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Electrochemical monitoring of intracellular enzyme activity of single living mammalian cells by using a double-mediator system

机译:使用双介体系统电化学监测单个活哺乳动物细胞的细胞内酶活性

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We evaluated the intracellular NAD(P)H:quinone oxidoreductase (NQO) activity of single HeLa cells by using the menadione-ferrocyanide double-mediator system combined with scanning electrochemical microscopy (SECM). The double-mediator system was used to amplify the current response from the intracellular NQO activity and to reduce menadione-induced cell damage. The electron shuttle between the electrode and menadione was mediated by the ferrocyanide/ferricyanide redox couple. Generation of ferrocyanide was observed immediately after the addition of a lower concentration (10μM) of menadione. The ferrocyanide generation rate was constant for 120 min. At a higher menadione concentration (100μM), the ferrocyanide generation rate decreased within 30min because of the cytotoxic effect of menadione. We also investigated the relationship between intracellular reactive oxygen species or glutathione levels and exposure to different menadione concentrations to determine the optimal condition for SECM with minimal invasiveness. The present study clearly demonstrates that SECM is useful for the analysis of intracellular enzymatic activities in single cells with a double-mediator system.
机译:我们通过使用甲萘醌-亚铁氰化物双介体系统结合扫描电化学显微镜(SECM)评估了单个HeLa细胞的细胞内NAD(P)H:醌氧化还原酶(NQO)活性。使用双介体系统来放大细胞内NQO活性产生的电流响应,并减少甲萘醌诱导的细胞损伤。电极和甲萘醌之间的电子穿梭由亚铁氰化物/铁氰化物氧化还原对介导。加入较低浓度的甲萘醌后,立即观察到亚铁氰化物的生成。亚铁氰化物的生成速率在120分钟内保持恒定。在甲萘醌浓度较高(100μM)时,由于甲萘醌的细胞毒性作用,亚铁氰化物生成速率在30min内下降。我们还研究了细胞内活性氧或谷胱甘肽水平与暴露于不同甲萘醌浓度之间的关系,从而确定了具有最小侵袭性的SECM的最佳条件。本研究清楚地表明,SECM可用于使用双介体系统分析单细胞中的细胞内酶活性。

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