Physicochemical, medicinal chemistry, and ADMET characteristics of bee antimicrobial peptides as natural bio-preservatives to extend food shelf life: a roadmap for food safety regulation.

IF 2.7 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Biomolecular Structure & Dynamics Pub Date : 2024-11-21 DOI:10.1080/07391102.2024.2429181
Roy Dinata, Chettri Arati, Ahmed-Laskar Saeed, Bose Manikandan, Giri Abinash, Buragohain Pori, Rema Momin Bidanchi, Vikas Kumar Roy, Guruswami Gurusubramanian
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Abstract

Antimicrobial peptides (AMPs) are gaining popularity as potential substitutes for conventional antibiotics and bio-preservatives in response to an increase in antimicrobial resistance cases. However, their poor pharmacokinetic profiles limit their applicability. This study using ADMETlab, OECD QSAR toolbox, and VEGA HUB virtual environments profiled 82 peptide sequences of seven bee antimicrobial peptides (BAMPs: abaecin, apamin, apisimin, apidaecin, defensin, hymenoptaecin, and melittin) using 81 descriptors combining physicochemical, medicinal chemistry, ADMET, and toxicophore criteria. BAMPs adhere to key drug-like physicochemical features and drug-ability regulations set forth by pharmaceutical giants, including Lipinski, Pfizer, and GlaxoSmithKline. BAMPs have been predicted to demonstrate favorable cell permeability, high water solubility, oral bioavailability, no blood-brain barrier penetration, oral and intestinal absorption, excretion, and a high therapeutic index. They function as non-substrates of p-glycoprotein and do not alter the pharmacokinetic effects of P-gp substrates. None of BAMPs were found to inhibit cytochrome P450 enzymes, indicating their potential to promote drug clearance and metabolism. BAMPs are safe from adverse reactions, free of respiratory toxicity, hERG blockers, hepatotoxicity, sensitizers, carcinogens, and mutagens. They are non-corrosive, non-irritating to the eyes, non-bioaccumulative, non-ecotoxic, antibacterial, antifungal, and antiviral, low toxic with no toxicophore or PAINS alerts recorded. They are non-toxic to various receptors, including gonadal and stress receptors, PPAR-γ, mitochondrial membrane receptor, heat shock element, and p53. Seven BAMPs have been tested for their drug-like properties, supporting their potential as potential leads for the pharmaceutical and food industries as antimicrobial agents and bio-preservatives. Future studies should optimize bee peptide expression in biological systems.

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作为延长食品保质期的天然生物防腐剂的蜜蜂抗菌肽的物理化学、药物化学和 ADMET 特性:食品安全监管路线图。
随着抗菌素耐药性的增加,抗菌肽作为传统抗生素和生物防腐剂的潜在替代品越来越受欢迎。然而,其不良的药代动力学特征限制了其适用性。本研究利用 ADMETlab、OECD QSAR 工具箱和 VEGA HUB 虚拟环境,结合物理化学、药物化学、ADMET 和毒物学标准,使用 81 个描述符对七种蜜蜂抗菌肽(BAMPs:abaecin、apamin、apisimin、apidaecin、defensin、hymenoptaecin 和 melittin)的 82 个肽序列进行了分析。BAMPs 符合包括利宾斯基、辉瑞和葛兰素史克在内的制药巨头制定的关键类药物理化特征和可药性规定。据预测,BAMPs 具有良好的细胞渗透性、高水溶性、口服生物利用度、无血脑屏障渗透、口腔和肠道吸收、排泄和高治疗指数。它们的功能是非 p-glycoprotein 底物,不会改变 P-gp 底物的药代动力学效应。没有发现任何一种 BAMPs 会抑制细胞色素 P450 酶,这表明它们具有促进药物清除和代谢的潜力。BAMPs 不会产生不良反应,不含呼吸道毒性、hERG 阻断剂、肝毒性、致敏剂、致癌物和致突变物。它们不腐蚀、不刺激眼睛、无生物蓄积性、无ecotoxic、抗菌、抗真菌和抗病毒,毒性低,没有毒物或 PAINS 警报记录。它们对各种受体无毒,包括性腺和应激受体、PPAR-γ、线粒体膜受体、热休克素和 p53。已对七种 BAMPs 进行了类药物特性测试,支持其作为抗菌剂和生物防腐剂应用于制药和食品工业的潜力。未来的研究应优化蜂肽在生物系统中的表达。
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来源期刊
Journal of Biomolecular Structure & Dynamics
Journal of Biomolecular Structure & Dynamics 生物-生化与分子生物学
CiteScore
8.90
自引率
9.10%
发文量
597
审稿时长
2 months
期刊介绍: The Journal of Biomolecular Structure and Dynamics welcomes manuscripts on biological structure, dynamics, interactions and expression. The Journal is one of the leading publications in high end computational science, atomic structural biology, bioinformatics, virtual drug design, genomics and biological networks.
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