Structural and biochemical analysis of ObgE, a central regulator of bacterial persistence.

TitleStructural and biochemical analysis of ObgE, a central regulator of bacterial persistence.
Publication TypeJournal Article
Year of Publication2017
AuthorsGkekas, S., R. Kumar Singh, A. V. Shkumatov, J. Messens, M. Fauvart, N. Verstraeten, J. Michiels, and W. Versées
JournalJ Biol Chem
Volume292
Issue14
Pagination5871-5883
Date Published2017 04 07
ISSN1083-351X
KeywordsCations, Monovalent, Crystallography, X-Ray, Escherichia coli, Escherichia coli Proteins, Monomeric GTP-Binding Proteins, Potassium, Protein Domains, Protein Multimerization
Abstract

The Obg protein family belongs to the TRAFAC (translation factor) class of P-loop GTPases and is conserved from bacteria to eukaryotes. Essential roles in many different cellular processes have been suggested for the Obg protein from (ObgE), and we recently showed that it is a central regulator of bacterial persistence. Here, we report the first crystal structure of ObgE at 1.85-Å resolution in the GDP-bound state, showing the characteristic N-terminal domain and a central G domain that are common to all Obg proteins. ObgE also contains an intrinsically disordered C-terminal domain, and we show here that this domain specifically contributed to GTP binding, whereas it did not influence GDP binding or GTP hydrolysis. Biophysical analysis, using small angle X-ray scattering and multi-angle light scattering experiments, revealed that ObgE is a monomer in solution, regardless of the bound nucleotide. In contrast to recent suggestions, our biochemical analyses further indicate that ObgE is neither activated by K ions nor by homodimerization. However, the ObgE GTPase activity was stimulated upon binding to the ribosome, confirming the ribosome-dependent GTPase activity of the Obg family. Combined, our data represent an important step toward further unraveling the detailed molecular mechanism of ObgE, which might pave the way to further studies into how this GTPase regulates bacterial physiology, including persistence.

DOI10.1074/jbc.M116.761809
Alternate JournalJ. Biol. Chem.
PubMed ID28223358
PubMed Central IDPMC5392579
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