磷脂酶A(2) (PLA(2))与刺棘蛇毒液中的刺棘毒素(KTX)的非共价相互作用显示出明显的协同作用,增强了它们对靶细胞的细胞毒性。

Journal of Venom Research Pub Date : 2010-09-30
Ashis K Mukherjee
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引用次数: 0

摘要

目前的研究表明,kaouthiotoxin (KTX)与来自kaouthia毒液的各自的磷脂酶A(2) (PLA(2))的非共价相互作用显示出明显的协同作用,发挥细胞毒性而不改变PLA的生化特性(2)。例如,虽然NK-PLA(2)或KTX单独不诱导明显溶血洗涤的人红细胞;而NK-PLA(2): KTX复合物的溶血效力明显更高。同样,同源的NK-PLA(2): KTX复合物与单个复合物组分相比,进一步增强了病毒感染Sf9和正常Tn昆虫细胞的选择性裂解。通过NK-PLA(2)和NK-PLA(2): KTX复合物的细胞毒性作用对完整红细胞释放的脂肪酸进行气相色谱分析表明,NK-PLA(2)或NK-PLA(2)-KTX复合物的饱和脂肪酸(SFA)和不饱和脂肪酸(UFA)的比值随着红细胞水解时间的延长而增加,表明NK-PLA(2)-KTX复合物明显更倾向于sn-2位置上有SFA的甘油磷脂。因此,可能认为KTX首先破坏靶细胞膜的稳定性,然后PLA(2)对脱位和无组织磷脂双层具有更高的酶活性,导致NK-PLA(2)-KTX复合物对细胞膜的损伤明显高于复合物的单个组分(p < 0.05)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Non-covalent interaction of phospholipase A(2) (PLA(2)) and kaouthiotoxin (KTX) from venom of Naja kaouthia exhibits marked synergism to potentiate their cytotoxicity on target cells.

Non-covalent interaction of phospholipase A(2) (PLA(2)) and kaouthiotoxin (KTX) from venom of Naja kaouthia exhibits marked synergism to potentiate their cytotoxicity on target cells.

Non-covalent interaction of phospholipase A(2) (PLA(2)) and kaouthiotoxin (KTX) from venom of Naja kaouthia exhibits marked synergism to potentiate their cytotoxicity on target cells.

Present study shows that non-covalent interaction of kaouthiotoxin (KTX) with their respective pohospholipase A(2) (PLA(2)) from the venom of N. kaouthia displayed marked synergism to exert cytotoxicity without altering the biochemical properties of PLA(2). For example, although NK-PLA(2) or KTX alone did not induce appreciable hemolysis of washed human erythrocytes; however, the hemolytic potency of NK-PLA(2): KTX complex was significantly higher. Identically, selective lysis of virus infected Sf9 and normal Tn insect cells was further enhanced by the cognate NK-PLA(2): KTX complex as compared to individual components of the complex. Gas-chromatographic analysis of fatty acids released from intact erythrocytes by cytotoxic action of individual NK-PLA(2) and NK-PLA(2): KTX complex demonstrated that ratio between saturated fatty acids (SFA) and unsaturated FA (UFA) was increasing with time of hydrolysis of RBC either in the case of NK-PLA(2) or NK-PLA(2)-KTX complex suggesting NK-PLA(2)-KTX complex apparently displayed the more preference for glycerophospholipids with SFAs on the sn-2 position. Therefore, it may be suggested that KTX first destabilize the target cell membrane followed by higher enzymatic activity of PLA(2) on dislocated and disorganized phospholipid bilayers resulting in a significantly higher (p < 0.05) membrane damage by NK-PLA(2)-KTX complex compared to individual components of the complex.

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