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Protein nanoarray on Prolinker (TM) surface constructed by atomic force microscopy dip-pen nanolithography for analysis of protein interaction

机译:通过原子力显微镜浸蘸-笔式纳米光刻技术在Prolinker(TM)表面上构建蛋白质纳米阵列,以分析蛋白质相互作用

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摘要

Protein nanoarrays are addressable ensembles of nano-scale protein domain on solid surfaces. This method can serve as a useful platform for ultraminiaturized bioanalysis. In this study, we investigated single molecular nanopatterning and molecular interaction of proteins that were immobilized on Prolinker (TM) surface of gold-coated silicon wafer by using dip-pen nanolithography (DPN) method. Contact force and humidity were optimized at 0.01 nN and 80%, respectively. The domain features of protein nanoarrays were developed at the contact time of 5 s. The optimized conditions for the nanoarray process were applied to create protein nanoarray using integrin alpha(v)beta(3) and angiogenin. Constructed protein nanoarrays using integrin alpha(v)beta(3) have single molecular monolayer with regular domain shape (height 15 +/- 5 nm). The changed height value due to the single molecular interaction between integrin alpha(v)beta(3) and vitronectin was approximately 30 +/- 5 nm on Prolinker (TM) surface as measured with atomic force microscopy tip. Taken together, these results suggest that protein nanoarray on Prolinker (TM) surface fabricated by well-controlled DPN process can be used to analyze single molecular interaction of protein.
机译:蛋白质纳米阵列是固体表面上纳米级蛋白质结构域的可寻址集合体。该方法可作为超小型化生物分析的有用平台。在这项研究中,我们研究了通过浸涂式纳米光刻(DPN)方法固定在镀金硅片的Prolinker(TM)表面上的蛋白质的单分子纳米图案化和分子相互作用。接触力和湿度分别优化为0.01 nN和80%。蛋白质纳米阵列的域特征是在5 s的接触时间形成的。应用整合素α(v)beta(3)和血管生成素,将纳米阵列工艺的优化条件应用于创建蛋白质纳米阵列。使用整联蛋白α(v)beta(3)构建的蛋白质纳米阵列具有规则域形状(高度15 +/- 5 nm)的单分子单层。由于整合素alpha(v)beta(3)和玻连蛋白之间的单个分子相互作用而导致的高度变化值在Prolinker(TM)表面上约为30 +/- 5 nm,这是用原子力显微镜尖端测得的。综上所述,这些结果表明,通过良好控制的DPN工艺在Prolinker(TM)表面制备的蛋白质纳米阵列可用于分析蛋白质的单分子相互作用。

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