Issue 17, 2024

Exploring pathological link between antimicrobial and amyloid peptides

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.

Graphical abstract: Exploring pathological link between antimicrobial and amyloid peptides

Article information

Article type
Review Article
Submitted
21 Jan 2024
First published
23 Jul 2024
This article is Open Access
Creative Commons BY license

Chem. Soc. Rev., 2024,53, 8713-8763

Exploring pathological link between antimicrobial and amyloid peptides

Y. Tang, Y. Zhang, D. Zhang, Y. Liu, R. Nussinov and J. Zheng, Chem. Soc. Rev., 2024, 53, 8713 DOI: 10.1039/D3CS00878A

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