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Biomimetic nanolithography and its application for biosensor chipfabrication

机译:仿生纳米光刻及其对生物传感器芯片特征的应用

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Various nano-structures and complex patterns have been fabricated by top-down or bottom-up approaches, which have own strength and weakness. Here we combined the top-down and the bottom-up fabrications to take advantages on both strengths. We demonstrated that two different ways of the top-down/bottom-up combination could be very effective for the future nano-fabrications. One way is to assemble nanometer-sized building blocks into the device configurations such as electronics and sensor. Our strategy is to use those functionalized peptide nanowires, which can recognize and selectively bind a well-defined region on antigen-patterned substrates, as building blocks to assemble nanoscale architectures at uniquely defined positions, patterned by AFM-based nanolithography. The second method of the top-down/bottom-up combination is to pattern mineralization peptides with nanolithography and grow metals along the peptide lines. For example, when an Au-mineralizing peptide was written in the line-array, the biomineralization yielded monodisperse Au-NPs along the peptide lines. We were also succeeded to grow and pattern semiconductors at room temperature as precursors were patterned with dip-pen nanolithography. This crystallization was induced by energy gain from the shape change caused by DPN. Then, hydrophobic-hydrophilic pattern that mimics protein-binding sites in nature could be patterned by DPN and this pattern geometry can induce the attachment-detachment switching of proteins. At last, the electronic pathogen sensor chips will be introduced as another example for the DPN application. Here the DPN was applied to attach single cell at a time on transducer surface, which unambiguously determined the single cell detection limit of the sensors.
机译:通过自上而下或自下而上的方法制造了各种纳米结构和复杂的图案,其具有自身的强度和弱点。在这里,我们将自上而下和自下而上的制造,以对两个优点进行优势。我们证明,自上而下/自下而上组合的两种不同的方式对于未来的纳米制作来说可能非常有效。一种方式是将纳米大小的构建块组装到诸如电子和传感器的器件配置中。我们的策略是使用这些官能化肽纳米线,其可以识别和选择性地将抗原图案的基板上的明确定义的区域结合,作为在由AFM的纳米型纳米线图案化的唯一限定位置以唯一限定的位置组装纳米级架构的结构块。自上而下/自下而上组合的第二种方法是将矿化肽与纳米光刻进行塑化,沿肽系生长金属。例如,当用线阵列写入Au-in-in-in-in-in-in-in-inemeration肽时,生物矿化沿肽线产生单分散的Au-nps。我们也成功地在室温下成长和模式半导体,因为前体用倾倾纳米光刻图案化。通过由DPN引起的形状变化的能量增益诱导该结晶。然后,可以通过DPN图案化模拟蛋白质结合位点的疏水性 - 亲水模式,并且该图案几何形状可以诱导蛋白质的附着 - 脱离切换。最后,将引入电子病原体传感器芯片作为DPN应用的另一个例子。这里,在换能器表面上施加DPN以连接单个电池,该换能器表面毫不含糊地确定传感器的单个电池检测极限。

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