The mechanism of cytotoxicity by Naja naja atra cardiotoxin 3 is physically distant from its membrane-damaging effect
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Chen, Ku-Chung
Kao, Pei-Hsiu
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机构:Natl Sun Yat Sen Univ, Inst Biomed Sci, Kaohsiung Med Univ, Joint Res Ctr, Kaohsiung 804, Taiwan
Kao, Pei-Hsiu
Lin, Shinne-Ren
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机构:Natl Sun Yat Sen Univ, Inst Biomed Sci, Kaohsiung Med Univ, Joint Res Ctr, Kaohsiung 804, Taiwan
Lin, Shinne-Ren
Chang, Long-Sen
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Natl Sun Yat Sen Univ, Inst Biomed Sci, Kaohsiung Med Univ, Joint Res Ctr, Kaohsiung 804, TaiwanNatl Sun Yat Sen Univ, Inst Biomed Sci, Kaohsiung Med Univ, Joint Res Ctr, Kaohsiung 804, Taiwan
Chang, Long-Sen
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[1] Natl Sun Yat Sen Univ, Inst Biomed Sci, Kaohsiung Med Univ, Joint Res Ctr, Kaohsiung 804, Taiwan
[2] Kaohsiung Med Univ, Dept Med & Appl Chem, Kaohsiung 807, Taiwan
In order to dissect out whether multiple activities of cardiotoxins (CTXs) are connected, to some extent, with each other, studies on reduced and S-carboxyamidomethylated (Rcam) Naja naja atra CTX3 were carried out in the present study. Although both CTX3 and Rcam-CTX3 induced apoptotic death of PC-3 cells as evidenced by propodium iodide/annexin V double staining, degradation of procaspases and DNA fragmentation, the cytotoxicity of Rcam-CTX3 was mostly 100-fold lower than that noted with native toxin. However, Rcam-CTX3 retained approximately 38% of the membrane-damaging activity of native toxin as revealed by the decrease in calcein self-quenching from phospholipid vesicles. These results are likely to reflect that the mechanism of cytotoxicity by CTX3 is not heavily dependent on its membrane-perturbing effect, and suggest that the structural elements within CTX3 responsible for the two activities are probably separated. (c) 2007 Elsevier Ltd. All rights reserved.