Zhou Junfeng, Campbell Charles, Heller Adam, Bard Allen J
Department of Chemistry and Biochemistry, University of Texas at Austin, 78712, USA.
Anal Chem. 2002 Aug 15;74(16):4007-10. doi: 10.1021/ac015721a.
Scanning electrochemical microscopy (SECM) was used to study horseradish peroxidase (HRP) immobilized with copolymer on insulating substrates (glass slide or polycarbonate membrane filter). Two methods were used to immobilize HRP: In the first, HRP was coimmobilized by cross-linking on a glass slide with a copolymer swelled in water to form a hydrogel; in the second, the same copolymer and avidin were coimmobilized on the glass slide and biotin-labeled HRP was conjugated to the avidin of the film. SECM was then used to detect the presence of the bound enzyme by observing the feedback current in a solution of benzoquinone and hydrogen peroxide, when hydroquinone was generated at the tip. A detection limit less than 7 x 10(5) HRP molecules within a approximately 7-microm-diameter area was demonstrated.
扫描电化学显微镜(SECM)用于研究辣根过氧化物酶(HRP)与共聚物一起固定在绝缘基底(载玻片或聚碳酸酯膜滤器)上的情况。采用了两种方法固定HRP:第一种方法是,将在水中溶胀形成水凝胶的共聚物在载玻片上通过交联共固定HRP;第二种方法是,将相同的共聚物和抗生物素蛋白共固定在载玻片上,然后将生物素标记的HRP与膜上的抗生物素蛋白结合。当在尖端产生对苯二酚时,通过观察苯醌和过氧化氢溶液中的反馈电流,利用SECM检测结合酶的存在。结果表明,在直径约7微米的区域内,检测限小于7×10⁵个HRP分子。