4
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Targeting bacterial central metabolism for drug development.

      1 , 2 , 3
      Chemistry & biology

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Current antibiotics, derived mainly from natural sources, inhibit a narrow spectrum of cellular processes, namely DNA replication, protein synthesis, and cell wall biosynthesis. With the worldwide explosion of drug resistance, there is renewed interest in the investigation of alternate essential cellular processes, including bacterial central metabolic pathways, as a drug target space for the next generation of antibiotics. However, the validation of targets in central metabolism is more complex, as essentiality of such targets can be conditional and/or contextual. Bearing in mind our enhanced understanding of prokaryotic central metabolism, a key question arises: can central metabolism be bacteria's Achilles' heel and a therapeutic target for the development of new classes of antibiotics? In this review, we draw lessons from oncology and attempt to address some of the open questions related to feasibility of targeting bacterial central metabolism as a strategy for developing new antibacterial drugs.

          Related collections

          Author and article information

          Journal
          Chem. Biol.
          Chemistry & biology
          1879-1301
          1074-5521
          Nov 20 2014
          : 21
          : 11
          Affiliations
          [1 ] Laboratory of Microbiology and Microsystems, Global Health Institute, Swiss Federal Institute of Technology (EPFL), EPFL/SV/GHI/UPKIN, Station 19, 1015 Lausanne, Switzerland. Electronic address: paul.murima@epfl.ch.
          [2 ] Laboratory of Microbiology and Microsystems, Global Health Institute, Swiss Federal Institute of Technology (EPFL), EPFL/SV/GHI/UPKIN, Station 19, 1015 Lausanne, Switzerland.
          [3 ] Antibacterial Drug Discovery Unit, Institute Pasteur Korea, Sampyeong-dong 696, South Korea; Lee Kong Chian School of Medicine and School of Biological Sciences, Nanyang Technological University, Proteos, 61 Biopolis Drive, Singapore 138673, Singapore. Electronic address: kevin.pethe@ntu.edu.sg.
          Article
          S1074-5521(14)00324-X
          10.1016/j.chembiol.2014.08.020
          25442374
          8edccb03-232d-4b9f-8ad6-457a7c72ef7a
          Copyright © 2014 Elsevier Ltd. All rights reserved.
          History

          Comments

          Comment on this article