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Quinazoline derivative from indigenous isolate, Nocardiopsis alba inhibits human telomerase enzyme
Author(s) -
Kiran K.G.,
Thandeeswaran M.,
Ayub Nawaz K.A.,
Easwaran M.,
Jayagopi K.K.,
Ebrahimi L.,
Palaniswamy M.,
Mahendran R.,
Angayarkanni J.
Publication year - 2016
Publication title -
journal of applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.889
H-Index - 156
eISSN - 1365-2672
pISSN - 1364-5072
DOI - 10.1111/jam.13281
Subject(s) - telomerase , biology , biochemistry , g quadruplex , dna , active site , docking (animal) , enzyme , stereochemistry , chemistry , gene , medicine , nursing
Aim Aim of this study was isolation and screening of various secondary metabolites produced by indigenous isolates of soil Actinomycetes for human telomerase inhibitory activity. Methods and Results Extracellular extract from culture suspension of various soil Actinomycetes species were tested for telomerase inhibitory activity. The organism which produced telomerase inhibitor was identified by 16S rRNA gene sequencing. The active fraction was purified by HPLC and analysed by GC‐MS to identify the compound. In GC‐MS analysis, the active principle was identified as 3‐[4′‐(2″‐chlorophenyl)‐2′‐thiazolyl]‐2,4‐dioxo‐1,2,3,4‐tetrahydro quinazoline. The G‐quadruplex stabilizing ability of the compound was checked by molecular docking and simulation experiments with G‐quadruplex model (PDB ID‐1L1H). The selective binding ability of the compound with G‐quadruplex over Dickerson–Drew dodecamer DNA structures showed that the compound possess high selectivity towards G‐quadruplex. Conclusions Quinazoline derivative isolated from an indigenous strain of Nocardiopsis alba inhibited telomerase. Molecular docking and simulation studies predicted that this compound is a strong stabilizer of G‐quadruplex conformation. It also showed a preferable binding to G‐quadruplex DNA over normal DNA duplex. Significance and Impact of the Study This particular compound can be suggested as a suitable compound for developing a future anticancer drug. The selectivity towards G‐quadruplex over normal DNA duplex gives a clue that it is likely to show lower cytotoxicity in normal cells.