Identification of chebulinic acid as potent natural inhibitor of M. tuberculosis DNA gyrase and molecular insights into its binding mode of action
Language: 
English
Abstract: 

Drug resistant tuberculosis has threatened all the advances that have been made in TB control at the global stage in the last few decades. DNA gyrase enzymes are an excellent target for antibacterial drug discovery as they are involved in essential functions like DNA replication. Here we report, a successful application of high throughput virtual screening (HTVS) to identify an inhibitor of Mycobacterium DNA gyrase targeting the wild type and the most prevalent three double mutants of quinolone resistant DNA gyrase namely A90V+D94G, A74S+D94G and A90V+S91P. HTVS of 179.299 compounds gave five compounds with significant binding affinity. Extra presicion (XP) docking and MD simulations gave a clear view of their interaction pattern. Among them, chebulinic acid (CA), a phytocompound obtained from Terminalia chebula was the most potent inhibitor with significantly high XP docking score, -14.63, -16.46, -15.94 and -15.11 against wild type and three variants respectively. Simulation studies for a period of 16 ns indicated stable DNA gyrA-CA complex formation. This stable binding would result in inhibition of the enzyme by two mechanisms. Firstly, binding of CA causes displacement of catalytic Tyr129 away from its target DNA-phosphate molecule from 1.6 Å to 3.8-7.3 Å and secondly, by causing steric hindrance to the binding of DNA strand at DNA binding site of enzyme. The combined effect would result in loss of cleavage and religation activity of enzyme leading to bactericidal effect on tuberculosis. This phytocompound displays desirable quality for carrying forward as a lead compound for anti-tuberculosis drug development. The results presented here are solely based on computations and need to be validated experimentally in order to assert the proposed mechanism of action.

Author(s): 
Patel, Kunal
Tyagi, Chetna
Goyal, Sukriti
Jamal, Salma
Wahi, Divya
Jain, Ritu
Bharadvaja, Navneeta
Grover, Abhinav
Item Type: 
Journal Article
Publication Title: 
Computational Biology and Chemistry
Journal Abbreviation: 
Comput Biol Chem
Publication Date: 
2015-12
Publication Year: 
2015
Pages: 
37-47
Volume: 
59 Pt A
ISSN: 
1476-928X
DOI: 
10.1016/j.compbiolchem.2015.09.006
Library Catalog: 
PubMed
Extra: 
PMID: 26410242

Turabian/Chicago Citation

Kunal Patel, Chetna Tyagi, Sukriti Goyal, Salma Jamal, Divya Wahi, Ritu Jain, Navneeta Bharadvaja and Abhinav Grover. 2015-12. "Identification of chebulinic acid as potent natural inhibitor of M. tuberculosis DNA gyrase and molecular insights into its binding mode of action." Computational Biology and Chemistry 59 Pt A: 37-47. 10.1016/j.compbiolchem.2015.09.006.

Wikipedia Citation

<ref> {{Cite journal | doi = 10.1016/j.compbiolchem.2015.09.006 | issn = 1476-928X | volume = 59 Pt A | pages = 37-47 | last = Patel | first = Kunal | coauthors = Tyagi, Chetna, Goyal, Sukriti, Jamal, Salma, Wahi, Divya, Jain, Ritu, Bharadvaja, Navneeta, Grover, Abhinav | title = Identification of chebulinic acid as potent natural inhibitor of M. tuberculosis DNA gyrase and molecular insights into its binding mode of action | journal = Computational Biology and Chemistry | date = 2015-12 | pmid = | pmc = }} </ref>