Teijeiro C, Nejedlý K, Palecek E
Institute of Biophysics, Academy of Sciences of the Czech Republic, Brno.
J Biomol Struct Dyn. 1993 Oct;11(2):313-31. doi: 10.1080/07391102.1993.10508729.
We have previously shown that a DNA-modified electrode can be prepared by immersing the hanging mercury drop electrode (HMDE) in a small volume (about 5-10 microliters) of a DNA solution. Within a short period of time the DNA is irreversibly adsorbed at the electrode, resisting subsequent washing. The electrode is then transferred into a voltammetric cell filled with the background electrolyte (that does not contain any nucleic acid) in which the voltammetric measurements are performed. This procedure is called adsorptive transfer stripping voltammetry (AdTSV). In this paper AdTS cyclic voltammetry (CV) peaks of DNA were measured to report on the stability of the attachment of plasmid DNA molecules to the electrode surface. It was shown that the attachment of plasmid DNA to the electrode was, like the case of calf thymus DNA, sufficiently stable. If the DNA-modified electrode was immersed in a protein solution no significant exchange between the DNA and protein was observed. Submicrogram amounts of DNA were sufficient to attain full coverage of the electrode at relatively short waiting times and the detection limit of the denatured DNA was below 2 ng. The intensity of the AdTS CV signals of supercoiled, linearized and thermally denatured linear DNAs differed from one another. It was shown that alkaline denaturation of linear and supercoiled DNA in solution can be studied using AdTS CV technique. It was further shown that at neutral pH the linearized plasmid undergoes denaturation due to a prolonged contact with the electrode charged to potentials around -1.2 V. Such a surface denaturation has been previously observed with calf thymus DNA and synthetic double-stranded polynucleotides. Our results show that in contrast to linear DNA, supercoiled DNA was not significantly denatured as a result of its prolonged contact with the electrode charged to various potentials in the range between -0.1 to -1.5 V.
我们之前已经表明,可以通过将悬汞滴电极(HMDE)浸入少量(约5 - 10微升)DNA溶液中来制备DNA修饰电极。在短时间内,DNA不可逆地吸附在电极上,能抵抗后续的冲洗。然后将电极转移到充满背景电解质(不含任何核酸)的伏安池中进行伏安测量。这个过程称为吸附转移溶出伏安法(AdTSV)。在本文中,测量了DNA的AdTS循环伏安法(CV)峰,以报告质粒DNA分子与电极表面结合的稳定性。结果表明,质粒DNA与电极的结合,如同小牛胸腺DNA的情况一样,足够稳定。如果将DNA修饰电极浸入蛋白质溶液中,未观察到DNA与蛋白质之间有明显的交换。亚微克量的DNA足以在相对较短的等待时间内实现电极的完全覆盖,变性DNA的检测限低于2纳克。超螺旋、线性化和热变性线性DNA的AdTS CV信号强度彼此不同。结果表明,可以使用AdTS CV技术研究溶液中线性和超螺旋DNA的碱性变性。进一步表明,在中性pH下,线性化质粒由于与充电至约 - 1.2 V电位的电极长时间接触而发生变性。这种表面变性先前已在小牛胸腺DNA和合成双链多核苷酸中观察到。我们的结果表明,与线性DNA不同,超螺旋DNA在与充电至 - 0.1至 - 1.5 V范围内各种电位的电极长时间接触后,并未显著变性。