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High-resolution imaging of antibodies by tapping-mode atomic force microscopy: attractive and repulsive tip-sample interaction regimes.

机译:轻敲模式原子力显微镜对抗体的高分辨率成像:有吸引力的和排斥的尖端-样品相互作用机制。

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摘要

A force microscope operated with an amplitude modulation feedback (usually known as tapping-mode atomic force microscope) has two tip-sample interaction regimes, attractive and repulsive. We have studied the performance of those regimes to imaging single antibody molecules. The attractive interaction regime allows determination of the basic morphologies of the antibodies on the support. More importantly, this regime is able to resolve the characteristic Y-shaped domain structure of antibodies and the hinge region between domains. Imaging in the repulsive interaction regime is associated with the irreversible deformation of the molecules. This causes a significant loss in resolution and contrast. Two major physical differences distinguish the repulsive interaction regime from the attractive interaction regime: the existence of tip-sample contact and the strength of the forces involved.
机译:用振幅调制反馈操作的力显微镜(通常称为敲击模式原子力显微镜)具有两种吸头与吸头相互作用的方式。我们已经研究了那些方案对单抗体分子成像的性能。有吸引力的相互作用机制可以确定支持物上抗体的基本形态。更重要的是,该方案能够解析抗体的特征性Y形结构域结构和结构域之间的铰链区。排斥相互作用状态下的成像与分子的不可逆变形有关。这导致分辨率和对比度的重大损失。物理相互作用的两个主要区别是排斥相互作用和吸引相互作用:尖端样品接触的存在和所涉及力的强度。

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