Polsky Ronen, Harper Jason C, Dirk Shawn M, Arango Dulce C, Wheeler David R, Brozik Susan M
Sandia National Laboratories, Albuquerque, New Mexico 87185, USA.
Langmuir. 2007 Jan 16;23(2):364-6. doi: 10.1021/la062916a.
A simple one-step procedure is introduced for the preparation of diazonium-enzyme adducts. The direct electrically addressable deposition of diazonium-modified enzymes is examined for electrochemical sensor applications. The deposition of diazonium-horseradish peroxidase leads to the direct electron transfer between the enzyme and electrode exhibiting a heterogeneous rate constant, ks, of 10.3 +/- 0.7 s-1 and a DeltaEp of 8 mV (v = 150 mV/s). The large ks and low DeltaEp are attributed to the intimate contact between enzyme and electrode attached by one to three phenyl molecules. Such an electrode shows high nonmediated catalytic activity toward H2O2 reduction. Future generations of arrayed electrochemical sensors and studies of direct electron transfer of enzymes can benefit from protein electrodes prepared by this method.
介绍了一种制备重氮盐-酶加合物的简单一步法。研究了重氮盐修饰酶的直接电寻址沉积在电化学传感器中的应用。重氮盐-辣根过氧化物酶的沉积导致酶与电极之间的直接电子转移,其异相速率常数ks为10.3±0.7 s-1,ΔEp为8 mV(v = 150 mV/s)。较大的ks和较低的ΔEp归因于通过一到三个苯基分子连接的酶与电极之间的紧密接触。这种电极对H2O2还原表现出高的非介导催化活性。下一代阵列式电化学传感器以及酶的直接电子转移研究可受益于用该方法制备的蛋白质电极。