Sustainable synthesis of bakuchiol-mediated gold nanoparticles for drug delivery against bacterial strains and tumor microenvironments, and its in silico target proteins identification.

IF 3.9 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in Molecular Biosciences Pub Date : 2024-09-25 eCollection Date: 2024-01-01 DOI:10.3389/fmolb.2024.1469107
Pooja Mishra, Tabrez Faruqui, Sheeba Khanam, Mohd Khubaib, Irfan Ahmad, Mohd Saeed, Salman Khan
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Abstract

Introduction: The sustained synthesis of gold nanoparticles (GNPs) has gained significant attention in biomedical applications. In this study, we explored the antibacterial and anticancer potential of bakuchiol-mediated gold nanoparticles (Bak-GNPs). Bakuchiol, a natural compound found in Psoralea corylifolia seeds, serves as both a reducing and stabilizing agent for green synthesis of GNPs. Our objectives include network analysis, molecular docking, synthesis of GNPs, characterization, and antipathogenic and anticancer efficacy of Bak-GNPs against lung and liver cancers.

Methods: Protein-protein interaction networks were analyzed to identify effective protein targets for bakuchiol in lung and liver cancers. A molecular docking study was performed to validate the efficacy of the target protein against lung and liver cancer. Furthermore, Bak-GNPs were synthesized using bakuchiol and characterized by various techniques such as UV-visible spectroscopy, dynamic light scattering (DLS), zeta potential transmission electron microscopy (TEM), and Fourier-transform infrared (FTIR) spectroscopy, and their potential against pathogens and lung and liver cancers.

Results: GNAI3 emerged as the most promising target, with a binding energy of -7.5 kcal/mol compared to PTGER3's -6.9 kcal/mol, different characterization techniques revealed the successful synthesis of Bak-GNPs. Bak-GNPs exhibited potent antibacterial activity against both Gram-positive and Gram-negative bacteria, as confirmed by minimum inhibitory concentration (MIC) values. Bak-GNPs demonstrated significant anticancer effects on A549 (lung cancer) and HepG2 (liver cancer) cells, with IC50 values of 11.19 μg/mL and 6.6 μg/mL, respectively. Induction of apoptosis and inhibition of cell proliferation were observed in both the cell lines. The increased production of reactive oxygen species (ROS) contributes to its anticancer effects.

Discussion: This study highlights promising biomedical applications of bakuchiol-mediated GNPs. This green synthesis approach using bakuchiol provides a sustainable method for producing nanoparticles with enhanced biological activities. Further exploration of the pharmacological properties and mechanisms of Bak-GNPs is required to optimize their therapeutic efficacy for clinical use.

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可持续合成巴枯焦介导的金纳米颗粒,用于针对细菌菌株和肿瘤微环境的给药及其靶蛋白的硅学鉴定。
导言:金纳米粒子(GNPs)的持续合成在生物医学应用中备受关注。在本研究中,我们探索了以金纳米粒子(Bakuchiol)为介导的金纳米粒子(Bak-GNPs)的抗菌和抗癌潜力。Bakuchiol 是一种存在于榛子种子中的天然化合物,可作为还原剂和稳定剂用于 GNPs 的绿色合成。我们的目标包括网络分析、分子对接、GNPs 的合成、表征以及 Bak-GNPs 对肺癌和肝癌的抗病原性和抗癌功效:方法:分析蛋白质-蛋白质相互作用网络,以确定 Bakuchiol 在肺癌和肝癌中的有效蛋白质靶点。进行了分子对接研究,以验证靶蛋白对肺癌和肝癌的疗效。此外,研究人员还利用巴枯焦合成了Bak-GNPs,并通过紫外可见光谱、动态光散射(DLS)、ZETA电位透射电子显微镜(TEM)和傅立叶变换红外光谱(FTIR)等多种技术对其进行了表征,并研究了其对抗病原体、肺癌和肝癌的潜力:GNAI3是最有希望的靶点,其结合能为-7.5 kcal/mol,而PTGER3的结合能为-6.9 kcal/mol。最小抑菌浓度 (MIC) 值证实,Bak-GNPs 对革兰氏阳性菌和革兰氏阴性菌都具有很强的抗菌活性。Bak-GNPs 对 A549(肺癌)和 HepG2(肝癌)细胞具有显著的抗癌作用,IC50 值分别为 11.19 μg/mL 和 6.6 μg/mL。在这两种细胞系中都观察到了诱导细胞凋亡和抑制细胞增殖的作用。活性氧(ROS)的产生增加有助于其抗癌作用:本研究强调了巴枯酚介导的 GNPs 具有广阔的生物医学应用前景。这种使用巴枯焦的绿色合成方法为生产具有更强生物活性的纳米粒子提供了一种可持续的方法。需要进一步探索 Bak-GNPs 的药理特性和机制,以优化其临床应用的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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