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靶向蛋白质紊乱以修复抗菌药物耐药性

Targeting Protein Disorder for the Remediation of Antimicrobial Resistance.

作者信息

Callaghan Jack O', Ryan Michael P, Hudson Sarah, Thompson Damien

机构信息

Department of Physics, Bernal Institute, University of Limerick, Limerick V94 T9PX, Ireland.

Bernal Institute, University of Limerick, Limerick V94 T9PX, Ireland.

出版信息

ACS Omega. 2024 Dec 10;9(51):50589-50598. doi: 10.1021/acsomega.4c08427. eCollection 2024 Dec 24.

Abstract

The remediation of antimicrobial resistance (AMR) is a fundamental challenge for global healthcare. Intrinsically disordered proteins (IDPs) are recognized drug targets for neurodegeneration and cancer but have not been considered to date for AMR. Here, a novel link between structural disorder and AMR is identified by mapping predicted disorder profiles onto existing transcriptomic data for resistant and susceptible isolates. The AMR-relevant IDPs fall into two distinct classes, those involved in the bacterial stress response and those differentially expressed between resistant and susceptible strains following antibiotic exposure. A residue-wise conservation analysis of relevant bacterial IDPs identified mutations within intrinsically disordered regions that correlate with pronounced changes in antimicrobial susceptibility, providing valuable insight into the functional importance of bacterial intrinsic disorder in the ESKAPEE pathogens. The identification of susceptibility-inducing IDPs in highlights the potential of disorder-based antimicrobial drug discovery for the remediation of drug-resistant bacterial infections.

摘要

抗微生物药物耐药性(AMR)的补救是全球医疗保健面临的一项根本性挑战。内在无序蛋白(IDP)是公认的神经退行性疾病和癌症的药物靶点,但迄今为止尚未被考虑用于AMR。在这里,通过将预测的无序谱映射到耐药和敏感分离株的现有转录组数据上,确定了结构无序与AMR之间的新联系。与AMR相关的IDP分为两个不同的类别,一类参与细菌应激反应,另一类在抗生素暴露后在耐药和敏感菌株之间差异表达。对相关细菌IDP进行的逐残基保守性分析确定了内在无序区域内与抗菌敏感性的显著变化相关的突变,这为ESKAPEE病原体中细菌内在无序的功能重要性提供了有价值的见解。在[具体内容未提及]中诱导敏感性的IDP的鉴定突出了基于无序的抗菌药物发现对于补救耐药细菌感染的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e10f/11683595/f75d2e4d8535/ao4c08427_0001.jpg

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