in silico methods. In this paper, five proteins commonly found in meat by-products were evaluated as a substrate for use in the generation of PEP inhibitory peptides. These include serum albumin, collagen and myosin. These proteins were cleaved in silica using BIOPEP and ExPASy PeptideCutter and the generated peptides were compared to known PEP-inhibiting peptides in the database of BIOPEP. A number of novel PEP inhibitory peptide sequences were identified in this study, including PPL, APPH, IPP and PPG with corresponding IC50 values of 2.86, 3.95, 4.02 and 2.70 mM, respectively. This work demonstrates the usefulness of in silico analysis for predicting the release of PEP-inhibiting peptides from meat proteins. (c) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:337 / 343
页数:7
相关论文
共 31 条
  • [21] Ligand- and structure-based in silico studies to identify kinesin spindle protein (KSP) inhibitors as potential anticancer agents
    Balakumar, Chandrasekaran
    Ramesh, Muthusamy
    Tham, Chuin Lean
    Khathi, Samukelisiwe Pretty
    Kozielski, Frank
    Srinivasulu, Cherukupalli
    Hampannavar, Girish A.
    Sayyad, Nisar
    Soliman, Mahmoud E.
    Karpoormath, Rajshekhar
    JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2018, 36 (14) : 3687 - 3704
  • [22] Investigating a Library of Flavonoids as Potential Inhibitors of a Cancer Therapeutic Target MEK2 Using in Silico Methods
    AlZahrani, Wejdan M. M.
    AlGhamdi, Shareefa A. A.
    Sohrab, Sayed S. S.
    Rehan, Mohd
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (05)
  • [23] Identification of Bioactive Peptides from a Laminaria digitata Protein Hydrolysate Using In Silico and In Vitro Methods to Identify Angiotensin-1-Converting Enzyme (ACE-1) Inhibitory Peptides
    Purcell, Diane
    Packer, Michael A. A.
    Hayes, Maria
    MARINE DRUGS, 2023, 21 (02)
  • [24] Peptides Derived from Soy and Lupin Protein as Dipeptidyl-Peptidase IV Inhibitors: In Vitro Biochemical Screening and in Silico Molecular Modeling Study
    Lammi, Carmen
    Zanoni, Chiara
    Arnoldi, Anna
    Vistoli, Giulio
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2016, 64 (51) : 9601 - 9606
  • [25] Structure based virtual screening to identify the beta-lactamase CTX-M-9 inhibitors: An in silico effort to overcome antibiotic resistance in E. coli
    Davari, Kambiz
    Nowroozi, Jamileh
    Hosseini, Farzaneh
    Sepahy, Abbas Akhavan
    Mirzaie, Sako
    COMPUTATIONAL BIOLOGY AND CHEMISTRY, 2017, 67 : 174 - 181
  • [26] Develop a High-Throughput Screening Method to Identify C-P4H1 (Collagen Prolyl 4-Hydroxylase 1) Inhibitors from FDA-Approved Chemicals
    Wang, Shike
    Lee, Kuo-Hao
    Araujo, Nathalia Victoria
    Zhan, Chang-Guo
    Rangnekar, Vivek M.
    Xu, Ren
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (18) : 1 - 13
  • [27] 4,4-Nitrophenoxyaniline derived Azo ester: Structural elucidation, DFT simulation, and DNA interactional studies via wet and in silico methods
    Qamar, Samina
    Perveen, Fouzia
    Akhter, Zareen
    Yousuf, Sammer
    Sultan, Muhammd
    Ela, Sule Erten
    Ullah, Naimat
    Fatima, Kalsoom
    Kanwal, Sehrish
    JOURNAL OF MOLECULAR STRUCTURE, 2022, 1250
  • [28] LY3041658/ interleukin-8 complex structure as targets for IL-8 small molecule inhibitors discovery using a combination of in silico methods
    Tran, T. T. N.
    Tran, Q. H.
    Nguyen, Q. T.
    Le, M. T.
    Trinh, D. T. T.
    Tran, V. H.
    Thai, K. M.
    SAR AND QSAR IN ENVIRONMENTAL RESEARCH, 2022, 33 (10) : 753 - 778
  • [29] The identification of novel inhibitors of human angiotensin-converting enzyme 2 and main protease of Sars-Cov-2: A combination of in silico methods for treatment of COVID-19
    Zarezade, Vahid
    Rezaei, Hamzeh
    Shakerinezhad, Ghodratollah
    Safavi, Arman
    Nazeri, Zahra
    Veisi, Ali
    Azadbakht, Omid
    Hatami, Mahdi
    Sabaghan, Mohamad
    Shajirat, Zeinab
    JOURNAL OF MOLECULAR STRUCTURE, 2021, 1237
  • [30] Sulfonyl hydrazones derived from 3-formylchromone as non-selective inhibitors of MAO-A and MAO-B: Synthesis, molecular modelling and in-silico ADME evaluation
    Abid, Syed Mobasher Ali
    Younus, Hafiza Amna
    Al-Rashida, Mariya
    Arshad, Zunaira
    Maryum, Tooba
    Gilani, Mazhar Amjad
    Alharthi, Abdulrahman I.
    Iqbal, Jamshed
    BIOORGANIC CHEMISTRY, 2017, 75 : 291 - 302