Recent advances in research of colchicine binding site inhibitors and their interaction modes with tubulin

Author(s):  
Kewei Sun ◽  
Zhonghao Sun ◽  
Fenglan Zhao ◽  
Guangzhi Shan ◽  
Qingguo Meng

Microtubules have been a concerning target of cancer chemotherapeutics for decades, and several tubulin-targeted agents, such as paclitaxel, vincristine and vinorelbine, have been approved. The colchicine binding site is one of the primary targets on microtubules and possesses advantages compared with other tubulin-targeted agents, such as inhibitors of tumor vessels and overcoming P-glycoprotein overexpression-mediated multidrug resistance. This study reviews and summarizes colchicine binding site inhibitors reported in recent years with structural studies via the crystal structures of complexes or computer simulations to discover new lead compounds. We are attempting to resolve the challenge of colchicine site agent research.

RSC Advances ◽  
2021 ◽  
Vol 11 (31) ◽  
pp. 18938-18944
Author(s):  
Jia-Hong Lei ◽  
Ling-Ling Ma ◽  
Jing-Hong Xian ◽  
Hai Chen ◽  
Jian-Jian Zhou ◽  
...  

Crystal structures of tubulin complexed with ELR510444 and parbendazole facilitate the design of novel colchicine binding site inhibitors.


2017 ◽  
Vol 139 ◽  
pp. 792-803 ◽  
Author(s):  
Giuseppe Felice Mangiatordi ◽  
Daniela Trisciuzzi ◽  
Domenico Alberga ◽  
Nunzio Denora ◽  
Rosa Maria Iacobazzi ◽  
...  

2017 ◽  
Vol 114 (28) ◽  
pp. 7355-7360 ◽  
Author(s):  
Simon Arragain ◽  
Ornella Bimai ◽  
Pierre Legrand ◽  
Sylvain Caillat ◽  
Jean-Luc Ravanat ◽  
...  

Sulfur is present in several nucleosides within tRNAs. In particular, thiolation of the universally conserved methyl-uridine at position 54 stabilizes tRNAs from thermophilic bacteria and hyperthermophilic archaea and is required for growth at high temperature. The simple nonredox substitution of the C2-uridine carbonyl oxygen by sulfur is catalyzed by tRNA thiouridine synthetases called TtuA. Spectroscopic, enzymatic, and structural studies indicate that TtuA carries a catalytically essential [4Fe-4S] cluster and requires ATP for activity. A series of crystal structures shows that (i) the cluster is ligated by only three cysteines that are fully conserved, allowing the fourth unique iron to bind a small ligand, such as exogenous sulfide, and (ii) the ATP binding site, localized thanks to a protein-bound AMP molecule, a reaction product, is adjacent to the cluster. A mechanism for tRNA sulfuration is suggested, in which the unique iron of the catalytic cluster serves to bind exogenous sulfide, thus acting as a sulfur carrier.


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