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基于核糖开关的高通量筛选方法的抗菌药物发现。

Riboswitch-based antibacterial drug discovery using high-throughput screening methods.

机构信息

Sofia University "St. Kliment Ohridski", Department of Genetics, Sofia, Bulgaria.

出版信息

Expert Opin Drug Discov. 2013 Jan;8(1):65-82. doi: 10.1517/17460441.2013.740455. Epub 2012 Nov 20.

Abstract

INTRODUCTION

Bacterial riboswitches are structured RNA domains usually residing at the 5' untranslated region of messenger RNAs that can directly bind specific metabolites. They serve as logic gates regulating gene expression. As a result, riboswitches enable mRNAs to regulate their own expression without the need for any regulatory proteins. The first riboswitches were found just 10 years ago. Over the last decade, more than dozen different riboswitch classes were identified in many bacterial species, and their number is still growing. These findings indicate that bacteria widely use RNA switches to sense changes in cell physiology and to regulate metabolic pathways.

AREAS COVERED

The authors discuss the main mechanisms for riboswitch control of gene expression in bacteria. Various riboswitch classes were found in human bacterial pathogens to control the synthesis of essential cell metabolites as discussed in this review. Some riboswitches can be used as novel targets for antibacterial drug discovery. This review presents the current and possible future high-throughput screening approaches for targeting riboswitches in the process of drug development.

EXPERT OPINION

Bacterial riboswitches of 17 different classes are discovered in 36 human bacterial pathogens that can be targeted for addressing the ever-growing need for new antibiotics. In this regard, the adaptation of various in silico, in vitro, and in vivo high-throughput screening methods for probing specific RNA switches are crucial for the success of antibacterial drug discovery process.

摘要

简介

细菌的核糖体开关是位于信使 RNA 5'非翻译区的结构 RNA 结构域,能够直接结合特定的代谢物。它们充当逻辑门,调节基因表达。因此,核糖体开关使 mRNA 能够在不需要任何调节蛋白的情况下调节自身的表达。第一个核糖体开关是在 10 年前发现的。在过去的十年中,在许多细菌物种中发现了超过十几种不同的核糖体开关类,并且这个数字还在不断增加。这些发现表明,细菌广泛使用 RNA 开关来感知细胞生理学的变化,并调节代谢途径。

涵盖领域

作者讨论了细菌中核糖体开关控制基因表达的主要机制。在本综述中讨论了在人类细菌病原体中发现的各种核糖体开关类,用于控制必需细胞代谢物的合成。一些核糖体开关可以用作新型抗菌药物发现的靶标。本综述介绍了目前和未来可能用于药物开发过程中靶向核糖体开关的高通量筛选方法。

专家意见

在 36 种人类细菌病原体中发现了 17 种不同类别的细菌核糖体开关,可以作为解决新抗生素需求不断增长的靶标。在这方面,适应各种用于探测特定 RNA 开关的计算、体外和体内高通量筛选方法对于抗菌药物发现过程的成功至关重要。

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