Abstract

Riboswitches reside in the untranslated region of RNA and regulate genes involved in the biosynthesis of essential metabolites through binding of small molecules. Since their discovery at the beginning of this century, riboswitches have been regarded as potential antibacterial targets. Using fragment screening, high-throughput screening and rational ligand design guided by X-ray crystallography, lead compounds against various riboswitches have been identified. Here, we review the current status and suitability of the thiamine pyrophosphate (TPP), flavin mononucleotide (FMN), glmS, guanine, and other riboswitches as antibacterial targets and discuss them in a biological context. Further, we highlight challenges in riboswitch drug discovery and emphasis the need to develop riboswitch specific high-throughput screening methods.

Highlights

  • The flavin mononucleotide (FMN) riboswitch is the one that has been most explored as an antibacterial target

  • The discovery of ribocil C is probably the most important contribution to the field, as it established the possibility of targeting a riboswitch with synthetic ligands having chemically distinct scaffold as compared to their natural ligands

  • Another interesting contribution to exploring riboswitches as antibacterial drug targets is the invention of 5FDQD, which demonstrated that negatively charged groups could be replaced with hydrophobic moieties without compromising the affinity

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Summary

Introduction

In downstream gene expression (open reading frame (ORF), marked in yellow) These riboswitches most cases, binding of ligand to transcriptional and/or termination are known as “OFF-switches”. In the case of translation regu- are known as gene expression (open reading frame (ORF), marked in yellow) These riboswitches lation, the RBS (green box) is either sequestered (a) or released (b) upon ligand binding. The thiamine pyrophosphate (TPP) riboswitch is the most prevalent riboswitch and is the only one present in eukaryotes, including algae [18], fungi [19,20,21] and plants [22,23] These natural ligands span a wide spectrum of man bacterial pathogens and are suitable targets for broad-spectrum antibiotics, phosphorylated sugars).

Prevalence of riboswitches riboswitches inprevalently
TPP Riboswitch Ligands
G19. The pyrophosphate hydrogen bonds with to polar of G40 and
FMN Riboswitch Ligands
Guanine Riboswitch Ligands
Guanine
General Considerations for Riboswitch Drug Discovery
Fragment-Based Screening
Structure-Based Virtual Screening
Findings
Conclusions
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