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Electron Transfer from Diamond Electrodes to Heme Peptide and Peroxidase

机译:电子从金刚石电极转移到血红素肽和过氧化物酶

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摘要

Direct electron transfer from boron-doped diamond elec-trodes to heme undecapeplide and horseredish peroxi-dase (HEP) was examined and evaluated for the applica-lion to 11202 biosensors. As-grown and oxygen plasma-treated diamond electrodes on which heme peplide is adsorbed exhibited cathodic current responses to 11202 on the basis of the direct electron transfer. In a compara-live study of carbon electrodes on which heme peplide was adsorbed, an oxygen plasma-treated diamond elec-trode exhibited responses comparable with those of an edge-oriented pyrolytic graphite (EOPG) electrode, de-spite much smaller roughness. However, electron transfer to compounds I and II of HRP from the diamond elec-trodes was much slower than that from EOPG or glassy carbon, su~esling that the ~r electrons of an sp2 carbon may play an important role in the direct electron transfer to the heme moiety of HIRP. To examine the applicability of heme peplide-modified diamond electrodes to oxidase-based biosensors, anodic current responses o(the oxygen plasma-treated diamond electrode to possible inta*rhig agents, ascorbic acid and uric acid, u~re exanined ~ compared with those of EOPG. Since the dimmd dee-trode exhibited much less sensitivity to those intusfrimg agents, the heme peplide-modified diamond dechode should be a promising 11202 biosensor for the qiplicodon to oxidase-based biosensors.
机译:研究了从硼掺杂金刚石电极到血红素十癸烯化物和马来红过氧化物酶(HEP)的直接电子转移,并评估了其在11202生物传感器中的应用。吸附了血红素肽的成年和氧等离子体处理的金刚石电极在直接电子转移的基础上对11202表现出阴极电流响应。在一个比较活的研究中,吸附有血红素肽的碳电极,经氧等离子体处理的金刚石电极显示出与边缘定向热解石墨(EOPG)电极相当的响应,尽管粗糙度要小得多。但是,从金刚石电极向HRP化合物I和II的电子转移要比从EOPG或玻璃碳转移的慢得多,这是因为sp2碳的电子可能在直接电子转移中起重要作用。 HIRP的血红素部分。为了检查血红素肽修饰的金刚石电极对基于氧化酶的生物传感器的适用性,与其他那些相比,对氧等离子体处理过的金刚石电极对可能的介导剂,抗坏血酸和尿酸的阳极电流响应进行了研究。由于昏暗的de-trode对那些instusfrimg试剂的敏感性要低得多,因此血红素肽修饰的金刚石dechode应该是一种有前途的11202生物传感器,适用于蛇纹石对基于氧化酶的生物传感器。

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