Abstract
The discovery and use of antibacterials represents a primary success of modern pharmaceutical industry. However, the pace of antibacterial discovery was heavily hindered by a series of technical difficulties and the unfavorable economics in recent years. The past decade has witnessed rapid progresses in omics and systems biology, which provided an unprecedented opportunity to accelerate the discovery of antibacterials. In this article, we first summarize the successful use of metabolic network analysis in antibacterial discovery. Then, we reveal that metabolite concentration serves as a useful criterion for selecting antimicrobial targets. The essential enzymes with low substrate concentrations (< 0.5 mM) are more druggable antibacterial targets. Besides, we find that the solubility of clinically used competitive antibacterials is at least 100 times higher than the concentrations of the competed substrates. By the new-proposed criterion, we not only identify some promising antibacterial targets but also explain some perplexing experimental observations as well.
Keywords: Antibacterial discovery, antibacterial target, bioinformatics, flux balance analysis (FBA), metabolic network, metabolite concentration, metabolomics, systems biology.
Current Computer-Aided Drug Design
Title:Metabolite Concentration as a Criterion for Antibacterial Discovery
Volume: 9 Issue: 3
Author(s): Zhong-Yi Wang, Qiang Zhu and Hong-Yu Zhang
Affiliation:
Keywords: Antibacterial discovery, antibacterial target, bioinformatics, flux balance analysis (FBA), metabolic network, metabolite concentration, metabolomics, systems biology.
Abstract: The discovery and use of antibacterials represents a primary success of modern pharmaceutical industry. However, the pace of antibacterial discovery was heavily hindered by a series of technical difficulties and the unfavorable economics in recent years. The past decade has witnessed rapid progresses in omics and systems biology, which provided an unprecedented opportunity to accelerate the discovery of antibacterials. In this article, we first summarize the successful use of metabolic network analysis in antibacterial discovery. Then, we reveal that metabolite concentration serves as a useful criterion for selecting antimicrobial targets. The essential enzymes with low substrate concentrations (< 0.5 mM) are more druggable antibacterial targets. Besides, we find that the solubility of clinically used competitive antibacterials is at least 100 times higher than the concentrations of the competed substrates. By the new-proposed criterion, we not only identify some promising antibacterial targets but also explain some perplexing experimental observations as well.
Export Options
About this article
Cite this article as:
Wang Zhong-Yi, Zhu Qiang and Zhang Hong-Yu, Metabolite Concentration as a Criterion for Antibacterial Discovery, Current Computer-Aided Drug Design 2013; 9 (3) . https://dx.doi.org/10.2174/15734099113099990030
DOI https://dx.doi.org/10.2174/15734099113099990030 |
Print ISSN 1573-4099 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6697 |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers
Related Articles
-
Biologic Therapy in Psoriasis: Safety Profile
Current Drug Safety Prevalence of Adverse Drug Reactions to Highly Active Antiretroviral Therapy (HAART) among HIV Positive Patients in Imam Khomeini Hospital of Tehran, Iran
Infectious Disorders - Drug Targets Synthesis of Gold Mediated Biocompatible Nanocomposite of Lactone Enriched Fraction from Sahadevi (Vernonia cinerea Lees): An Assessment of Antimalarial Potential
Current Topics in Medicinal Chemistry Pharmacogenomics in Drug Induced Liver Injury
Current Drug Metabolism Recent Trends on the Development of Machine Learning Approaches for the Prediction of Lysine Acetylation Sites
Current Medicinal Chemistry Editorial (Thematic Issue: Iron Chelation and Drug Resistance in Cancer and Tuberculosis)
Current Pharmaceutical Biotechnology Slow-Onset Inhibition of 2-trans-Enoyl-ACP (CoA) Reductase from Mycobacterium tuberculosis by an Inorganic Complex
Current Pharmaceutical Design Deubiquitinating Enzymes as Promising Drug Targets for Infectious Diseases
Current Pharmaceutical Design Nanoparticles vs Cancer: A Multifuncional Tool
Current Topics in Medicinal Chemistry Advances in Synthesis and Medicinal Applications of Compounds Derived from Phthalimide
Current Organic Synthesis Is Anticoagulation with Novel Oral Anticoagulants an Effective Treatment for Tuberculosis Patients not Achieving a Therapeutic Range with Vitamin K Antagonists? A Systematic Review
Cardiovascular & Hematological Disorders-Drug Targets Allopurinol and Loss of Consciousness in a 78-old Year Man Suffering from Gout
Infectious Disorders - Drug Targets The TLR4 ASP299GLY Polymorphism is a Risk Factor for Active Tuberculosis in Caucasian HIV-Infected Patients
Current HIV Research Development and Implementation of the DHAPP Military eHealth Information Network System
Current HIV Research The Role of Macrophages in Rheumatoid Arthritis
Current Pharmaceutical Design Why is the Incidence of Type 1 Diabetes Increasing?
Current Diabetes Reviews Hydrolases in Organic Chemistry. Recent Achievements in the Synthesis of Pharmaceuticals
Current Organic Chemistry Rapid Analysis of Pharmacology for Infectious Diseases
Current Topics in Medicinal Chemistry Premature Ageing Prevention: Limitations and Perspectives of Pharmacological Interventions
Current Drug Targets The Chemical Composition and Anti-mycobacterial Activities of <i>Trachyspermum copticum</i> and <i>Pelargonium graveolens</i> Essential Oils
Recent Patents on Anti-Infective Drug Discovery