Bacterial cell division proteins as antibiotic targets - PubMed (original) (raw)
Review
Bacterial cell division proteins as antibiotic targets
Tanneke den Blaauwen et al. Bioorg Chem. 2014 Aug.
Abstract
Proteins involved in bacterial cell division often do not have a counterpart in eukaryotic cells and they are essential for the survival of the bacteria. The genetic accessibility of many bacterial species in combination with the Green Fluorescence Protein revolution to study localization of proteins and the availability of crystal structures has increased our knowledge on bacterial cell division considerably in this century. Consequently, bacterial cell division proteins are more and more recognized as potential new antibiotic targets. An international effort to find small molecules that inhibit the cell division initiating protein FtsZ has yielded many compounds of which some are promising as leads for preclinical use. The essential transglycosylase activity of peptidoglycan synthases has recently become accessible to inhibitor screening. Enzymatic assays for and structural information on essential integral membrane proteins such as MraY and FtsW involved in lipid II (the peptidoglycan building block precursor) biosynthesis have put these proteins on the list of potential new targets. This review summarises and discusses the results and approaches to the development of lead compounds that inhibit bacterial cell division.
Keywords: Antimicrobials; Bacterial cell division; ClpP; Divisome; EnvC; FtsA; FtsB; FtsEX; FtsL; FtsQ; FtsW; FtsZ; MraY; Mur; PcsB; Penicillin Binding Proteins; Translgycolysase activity; ZipA.
Copyright © 2014 Elsevier Inc. All rights reserved.
Similar articles
- Do the divisome and elongasome share a common evolutionary past?
Szwedziak P, Löwe J. Szwedziak P, et al. Curr Opin Microbiol. 2013 Dec;16(6):745-51. doi: 10.1016/j.mib.2013.09.003. Epub 2013 Oct 1. Curr Opin Microbiol. 2013. PMID: 24094808 Review. - Targeting the assembly of bacterial cell division protein FtsZ with small molecules.
Schaffner-Barbero C, Martín-Fontecha M, Chacón P, Andreu JM. Schaffner-Barbero C, et al. ACS Chem Biol. 2012 Feb 17;7(2):269-77. doi: 10.1021/cb2003626. Epub 2011 Nov 15. ACS Chem Biol. 2012. PMID: 22047077 Review. - A model for the Escherichia coli FtsB/FtsL/FtsQ cell division complex.
Villanelo F, Ordenes A, Brunet J, Lagos R, Monasterio O. Villanelo F, et al. BMC Struct Biol. 2011 Jun 14;11:28. doi: 10.1186/1472-6807-11-28. BMC Struct Biol. 2011. PMID: 21672257 Free PMC article. - Advances in the discovery of novel antimicrobials targeting the assembly of bacterial cell division protein FtsZ.
Li X, Ma S. Li X, et al. Eur J Med Chem. 2015 May 5;95:1-15. doi: 10.1016/j.ejmech.2015.03.026. Epub 2015 Mar 14. Eur J Med Chem. 2015. PMID: 25791674 Review. - An oldie but a goodie - cell wall biosynthesis as antibiotic target pathway.
Schneider T, Sahl HG. Schneider T, et al. Int J Med Microbiol. 2010 Feb;300(2-3):161-9. doi: 10.1016/j.ijmm.2009.10.005. Epub 2009 Dec 14. Int J Med Microbiol. 2010. PMID: 20005776 Review.
Cited by
- Targeting the FtsZ Allosteric Binding Site with a Novel Fluorescence Polarization Screen, Cytological and Structural Approaches for Antibacterial Discovery.
Huecas S, Araújo-Bazán L, Ruiz FM, Ruiz-Ávila LB, Martínez RF, Escobar-Peña A, Artola M, Vázquez-Villa H, Martín-Fontecha M, Fernández-Tornero C, López-Rodríguez ML, Andreu JM. Huecas S, et al. J Med Chem. 2021 May 13;64(9):5730-5745. doi: 10.1021/acs.jmedchem.0c02207. Epub 2021 Apr 28. J Med Chem. 2021. PMID: 33908781 Free PMC article. - Antimicrobial Susceptibility Testing: A Comprehensive Review of Currently Used Methods.
Gajic I, Kabic J, Kekic D, Jovicevic M, Milenkovic M, Mitic Culafic D, Trudic A, Ranin L, Opavski N. Gajic I, et al. Antibiotics (Basel). 2022 Mar 23;11(4):427. doi: 10.3390/antibiotics11040427. Antibiotics (Basel). 2022. PMID: 35453179 Free PMC article. Review. - The structural assembly switch of cell division protein FtsZ probed with fluorescent allosteric inhibitors.
Artola M, Ruíz-Avila LB, Ramírez-Aportela E, Martínez RF, Araujo-Bazán L, Vázquez-Villa H, Martín-Fontecha M, Oliva MA, Martín-Galiano AJ, Chacón P, López-Rodríguez ML, Andreu JM, Huecas S. Artola M, et al. Chem Sci. 2017 Feb 1;8(2):1525-1534. doi: 10.1039/c6sc03792e. Epub 2016 Oct 21. Chem Sci. 2017. PMID: 28616148 Free PMC article. - Selective Inhibition of Neisseria gonorrhoeae by a Dithiazoline in Mixed Infections with Lactobacillus gasseri.
Lenz JD, Shirk KA, Jolicoeur A, Dillard JP. Lenz JD, et al. Antimicrob Agents Chemother. 2018 Nov 26;62(12):e00826-18. doi: 10.1128/AAC.00826-18. Print 2018 Dec. Antimicrob Agents Chemother. 2018. PMID: 30275084 Free PMC article. - Computational Identification of Essential Enzymes as Potential Drug Targets in Shigella flexneri Pathogenesis Using Metabolic Pathway Analysis and Epitope Mapping.
Narad P, Himanshu, Bansal H. Narad P, et al. J Microbiol Biotechnol. 2021 Apr 28;31(4):621-629. doi: 10.4014/jmb.2007.07006. J Microbiol Biotechnol. 2021. PMID: 33323673 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical