Targeting Bacterial Central Metabolism for Drug Development

被引:146
作者
Murima, Paul [1 ]
McKinney, John D. [1 ]
Pethe, Kevin [2 ,3 ,4 ]
机构
[1] Swiss Fed Inst Technol EPFL, EPFL SV GHI UPKIN, Global Hlth Inst, Lab Microbiol & Microsyst, CH-1015 Lausanne, Switzerland
[2] Inst Pasteur Korea, Antibacterial Drug Discovery Unit, Songnam, Gyeonggi Do, South Korea
[3] Nanyang Technol Univ, Lee Kong Chian Sch Med, Singapore 138673, Singapore
[4] Nanyang Technol Univ, Sch Biol Sci, Singapore 138673, Singapore
来源
CHEMISTRY & BIOLOGY | 2014年 / 21卷 / 11期
基金
新加坡国家研究基金会;
关键词
NONREPLICATING MYCOBACTERIUM-TUBERCULOSIS; PARA-AMINOSALICYLIC ACID; PYRUVATE-KINASE M2; ATP SYNTHASE; DIHYDROFOLATE-REDUCTASE; STAPHYLOCOCCUS-AUREUS; CANCER METABOLISM; ANTIBACTERIAL DISCOVERY; POSTANTIBIOTIC ERA; CARBON METABOLISM;
D O I
10.1016/j.chembiol.2014.08.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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.
引用
收藏
页码:1423 / 1432
页数:10
相关论文
共 120 条
[1]
Pathway-Selective Sensitization of Mycobacterium tuberculosis for Target-Based Whole-Cell Screening [J].
Abrahams, Garth L. ;
Kumar, Anuradha ;
Savvi, Suzana ;
Hung, Alvin W. ;
Wen, Shijun ;
Abell, Chris ;
Barry, Clifton E., III ;
Sherman, David R. ;
Boshoff, Helena I. M. ;
Mizrahi, Valerie .
CHEMISTRY & BIOLOGY, 2012, 19 (07) :844-854
[2]
Resistance to antibiotics: Are we in the post-antibiotic era? [J].
Alanis, AJ .
ARCHIVES OF MEDICAL RESEARCH, 2005, 36 (06) :697-705
[3]
Metabolite-enabled eradication of bacterial persisters by aminoglycosides [J].
Allison, Kyle R. ;
Brynildsen, Mark P. ;
Collins, James J. .
NATURE, 2011, 473 (7346) :216-+
[4]
Pyruvate kinase M2 activators promote tetramer formation and suppress tumorigenesis [J].
Anastasiou, Dimitrios ;
Yu, Yimin ;
Israelsen, William J. ;
Jiang, Jian-Kang ;
Boxer, Matthew B. ;
Hong, Bum Soo ;
Tempel, Wolfram ;
Dimov, Svetoslav ;
Shen, Min ;
Jha, Abhishek ;
Yang, Hua ;
Mattaini, Katherine R. ;
Metallo, Christian M. ;
Fiske, Brian P. ;
Courtney, Kevin D. ;
Malstrom, Scott ;
Khan, Tahsin M. ;
Kung, Charles ;
Skoumbourdis, Amanda P. ;
Veith, Henrike ;
Southall, Noel ;
Walsh, Martin J. ;
Brimacombe, Kyle R. ;
Leister, William ;
Lunt, Sophia Y. ;
Johnson, Zachary R. ;
Yen, Katharine E. ;
Kunii, Kaiko ;
Davidson, Shawn M. ;
Christofk, Heather R. ;
Austin, Christopher P. ;
Inglese, James ;
Harris, Marian H. ;
Asara, John M. ;
Stephanopoulos, Gregory ;
Salituro, Francesco G. ;
Jin, Shengfang ;
Dang, Lenny ;
Auld, Douglas S. ;
Park, Hee-Won ;
Cantley, Lewis C. ;
Thomas, Craig J. ;
Heiden, Matthew G. Vander .
NATURE CHEMICAL BIOLOGY, 2012, 8 (10) :839-847
[5]
Inhibition of Pyruvate Kinase M2 by Reactive Oxygen Species Contributes to Cellular Antioxidant Responses [J].
Anastasiou, Dimitrios ;
Poulogiannis, George ;
Asara, John M. ;
Boxer, Matthew B. ;
Jiang, Jian-kang ;
Shen, Min ;
Bellinger, Gary ;
Sasaki, Atsuo T. ;
Locasale, Jason W. ;
Auld, Douglas S. ;
Thomas, Craig J. ;
Vander Heiden, Matthew G. ;
Cantley, Lewis C. .
SCIENCE, 2011, 334 (6060) :1278-1283
[6]
A diarylquinoline drug active on the ATP synthase of Mycobacterium tuberculosis [J].
Andries, K ;
Verhasselt, P ;
Guillemont, J ;
Göhlmann, HWH ;
Neefs, JM ;
Winkler, H ;
Van Gestel, J ;
Timmerman, P ;
Zhu, M ;
Lee, E ;
Williams, P ;
de Chaffoy, D ;
Huitric, E ;
Hoffner, S ;
Cambau, E ;
Truffot-Pernot, C ;
Lounis, N ;
Jarlier, V .
SCIENCE, 2005, 307 (5707) :223-227
[7]
BASIS OF SELECTIVITY OF ANTIBACTERIAL DIAMINOPYRIMIDINES [J].
BACCANARI, DP ;
KUYPER, LF .
JOURNAL OF CHEMOTHERAPY, 1993, 5 (06) :393-399
[8]
Metabolic Regulation of Mycobacterial Growth and Antibiotic Sensitivity [J].
Baek, Seung-Hun ;
Li, Alice H. ;
Sassetti, Christopher M. .
PLOS BIOLOGY, 2011, 9 (05)
[9]
Bacterial persistence as a phenotypic switch [J].
Balaban, NQ ;
Merrin, J ;
Chait, R ;
Kowalik, L ;
Leibler, S .
SCIENCE, 2004, 305 (5690) :1622-1625
[10]
Barry C.E., 2009, SPECTRUM LATENT TUBE, P1