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探索抗菌肽与淀粉样肽之间的病理联系。

Exploring pathological link between antimicrobial and amyloid peptides.

机构信息

Department of Chemical, Biomolecular, and Corrosion Engineering, The University of Akron, Ohio 44325, USA.

Division of Endocrinology and Diabetes, Department of Pediatrics, School of Medicine, Stanford University, Palo Alto, CA 94304, USA.

出版信息

Chem Soc Rev. 2024 Aug 27;53(17):8713-8763. doi: 10.1039/d3cs00878a.

Abstract

Amyloid peptides (AMYs) and antimicrobial peptides (AMPs) are considered as the two distinct families of peptides, characterized by their unique sequences, structures, biological functions, and specific pathological targets. However, accumulating evidence has revealed intriguing pathological connections between these peptide families in the context of microbial infection and neurodegenerative diseases. Some AMYs and AMPs share certain structural and functional characteristics, including the ability to self-assemble, the presence of β-sheet-rich structures, and membrane-disrupting mechanisms. These shared features enable AMYs to possess antimicrobial activity and AMPs to acquire amyloidogenic properties. Despite limited studies on AMYs-AMPs systems, the cross-seeding phenomenon between AMYs and AMPs has emerged as a crucial factor in the bidirectional communication between the pathogenesis of neurodegenerative diseases and host defense against microbial infections. In this review, we examine recent developments in the potential interplay between AMYs and AMPs, as well as their pathological implications for both infectious and neurodegenerative diseases. By discussing the current progress and challenges in this emerging field, this account aims to inspire further research and investments to enhance our understanding of the intricate molecular crosstalk between AMYs and AMPs. This knowledge holds great promise for the development of innovative therapies to combat both microbial infections and neurodegenerative disorders.

摘要

淀粉样肽(AMYs)和抗菌肽(AMPs)被认为是两类不同的肽家族,它们具有独特的序列、结构、生物学功能和特定的病理靶标。然而,越来越多的证据表明,在微生物感染和神经退行性疾病的背景下,这两种肽家族之间存在着有趣的病理联系。一些 AMYs 和 AMPs 具有某些结构和功能特征,包括自组装能力、富含β-折叠结构的存在以及破坏膜的机制。这些共同的特征使 AMYs 具有抗菌活性,使 AMPs 获得淀粉样特性。尽管对 AMYs-AMPs 系统的研究有限,但 AMYs 和 AMPs 之间的交叉成核现象已成为神经退行性疾病发病机制与宿主抵御微生物感染之间双向通讯的关键因素。在这篇综述中,我们研究了 AMYs 和 AMPs 之间潜在相互作用的最新进展,以及它们对感染性和神经退行性疾病的病理影响。通过讨论这个新兴领域的当前进展和挑战,本综述旨在激发更多的研究和投资,以增强我们对 AMYs 和 AMPs 之间复杂分子相互作用的理解。这一知识为开发创新疗法以对抗微生物感染和神经退行性疾病提供了巨大的潜力。

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