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DNA杂交的电频率依赖性表征

Electrical frequency dependent characterization of DNA hybridization.

作者信息

Gheorghe Marin, Guiseppi-Elie Anthony

机构信息

Department of Chemical Engineering and Center for Bioelectronics, Biosensors and Biochips, Virginia Commonwealth University, Richmond, VA 23284-3028, USA.

出版信息

Biosens Bioelectron. 2003 Nov 15;19(2):95-102. doi: 10.1016/s0956-5663(03)00179-9.

Abstract

The hybridization of oligomeric DNA was investigated using the frequency dependent techniques of electrochemical impedance spectroscopy (EIS) and quartz crystal microgravimetry (QCM). Synthetic 5'-amino terminated single stranded oligonucleotides (ssDNA) were attached to the exposed glass surface between the digits of microlithographically fabricated interdigitated microsensor electrodes using 3-glycidoxypropyl-trimethoxysilane. Similar ssDNA immobilization was achieved to the surface of the gold driving electrodes of AT-cut quartz QCM crystals using 3-mercaptopropyl-trimethoxysilane. Significant changes in electrochemical impedance values (both real and imaginary components) (11% increase in impedance modulus at 120 Hz) and resonant frequency values (0.004% decrease) were detected as a consequence of hybridization of the bound ssDNA upon exposure to its complement under hybridization conditions. Non-complementary (random) sequence sowed a modest decrease in impedance and a non-detectable change in resonant frequency. The possibility to detect the binding state of DNA in the vicinity of an electrode, without a direct connection between the measurement electrode and the DNA, has been demonstrated. The potential for development of label-free, low density DNA microarrays is demonstrated and is being pursued.

摘要

使用电化学阻抗谱(EIS)和石英晶体微天平(QCM)的频率相关技术研究了寡聚DNA的杂交。使用3-缩水甘油氧基丙基三甲氧基硅烷,将合成的5'-氨基末端单链寡核苷酸(ssDNA)连接到微光刻制造的叉指式微传感器电极指状结构之间暴露的玻璃表面。使用3-巯基丙基三甲氧基硅烷,在AT切割石英QCM晶体的金驱动电极表面实现了类似的ssDNA固定。在杂交条件下,当结合的ssDNA与它的互补链杂交时,检测到电化学阻抗值(实部和虚部)有显著变化(在120Hz时阻抗模量增加11%)和谐振频率值有变化(降低0.004%)。非互补(随机)序列显示阻抗有适度降低,谐振频率有不可检测的变化。已经证明了在不使测量电极与DNA直接连接的情况下检测电极附近DNA结合状态的可能性。展示了开发无标记、低密度DNA微阵列的潜力,并且正在进行相关研究。

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