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Atomic Force Microscopy of Red-Light Photoreceptors Using PeakForce Quantitative Nanomechanical Property Mapping

机译:使用PeakForce定量纳米力学性质映射的红光感光体原子力显微镜

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摘要

Atomic force microscopy (AFM) uses a pyramidal tip attached to a cantilever to probe the force response of a surface. The deflections of the tip can be measured to ~10 pN by a laser and sectored detector, which can be converted to image topography. Amplitude modulation or “tapping mode” AFM involves the probe making intermittent contact with the surface while oscillating at its resonant frequency to produce an image. Used in conjunction with a fluid cell, tapping-mode AFM enables the imaging of biological macromolecules such as proteins in physiologically relevant conditions. Tapping-mode AFM requires manual tuning of the probe and frequent adjustments of a multitude of scanning parameters which can be challenging for inexperienced users. To obtain high-quality images, these adjustments are the most time consuming.PeakForce Quantitative Nanomechanical Property Mapping (PF-QNM) produces an image by measuring a force response curve for every point of contact with the sample. With ScanAsyst software, PF-QNM can be automated. This software adjusts the set-point, drive frequency, scan rate, gains, and other important scanning parameters automatically for a given sample. Not only does this process protect both fragile probes and samples, it significantly reduces the time required to obtain high resolution images. PF-QNM is compatible for AFM imaging in fluid; therefore, it has extensive application for imaging biologically relevant materials.The method presented in this paper describes the application of PF-QNM to obtain images of a bacterial red-light photoreceptor, RpBphP3 (P3), from photosynthetic R. palustris in its light-adapted state. Using this method, individual protein dimers of P3 and aggregates of dimers have been observed on a mica surface in the presence of an imaging buffer. With appropriate adjustments to surface and/or solution concentration, this method may be generally applied to other biologically relevant macromolecules and soft materials.
机译:原子力显微镜(AFM)使用附着在悬臂上的锥形尖端来探测表面的力响应。可以通过激光和扇形检测器将尖端的偏转测量为〜10 pN,然后可以将其转换为图像形貌。调幅或“攻丝模式” AFM涉及探针与表面间歇接触,同时以其共振频率振荡以产生图像。轻敲模式原子力显微镜与流体细胞配合使用,可以在生理相关条件下对生物大分子(例如蛋白质)成像。攻丝模式AFM需要手动调整探头并经常调整众多扫描参数,这对于没有经验的用户而言可能是一个挑战。要获得高质量的图像,这些调整最耗时。PeakForce纳米力学定量定量映射(PF-QNM)通过测量与样品接触的每个点的力响应曲线来生成图像。使用ScanAsyst软件,可以自动执行PF-QNM。该软件可以自动调整给定样本的设定点,驱动频率,扫描速率,增益和其他重要的扫描参数。此过程不仅可以保护易碎的探头和样品,还可以大大减少获取高分辨率图像所需的时间。 PF-QNM与流体中的AFM成像兼容;因此,它在生物学相关材料的成像中具有广泛的应用。本文介绍的方法描述了PF-QNM在光合作用的拟南芥中获得细菌红光感光体RpBphP3(P3)图像的应用。适应状态。使用这种方法,在成像缓冲液的存在下,在云母表面观察到了P3的单个蛋白质二聚体和二聚体聚集体。通过适当调整表面和/或溶液的浓度,该方法通常可应用于其他生物学相关的大分子和软材料。

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