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In situ single bio-molecule recognition by atomic force microscopy using functionalized tip

机译:使用功能化尖端通过原子力显微镜原位识别单个生物分子

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Atomic force microscopy is a powerful and widely used imaging technique that can visualize single molecules both in air and solution. In this paper, by functionalizing the AFM tip with antibodies, atomic force microscopy is able to identify specific types of receptors such as angiotensin II type I receptors on cells' membrane. The antibody is tethered to the AFM tip through a spacer to form a strong but flexible binding. Due to the flexibility of the spacer, the antibody bond to the AFM tip has much more chance to interact with the antigen (receptor) on cell's surface than a direct antibody coating method. Because the AFM phase image is very sensitive to the interaction force between tip and surface, the single receptors can be easily identified by passing the phase information to a band-pass filter to remove the low frequency topography signal. After adding more antibodies to the solution to block all the specific type receptor, the disappearance of the receptors in the image verify the effectiveness of this method.
机译:原子力显微镜是一种功能强大且广泛使用的成像技术,可以可视化空气和溶液中的单个分子。在本文中,通过使用抗体对AFM尖端进行功能化,原子力显微镜能够识别特定类型的受体,例如细胞膜上的I型血管紧张素II受体。抗体通过间隔子拴在AFM末端,形成牢固但灵活的结合。由于间隔物的柔性,与直接抗体包被方法相比,与AFM尖端结合的抗体与细胞表面上的抗原(受体)相互作用的机会要大得多。由于AFM相位图像对尖端和表面之间的相互作用力非常敏感,因此可以通过将相位信息传递到带通滤波器以去除低频形貌信号来轻松识别单个受体。向溶液中添加更多抗体以阻断所有特定类型的受体后,图像中受体的消失证明了该方法的有效性。

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