利用分子对接和动力学模拟从天麻煎剂和配方颗粒中鉴定哮喘中的 NF-κB 抑制肽

IF 0.7 4区 医学 Q4 PHARMACOLOGY & PHARMACY Current Pharmaceutical Analysis Pub Date : 2024-04-03 DOI:10.2174/0115734129298587240322073956
Xiaotong Xiao, Yaxiong Liu, Yayang Huang, Wenjie Zeng, Zhuoya Luo
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引用次数: 0

摘要

背景:Pheretima aspergillum煎剂是一种传统的治疗形式,而配方颗粒则是通过传统中药煎剂生产的。然而,白僵菌中的有效成分尚未完全阐明,也没有公开报道对白僵菌水煎剂和配方颗粒之间的差异进行研究。研究目的本研究旨在探索天麻煎剂和配方颗粒中潜在的生物活性肽,并研究其通过与 IκBβ/NF-κB p65 复合物相互作用来缓解哮喘相关炎症的潜在药理机制。方法:采用μLC-Q Exactive MS与全新测序技术相结合,鉴定天麻煎剂和配方颗粒中潜在的生物活性肽。利用深度学习模型评估了这些肽的生物活性和毒性。进一步的研究包括分子对接研究,旨在揭示所选多肽与 IκBβ/NF-κB p65 复合物在亲和力和关键残基位点上的相互作用。分子动力学模拟评估了肽受体复合物的稳定性。研究结果从天麻煎剂中鉴定出2235个肽段,从天麻配方颗粒中鉴定出1424个肽段。通过深度学习模型,从煎剂中鉴定出 298 种生物活性肽和无毒肽,从配方颗粒中鉴定出 145 种生物活性肽和无毒肽。分子对接显示,煎剂中的 160 种肽和配方颗粒中的 63 种肽与 IκBβ/NF-κB p65 复合物具有很强的亲和力。分子动力学模拟结果表明,煎剂中的肽 EGPANFADLGK 和配方颗粒中的肽 KAAVDFGVPGDAGALAHLK 与 IκBβ/NF-κB p65 复合物的相互作用具有稳定性。总之,在天麻煎剂和配方颗粒中都发现了潜在的生物活性肽。结论本研究通过 IκBβ/NF-κB p65 复合物的相互作用,探讨了从天麻煎剂和配方颗粒中提取的肽在缓解哮喘相关炎症方面的潜在药理机制,为阐明治疗哮喘的分子作用机制提供了依据。
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Identification of the NF-κB Inhibition Peptides in Asthma from Pheretima aspergillum Decoction and Formula Granules Using Molecular Docking and Dynamics Simulations
Background: The Pheretima aspergillum decoction is a traditional therapeutic form, while the formula granules are produced through traditional Chinese medicine decoctions. However, the active ingredients in Pheretima aspergillum have not been fully elucidated, and no published reports have investigated the differences between Pheretima aspergillum decoction and formula granules. Objective: The study aimed to explore the potential bioactive peptides in Pheretima aspergillum decoction and formula granules and investigate their potential pharmacological mechanisms in alleviating inflammation associated with asthma through interaction with the IκBβ/NF-κB p65 complex. Methods: μLC-Q Exactive MS combined with de novo sequencing technology was employed to identify potential bioactive peptides in Pheretima aspergillum decoction and formula granules. Deep learning models were utilized to evaluate the bioactivity and toxicity of these peptides. Further investigations included molecular docking studies aimed at uncovering the interactions between the selected peptides and the IκBβ/NF-κB p65 complex at affinity and critical residue sites. Molecular dynamics simulations were conducted to assess the stability of the peptide-receptor complexes. Results: A total of 2,235 peptides from the Pheretima aspergillum decoction and 1,424 peptides from the Pheretima aspergillum formula granules were identified. Deep learning models resulted in the identification of 298 bioactive and non-toxic peptides from the decoction and 145 from the formula granules. Molecular docking revealed that 160 peptides from the decoction and 63 from the formula granules exhibited a strong affinity for the IκBβ/NF-κB p65 complex. The results of molecular dynamics simulations supported the stability of the interactions involving the peptide EGPANFADLGK from the decoction and the peptide KAAVDFGVPGDAGALAHLK from the formula granules with the IκBβ/NF-κB p65 complex. In conclusion, potential bioactive peptides were identified in both Pheretima aspergillum decoction and formula granules. Conclusion: This study has investigated the potential pharmacological mechanisms of peptides derived from Pheretima aspergillum decoction and formula granules in alleviating inflammation associated with asthma through the interaction of the IκBβ/NF-κB p65 complex, providing a basis for elucidating the molecular mechanism of action for the treatment of asthma.
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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
85
审稿时长
3 months
期刊介绍: Aims & Scope Current Pharmaceutical Analysis publishes expert reviews and original research articles on all the most recent advances in pharmaceutical and biomedical analysis. All aspects of the field are represented including drug analysis, analytical methodology and instrumentation. The journal is essential to all involved in pharmaceutical, biochemical and clinical analysis.
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