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揭示基于方酰胺的阴离子载体的强大抗菌活性——氯离子转运与膜破坏

Uncovering the potent antimicrobial activity of squaramide based anionophores - chloride transport and membrane disruption.

作者信息

Brennan Luke E, Luo Xuanyang, Mohammed Farhad Ali, Kavanagh Kevin, Elmes Robert B P

机构信息

Department of Chemistry, Maynooth University Maynooth Co. Kildare Ireland.

Synthesis and Solid-State Pharmaceutical Centre (SSPC) Ireland.

出版信息

Chem Sci. 2025 Jan 22;16(9):4075-4084. doi: 10.1039/d4sc01693a. eCollection 2025 Feb 26.

Abstract

Antimicrobial resistance (AMR) - often referred to as a silent pandemic, is at present the most serious threat to medicine, and with constantly emerging resistance to novel drugs, combined with the paucity of their development, is likely to worsen. To circumvent this, supramolecular chemists have proposed the applicability of synthetic anion transporters in the fight against AMR. In this article we discuss the synthesis, supramolecular characterisation and biological profiling of six structurally simple squaramide anion transporters. Through a combination of spectroscopic techniques, and cellular assays we have deduced the mode of action of these antimicrobial agents to be as a result of both anion transport and membrane disruption. Furthermore, through the synthesis of two fluorescent analogues we verified this membrane-localised activity using Super-Resolution nanoscopy methods. These compounds represent particularly active antimicrobial anionophores and compliment similar reports showing the applicability of agents such as these in the fight against AMR.

摘要

抗菌耐药性(AMR)——常被称为一场无声的大流行,目前是医学面临的最严重威胁。随着对新型药物的耐药性不断出现,再加上新型药物研发的匮乏,情况可能会恶化。为了规避这一问题,超分子化学家提出了合成阴离子转运体在对抗AMR中的适用性。在本文中,我们讨论了六种结构简单的方酰胺阴离子转运体的合成、超分子表征和生物学分析。通过光谱技术和细胞分析相结合,我们推断这些抗菌剂的作用方式是阴离子转运和膜破坏的结果。此外,通过合成两种荧光类似物,我们使用超分辨率纳米显微镜方法验证了这种膜定位活性。这些化合物代表了特别活跃的抗菌阴离子载体,并补充了类似的报告,表明此类药剂在对抗AMR中的适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb78/11863690/80c0d006a856/d4sc01693a-s1.jpg

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