Researchers study protein biosynthesis in bacteria

Researchers study protein biosynthesis in bacteria
NusG couples transcription and translation. NusG binds to RNA polymerase via its NTD, and to the ribosome via its CTD. It thus serves as a flexible connection between the two machines. Credit: Philipp K. Zuber

Researchers of the University of Bayreuth and the Columbia University in New York reported groundbreaking findings on protein biosynthesis in bacteria in the journal iScience. The small protein NusG links the two large molecular machines that work together during gene expression, which is the production of bacterial proteins based on genetic information: RNA polymerase and the ribosome. The molecular bridge enables the bacterial cell to synchronize perfectly the successive stages of gene expression, i.e., transcription and translation. Thus, this connection could be an excellent target for future antibiotic drugs.

In all living organisms, gene expression is a two-stage process: First, the genetic information stored in the DNA is used as template to synthesize ribonucleic acids, so-called messenger RNAs (mRNAs). By this, is converted into a form that can be directly used by the cell. RNA polymerase is responsible for this process, which is called transcription. During the process of translation the messenger-RNAs, in turn, are the molecular blueprints that are read by the ribosome and used for the production of corresponding proteins. In humans and animals, these two stages of gene expression are separated both spatially and biochemically. In a bacterial cell, in contrast, they are coupled as scientists have known for more than 50 years.

Ten years ago, a research group at the University of Bayreuth led by Prof. Dr. Paul Rösch reported in Science first indications that this coupling might actually be mediated by the NusG. Yet only now has the research group led by Dr. Stefan H. Knauer, in cooperation with partners at Columbia University, New York, succeeded in providing the first direct structural evidence. NusG consists of two flexibly connected domains: an amino-terminal domain (NTD) and a carboxy-terminal domain (CTD). The CTD binds to the ribosome, the NTD to RNA polymerase. Thus, NusG forms a flexible bridge between the central machines of , similar to the movable coupling between railway wagons. This connection causes transcription and translation to be synchronized. Key experiments clearly showing this link were performed with high-resolution nuclear magnetic resonance (NMR) spectroscopy and which were carried out at the North Bavarian Center for High-Resolution NMR Spectroscopy at the University of Bayreuth.

"This opens up highly interesting perspectives for the development of new antibiotic agents. If we can disrupt this molecular bridge, bacterial protein synthesis and thus also reproduction of bacteria will be seriously impaired—most importantly, without affecting the human organism. We are targeting this approach in a current research project, and we have already achieved first promising results," says Dr. Stefan Knauer.

"We were able to demonstrate the central role of NusG in bacterial by combining structural biology, biochemical, and molecular biology methods. We will continue this in the search for efficient antibiotic substances," adds co-author Philipp Zuber M.Sc., who is doing his Ph.D. thesis at the University of Bayreuth, where he also completed the elite study program Macromolecular Science within the Elite Network of Bavaria.

The study published in iScience is the result of close cooperation between the Bayreuth researchers and the research groups of Prof. Dr. Max Gottesman and Prof. Dr. Joachim Frank at Columbia University in New York. Frank received the Nobel Prize in Chemistry in 2017 for his developments in cryoelectron microscopy, a research technology that was also used in the new study.


Explore further

Synthetic mRNAs modified with sulfur atoms boost efficient protein synthesis

More information: Robert S. Washburn et al. Escherichia coli NusG links the lead ribosome with the transcription elongation complex, iScience (2020). DOI: 10.1016/j.isci.2020.101352
Journal information: Science , iScience

Citation: Researchers study protein biosynthesis in bacteria (2020, July 21) retrieved 29 October 2020 from https://phys.org/news/2020-07-protein-biosynthesis-bacteria.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.
7 shares

Feedback to editors

User comments