Alligrant Timothy M, Dasari Radhika, Stevenson Keith J, Crooks Richard M
Department of Chemistry and Center for Nano- and Molecular Science and Technology, The University of Texas at Austin , 105 E. 24th St., Stop A5300, Austin, Texas 78712-0165 United States.
Langmuir. 2015 Oct 27;31(42):11724-33. doi: 10.1021/acs.langmuir.5b02620. Epub 2015 Oct 12.
Here we report on the effect of DNA modification on individual collisions between Pt nanoparticles (PtNPs) and ultramicroelectrode (UME) surfaces. These results extend recent reports of electrocatalytic amplification (ECA) arising from collisions between naked surfaces, and they are motivated by our interest in using ECA for low-level biosensing applications. In the present case, we studied collisions between naked PtNPs and DNA-modified Au and Hg UMEs and also collisions between DNA-modified PtNPs and naked Au and Hg UMEs. In all cases, the sensing reaction is the catalytic oxidation of N2H4. The presence of ssDNA (5-mer or 25-mer) immobilized on the UME surface has little effect on the magnitude or frequency of ECA signals, regardless of whether the electrode is Au or Hg. In contrast, when DNA is immobilized on the PtNPs and the electrodes are naked, clear trends emerge. Specifically, as the surface concentration of ssDNA on the PtNP surface increases, the magnitude and frequency of the current transients decrease. This trend is most apparent for the longer 25-mer. We interpret these results as follows. When ssDNA is immobilized at high concentration on the PtNPs, the surface sites on the NP required for electrocatalytic N2H4 oxidation are blocked. This leads to lower and fewer ECA signals. In contrast, naked PtNPs are able to transfer electrons to UMEs having sparse coatings of ssDNA.
在此,我们报告了DNA修饰对铂纳米颗粒(PtNPs)与超微电极(UME)表面之间单个碰撞的影响。这些结果扩展了近期关于裸表面之间碰撞产生的电催化放大(ECA)的报道,并且我们对将ECA用于低水平生物传感应用的兴趣推动了此项研究。在当前情况下,我们研究了裸PtNPs与DNA修饰的金和汞UME之间的碰撞,以及DNA修饰的PtNPs与裸金和汞UME之间的碰撞。在所有情况下,传感反应均为N2H4的催化氧化。无论电极是金还是汞,固定在UME表面的单链DNA(5聚体或25聚体)的存在对ECA信号的大小或频率几乎没有影响。相比之下,当DNA固定在PtNPs上且电极是裸电极时,明显的趋势就出现了。具体而言,随着PtNP表面上单链DNA的表面浓度增加,电流瞬变的大小和频率降低。这种趋势在较长的25聚体中最为明显。我们对这些结果的解释如下。当单链DNA以高浓度固定在PtNPs上时,电催化N2H4氧化所需的NP表面位点被阻断。这导致ECA信号更低且更少。相比之下,裸PtNPs能够将电子转移到具有稀疏单链DNA涂层的UME上。