Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

The rapid emergence of multi-drug-resistant bacteria has raised a serious public health concern. Therefore, new antibiotic developments have been highly desired. Here, we propose a new method to visualize antibiotic actions on translating ribosomes in the cell-free system under macromolecular crowding conditions by cryo-electron microscopy, designated as the DARC method: the Direct visualization of Antibiotic binding on Ribosomes in the Cell-free translation system. This new method allows for acquiring a more comprehensive understanding of the mode of action of antibiotics on the translation inhibition without ribosome purification. Furthermore, with the direct link to biochemical analysis at the same condition as cryo-EM observation, we revealed the evolution of 2-DOS aminoglycosides from dibekacin (DBK) to arbekacin (ABK) by acquiring the synthetic tailored anchoring motif to lead to stronger binding affinity to ribosomes. Our cryo-EM structures of DBK and ABK bound ribosomes in the cell-free environment clearly depicted a synthetic tailored γ-amino-α-hydroxybutyryl (HABA) motif formed additional interactions with the ribosome enhancing antibiotic bindings. This new approach would be valuable for understanding the function of antibiotics for more efficient drug development.

Download full-text PDF

Source
http://dx.doi.org/10.1093/jb/mvae002DOI Listing

Publication Analysis

Top Keywords

ribosomes cell-free
16
direct visualization
8
cell-free system
8
synthetic tailored
8
ribosomes
5
visualization ribosomes
4
cell-free
4
system revealed
4
revealed functional
4
functional evolution
4

Similar Publications

Refinement of OnePot PURE and Crude Ribosome Production for Reproducible Cell-free Protein Synthesis.

J Vis Exp

August 2025

Centre for Engineering Biology, Institute of Quantitative Biology, Biochemistry and Biotechnology, School of Biological Sciences, University of Edinburgh;

Recent advances have enabled the Protein synthesis Using Recombinant Elements (PURE) cell-free system to be produced in individual laboratories economically and with reduced labor burden. However, the preparation of the 36 protein components and ribosome, which make up PURE, is still a complex undertaking, with much scope for variation and error. We present a detailed and updated procedure to manufacture PURE based on the recently published OnePot protocol, which involves regulating a number of key steps, in particular, the inoculation of cultures using optical density (OD)-normalized glycerol stocks, careful monitoring of cell growth, and controlling final glycerol concentrations.

View Article and Find Full Text PDF

Viruses have evolved elaborate mechanisms to hijack the host mRNA translation machinery to direct viral protein synthesis. Picornaviruses, whose RNA genome lacks a cap structure, inhibit cap-dependent mRNA translation, and utilize an internal ribosome entry site (IRES) in the RNA 5' untranslated region to recruit the 40S ribosomal subunit. IRES activity is stimulated by a set of host proteins termed IRES -acting factors (ITAFs).

View Article and Find Full Text PDF

Background: Alterations of the circulating microbiota have recently been implicated in the pathogenesis of cardiometabolic disease. However, the evidence is based primarily on bacterial DNA signatures, while the characteristics and roles of circulating fungal DNA signatures (mycobiota) remain unknown.

Methods: In a nationwide prospective cohort of 960 hemodialysis patients, we characterized circulating cell-free mycobiota signatures in baseline serum samples using internal transcribed spacer (ITS) ribosomal DNA (rDNA) sequencing and examined their associations with all-cause and cardiovascular mortality using Cox models with adjustment for potential confounders.

View Article and Find Full Text PDF

Post-translational modifications (PTMs) are important for the stability and function of many therapeutic proteins and peptides. Current methods for studying and engineering PTMs are often limited by low-throughput experimental techniques. Here we describe a generalizable, in vitro workflow coupling cell-free gene expression (CFE) with AlphaLISA for the rapid expression and testing of PTM installing proteins.

View Article and Find Full Text PDF

Marine plankton communities consist of numerous species, and their composition and physiological states are closely linked to ecosystem functions. Understanding biogeochemical cycles requires measuring taxon-specific mortality due to viral lysis, sloppy feeding, and other mechanical stresses as the dissolved organic matter released contributes to rapid nutrient recycling and long-term carbon sequestration following microbial transformation. To examine the lytic cell death of marine microeukaryotes, we applied a quantitative and comprehensive analysis of the dissolved constituents of seawater using the Mortality by Ribosomal Sequencing (MoRS) method.

View Article and Find Full Text PDF