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Peptides with Dual Antimicrobial–Anticancer Activity: Strategies to Overcome Peptide Limitations and Rational Design of Anticancer Peptides

机译:肽与双抗菌 - 抗癌活动:克服肽局限性的策略和抗癌肽的理性设计

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摘要

Peptides are naturally produced by all organisms and exhibit a wide range of physiological, immunomodulatory, and wound healing functions. Furthermore, they can provide with protection against microorganisms and tumor cells. Their multifaceted performance, high selectivity, and reduced toxicity have positioned them as effective therapeutic agents, representing a positive economic impact for pharmaceutical companies. Currently, efforts have been made to invest in the development of new peptides with antimicrobial and anticancer properties, but the poor stability of these molecules in physiological environments has triggered a bottleneck. Therefore, some tools, such as nanotechnology and in silico approaches can be applied as alternatives to try to overcome these obstacles. In silico studies provide a priori knowledge that can lead to the development of new anticancer peptides with enhanced biological activity and improved stability. This review focuses on the current status of research in peptides with dual antimicrobial–anticancer activity, including advances in computational biology using in silico analyses as a powerful tool for the study and rational design of these types of peptides.
机译:肽是由所有生物体天然产生的,并且具有广泛的生理,免疫调节和伤口愈合功能。此外,它们可以提供针对微生物和肿瘤细胞的保护。它们的多方面性能,高选择性和降低的毒性使其定位为有效的治疗剂,代表了制药公司的积极经济影响。目前,已经努力投资于具有抗微生物和抗癌性质的新肽的发展,但是这些分子在生理环境中的稳定性较差引发了瓶颈。因此,可以将一些工具(如纳米技术和硅方法)应用于尝试克服这些障碍的替代方案。在硅研究中,提供了先验的知识,可以导致具有增强的生物活性和改善的稳定性的新抗癌肽的发展。本综述重点介绍了双抗微生物 - 抗癌活动的肽研究现状,包括在硅中使用计算生物学的进步,分析为这些类型肽的研究和合理设计的强大工具。

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