Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093, United States.
J Am Chem Soc. 2015 Jul 22;137(28):8876-9. doi: 10.1021/jacs.5b03371. Epub 2015 Jul 8.
We demonstrate that bioorthogonal tetrazine ligations can be utilized to rapidly modify electrode surfaces, both with redox probes and enzymes. Furthermore, we show that the redox-active nature of 1,2,4,5-tetrazines can be exploited to gain electrochemical control over surface modification. To our knowledge this is the first demonstration of controlling a tetrazine ligation by changing the redox state of one of the reactants. We utilize the redox-switchable feature of tetrazine ligations for the site-selective functionalization of a 10 μm spaced interdigitated array of microelectrodes. In addition, we were able to achieve potential controlled ligation of the redox enzyme horseradish peroxidase to a macroscopic planar electrode. The rapid kinetics, bioorthogonal reactivity, and electrochemical control provided by tetrazine ligations should lead to numerous applications related to electrode functionalization.
我们证明了生物正交的四嗪连接可以被用来快速修饰电极表面,无论是与氧化还原探针还是酶一起。此外,我们还表明,1,2,4,5-四嗪的氧化还原活性可以被用来获得对表面修饰的电化学控制。据我们所知,这是首次通过改变反应物的氧化还原状态来控制四嗪连接的演示。我们利用四嗪连接的氧化还原开关特性来对 10 µm 间隔的叉指微电极阵列进行位点选择性的功能化。此外,我们还能够实现氧化还原酶辣根过氧化物酶在宏观平面电极上的电位控制连接。四嗪连接提供的快速动力学、生物正交反应性和电化学控制应该会导致与电极功能化相关的许多应用。