A Review on Bacterial Cell division Protein and Recent Progress of FtsZ Inhibitors Development

被引:0
|
作者
Huang Xuan-He [1 ]
Sun Ning [2 ,3 ]
Zhong Dong-Xiao [1 ]
Chen Cui-Cui [1 ]
Li Ying [1 ]
Wong Wing-Leung [4 ]
Lu Yu-Jing [1 ]
机构
[1] Guangdong Univ Technol, Sch Biomed & Pharmaceut Sci, Guangzhou 510006, Peoples R China
[2] Hong Kong Polytech Univ, Dept Appl Biol Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Peoples R China
[3] Guangzhou Med Univ, Affiliated Hosp 5, Guangzhou 510700, Peoples R China
[4] Wuyi Univ, Sch Biotechnol & Hlth Sci, Jiangmen 529020, Peoples R China
关键词
drug resistance bacteria; antibacterial agents; cell division protein FtsZ; FtsZ inhibitors; ESCHERICHIA-COLI; ANTIBACTERIAL ACTIVITY; STAPHYLOCOCCUS-AUREUS; ASSEMBLY DYNAMICS; THIAZOLE ORANGE; PEPTIDOGLYCAN SYNTHESIS; CRYSTAL-STRUCTURES; GTPASE ACTIVITY; TARGETING FTSZ; SMALL-MOLECULE;
D O I
10.16476/j.pibb.2020.0055
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In recent years, the abuse of antibiotics has caused the emergence of drug-resistant bacteria, which is now widely spread around the world. It is currently a critical issue that seriously threats to human health due to the lack of effective clinical drugs to treat the multidrug-resistant bacterial infections. With such a serious shortage of drugs and means for clinical treatment against multidrug-resistant bacterial infections, it is urgently needed to develop new antibacterial drugs, especially those molecules possessing new mechanisms of action to combat the drug-resistant bacteria. Filamenting temperature-sensitive mutant Z (FtsZ) is an essential protein for bacterial division and has been one of the most popular targets for new drug discovery. FtsZ is a highly conserved protein and it plays a key role in cell division in most prokaryotic cells. In this article, we reviewed the structural characteristics and biological functions of bacterial cell division proteins and the recent research progress on antibacterial drugs development targeting FtsZ.
引用
收藏
页码:935 / 955
页数:21
相关论文
共 118 条
  • [1] The Antibacterial Cell Division Inhibitor PC190723 Is an FtsZ Polymer-stabilizing Agent That Induces Filament Assembly and Condensation
    Andreu, Jose M.
    Schaffner-Barbero, Claudia
    Huecas, Sonia
    Alonso, Dulce
    Lopez-Rodriguez, Maria L.
    Ruiz-Avila, Laura B.
    Nunez-Ramirez, Rafael
    Llorca, Oscar
    Martin-Galiano, Antonio J.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (19) : 14239 - 14246
  • [2] A diarylquinoline drug active on the ATP synthase of Mycobacterium tuberculosis
    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
    [J]. SCIENCE, 2005, 307 (5707) : 223 - 227
  • [3] Berezuk A M, 2018, SCI REPORTS, V8, P1
  • [4] FtsA G50E mutant suppresses the essential requirement for FtsK during bacterial cell division in Escherichia coli
    Berezuk, Alison M.
    Roach, Elyse J.
    Seidel, Laura
    Lo, Reggie Y.
    Khursigara, Cezar M.
    [J]. CANADIAN JOURNAL OF MICROBIOLOGY, 2020, 66 (04) : 313 - 327
  • [5] Sanguinarine blocks cytokinesis in bacteria by inhibiting FtsZ assembly and bundling
    Beuria, TK
    Santra, MK
    Panda, D
    [J]. BIOCHEMISTRY, 2005, 44 (50) : 16584 - 16593
  • [6] Promoting assembly and bundling of FtsZ as a strategy to inhibit bacterial cell division: a new approach for developing novel antibacterial drugs
    Beuria, Tushar K.
    Singh, Parminder
    Surolia, Avadhesha
    Panda, Dulal
    [J]. BIOCHEMICAL JOURNAL, 2009, 423 : 61 - 69
  • [7] Discovery of 1,3,4-oxadiazol-2-one-containing benzamide derivatives targeting FtsZ as highly potent agents of killing a variety of MDR bacteria strains
    Bi, Fangchao
    Song, Di
    Qin, Yinhui
    Liu, Xingbang
    Teng, Yuetai
    Zhang, Na
    Zhang, Panpan
    Zhang, Nan
    Ma, Shutao
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2019, 27 (14) : 3179 - 3193
  • [8] Design, synthesis and structure-based optimization of novel isoxazole-containing benzamide derivatives as FtsZ modulators
    Bi, Fangchao
    Song, Di
    Zhang, Nan
    Liu, Zhiyang
    Gu, Xinjie
    Hu, Chaoyu
    Cai, Xiaokang
    Venter, Henrietta
    Ma, Shutao
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2018, 159 : 90 - 103
  • [9] Design, synthesis and biological activity evaluation of novel 2,6-difluorobenzamide derivatives through FtsZ inhibition
    Bi, Fangchao
    Guo, Liwei
    Wang, Yinhu
    Venter, Henrietta
    Semple, Susan J.
    Liu, Fang
    Ma, Shutao
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2017, 27 (04) : 958 - 962
  • [10] Treadmilling by FtsZ filaments drives peptidoglycan synthesis and bacterial cell division
    Bisson-Filho, Alexandre W.
    Hsu, Yen-Pang
    Squyres, Georgia R.
    Kuru, Erkin
    Wu, Fabai
    Jukes, Calum
    Sun, Yingjie
    Dekker, Cees
    Holden, Seamus
    VanNieuwenhze, Michael S.
    Brun, Yves V.
    Garner, Ethan C.
    [J]. SCIENCE, 2017, 355 (6326) : 739 - 743