Wain Andrew J, Zhou Feimeng
Department of Chemistry and Biochemistry, California State University-Los Angeles, Los Angeles, California 90032, USA.
Langmuir. 2008 May 6;24(9):5155-60. doi: 10.1021/la703922v. Epub 2008 Mar 21.
Scanning electrochemical microscopy (SECM) has been employed in the imaging of DNA microarrays fabricated on gold substrates using methylene blue (MB) as a redox-active intercalator and ferrocyanide as the SECM mediator in solution. MB intercalated between base pairs of immobilized ds-DNA is electrochemically reduced via electron transfer from the underlying gold substrate, and the product is reoxidized in solution by SECM tip-generated ferricyanide. The resulting feedback current allows a heterogeneous electron-transfer rate constant for the MB-intercalated DNA to be deduced. Moreover, DNA microarray spots can be imaged at a detection level of 14 fmol/spot for ds-DNA consisting of 15 base pairs. Microarrays prepared using 20 microM DNA solutions are easily visualized, and the feasibility of detecting base pair mismatches is also demonstrated.
扫描电化学显微镜(SECM)已被用于对在金基底上制备的DNA微阵列进行成像,该微阵列使用亚甲蓝(MB)作为氧化还原活性嵌入剂,并在溶液中使用亚铁氰化物作为SECM介质。嵌入固定化双链DNA碱基对之间的MB通过从下面的金基底进行电子转移而被电化学还原,产物在溶液中被SECM尖端产生的铁氰化物重新氧化。由此产生的反馈电流使得能够推导出MB嵌入DNA的异质电子转移速率常数。此外,对于由15个碱基对组成的双链DNA,DNA微阵列斑点可以在14 fmol/斑点的检测水平下成像。使用20 microM DNA溶液制备的微阵列很容易可视化,并且还证明了检测碱基对错配的可行性。