Ribosome-associated proteins in fungal ribosome homeostasis: Conceptual opportunities for peptide-based modulation.

IF 3.8 4区 生物学 Q2 MICROBIOLOGY
Journal of Microbiology Pub Date : 2026-03-01 Epub Date: 2026-02-24 DOI:10.71150/jm.2511006
Yongjun Kim, Chang-Jun Ji, Seohyun Park, Junsuk Lee, Jiwoon Jung, Yejin Kim, Dabin Pyeon, Yoon-Mo Yang
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引用次数: 0

Abstract

Ribosomes are essential macromolecular machines that facilitate protein synthesis and have long been recognized as effective targets for antimicrobial agents. While structural differences between prokaryotic and eukaryotic ribosomes form the basis for selective antibiotics against bacteria, similar approaches for developing antifungal agents targeting ribosomes have remained limited due to the high sequence and structural conservation with human ribosomes. However, emerging insights into ribosome homeostasis, including ribosome biogenesis, turnover, and hibernation, have uncovered a set of ribosome-associated proteins whose function is critical yet display greater sequence divergence from their human counterparts. These observations suggest that these regulatory components may represent viable antifungal targets by disrupting fungal proteostasis. The present review aims to explore this developing concept by examining ribosome-associated factors and considering whether short ribosomal protein-derived peptides may eventually serve as druggable molecules for selectively modulating these pathways in fungal pathogens.

真菌核糖体稳态中的核糖体相关蛋白:基于肽的调节的概念机会。
核糖体是促进蛋白质合成的重要大分子机器,长期以来一直被认为是抗菌药物的有效靶点。虽然原核生物和真核生物核糖体之间的结构差异构成了针对细菌的选择性抗生素的基础,但由于与人类核糖体的高序列和结构保守性,开发针对核糖体的抗真菌药物的类似方法仍然有限。然而,对核糖体动态平衡的新见解,包括核糖体的生物发生、周转和冬眠,已经发现了一组核糖体相关蛋白,其功能至关重要,但与人类的对应蛋白显示出更大的序列差异。这些观察结果表明,这些调节成分可能通过破坏真菌的蛋白酶平衡来代表可行的抗真菌靶点。本综述旨在通过检查核糖体相关因素和考虑短核糖体蛋白衍生肽是否最终可能作为选择性调节真菌病原体中这些途径的药物分子来探索这一发展中的概念。
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
Journal of Microbiology
Journal of Microbiology 生物-微生物学
CiteScore
5.70
自引率
3.30%
发文量
0
审稿时长
3 months
期刊介绍: Publishes papers that deal with research on microorganisms, including archaea, bacteria, yeasts, fungi, microalgae, protozoa, and simple eukaryotic microorganisms. Topics considered for publication include Microbial Systematics, Evolutionary Microbiology, Microbial Ecology, Environmental Microbiology, Microbial Genetics, Genomics, Molecular Biology, Microbial Physiology, Biochemistry, Microbial Pathogenesis, Host-Microbe Interaction, Systems Microbiology, Synthetic Microbiology, Bioinformatics and Virology. Manuscripts dealing with simple identification of microorganism(s), cloning of a known gene and its expression in a microbial host, and clinical statistics will not be considered for publication by JM.
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