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反义抗生素的化学策略。

Chemical strategies for antisense antibiotics.

机构信息

Institute for Molecules and Materials, Radboud University Nijmegen, the Netherlands. Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands.

出版信息

Chem Soc Rev. 2024 Nov 25;53(23):11303-11320. doi: 10.1039/d4cs00238e.

Abstract

Antibacterial resistance is a severe threat to modern medicine and human health. To stay ahead of constantly-evolving bacteria we need to expand our arsenal of effective antibiotics. As such, antisense therapy is an attractive approach. The programmability allows to in principle target any RNA sequence within bacteria, enabling tremendous selectivity. In this Tutorial Review we provide guidelines for devising effective antibacterial antisense agents and offer a concise perspective for future research. We will review the chemical architectures of antibacterial antisense agents with a special focus on the delivery and target selection for successful antisense design. This Tutorial Review will strive to serve as an essential guide for antibacterial antisense technology development.

摘要

抗菌耐药性是现代医学和人类健康的严重威胁。为了抵御不断进化的细菌,我们需要扩大有效的抗生素库。因此,反义疗法是一种有吸引力的方法。可编程性使得原则上可以靶向细菌内的任何 RNA 序列,从而实现极高的选择性。在本教程综述中,我们提供了设计有效抗菌反义药物的指导方针,并为未来的研究提供了简明的观点。我们将回顾具有特殊重点的抗菌反义药物的化学结构,用于成功的反义设计的递药和靶标选择。本教程综述将努力成为抗菌反义技术发展的重要指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a3/11495246/788d0a93ef6a/d4cs00238e-f1.jpg

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