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Electric Field Process for the Fabrication of Higher Order Structures form Biomolecule Derivatized Nanoparticles (#1030)

机译:用于制备高阶结构的电场过程形成生物分子衍生纳米颗粒(#1030)

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An electronic microarray has been used to carry out directed self-assembly of higher order 3D structures from Biotin/Streptavidin and DNA derivatized nanoparticles. Structures with up to fifty layers of alternating biotin and streptavidin and DNA nanoparticles were fabricated using a 400 site CMOS microarray system. In this process, reconfigurable electric fields produced by the microarray device were used to rapidly transport, concentrate and accelerate the binding of 40 nanometer biotin, streptavidin and DNA derivatized nanoparticles to selected sites on the microarray. The nanoparticle layering process takes less than one minute per layer (10-20 seconds for addressing and binding nanoparticles, 40 seconds for washing). The nanoparticle addressing/binding process was monitored by changes in fluorescence intensity as each nanoparticle layer was deposited. The final multilayered 3-D structures are about two microns in thickness and 50 microns in diameter. Active structures with chemical to luminescent to fluorescent properties are now being fabricated. The use of a microelectronic array device for assisted self-assembly represents a unique example of combining "top-down" and "bottom-up" technologies into a unique nanofabrication process. Such a process will be useful for the hierarchal assembly of 3D nano, micro, and macrostructures for a variety of electronic/photonic, nanomaterials, energy and biosensor applications.
机译:已经使用电子微阵列从生物素/链霉抗生物素蛋白和DNA衍生化的纳米颗粒进行直接的自组装。使用400个位点CMOS微阵列系统制造具有最多50层交替的生物素和链霉抗生物素蛋白和DNA纳米颗粒的结构。在此过程中,通过微阵列装置产生可重新配置的电场被用来快速运输,浓缩物和加快40纳米生物素的结合,链霉亲和DNA衍生的纳米颗粒,以在微阵列上选定的位点。纳米粒子分层过程每层小于1分钟(用于寻址和结合纳米颗粒的10-20秒,洗涤40秒)。通过沉积每个纳米颗粒层的荧光强度的变化监测纳米粒子寻址/结合过程。最终多层的3-D结构厚度约为2微米,直径为50微米。现在正在制造具有化学到发光至荧光特性的活性结构。用于辅助自组装的微电子阵列装置代表了将“自上而下”和“自下而上”技术结合成独特的纳米制作过程的独特示例。这种过程对于各种电子/光子,纳米材料,能量和生物传感器应用,可用于3D纳米,微观和宏观结构的层次组装。

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