Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/34470
標題: Insight into the strong inhibitory action of salt on activity of neocarzinostatin
作者: Chin, D.H.
金德航
Li, H.H.
Sudhahar, C.G.
Tsai, P.Y.
關鍵字: Drug activity;DNA cleavage;Neocarzinostatin;Enediyne antibiotics;Antitumor;non-protein chromophore;deoxyribonucleic-acid;strand breaks;dna;damage;enediyne;activation;mechanism;cleavage;release
Project: Bioorganic & Medicinal Chemistry
期刊/報告no:: Bioorganic & Medicinal Chemistry, Volume 18, Issue 5, Page(s) 1980-1987.
摘要: 
Enediyne anticancer drugs belong to one of the most potent category in inducing DNA damage. We report 85 +/- 5% inhibition on activity of neocarzinostatin by salt. As high sodium ion concentration is a known tumor cell feature, we explored the dynamic mechanism of inhibition. Using various analytical tools, we examined parameters involved in the four consecutive steps of the drug action, namely, drug releasing from carrier protein, drug-DNA binding, drug activating, and DNA damaging. Neither protein stability, nor drug release rate, was altered by salt. The salt inhibition level was similar in between the protein-bound and unbound enediyne chromophore. Salt did not quench the thiol-induced drug activation. The inhibition was independent of DNA lesion types and irrelevant with thiol structures. Collectively, no salt interaction was found in the releasing, activating, and DNA damaging step of the drug action. However, binding with DNA decreased linearly with salt and corresponded well with the salt-induced inhibition on the drug activity. Salt interference on the affinity of DNA binding was the main and sole cause of the severe salt inhibition. The inhibition factor should be carefully considered for all agents with similar DNA binding mode. (C) 2010 Elsevier Ltd. All rights reserved.
URI: http://hdl.handle.net/11455/34470
ISSN: 0968-0896
DOI: 10.1016/j.bmc.2010.01.031
Appears in Collections:化學系所

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