Applications of scanning probe microscopy in neuroscience research

D. McRae, Z. Leonenko
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Abstract

Scanning probe microscopy techniques allow for label-free high-resolution imaging of cells, tissues, and biomolecules in physiologically relevant conditions. These techniques include atomic force microscopy (AFM), atomic force spectroscopy, and Kelvin probe force microscopy, which enable high resolution imaging, nanomanipulation and measurement of the mechanoelastic properties of neuronal cells, as well as scanning ion conductance microscopy, which combines electrophysiology and imaging in living cells. The combination of scanning probe techniques with optical spectroscopy, such as with AFM-IR and tip-enhanced Raman spectroscopy, allows for the measurement of topographical maps along with chemical identity, enabled by spectroscopy. In this work, we review applications of these techniques to neuroscience research, where they have been used to study the morphology and mechanoelastic properties of neuronal cells and brain tissues, and to study changes in these as a result of chemical or physical stimuli. Cellular membrane models are widely used to investigate the interaction of the neuronal cell membrane with proteins associated with various neurological disorders, where scanning probe microscopy and associated techniques provide significant improvement in the understanding of these processes on a cellular and molecular level.
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扫描探针显微镜在神经科学研究中的应用
扫描探针显微镜技术可在生理相关条件下对细胞、组织和生物分子进行无标记高分辨率成像。这些技术包括原子力显微镜(AFM)、原子力光谱仪和开尔文探针力显微镜,可对神经细胞的机械弹性特性进行高分辨率成像、纳米操纵和测量,以及扫描离子电导显微镜,它将电生理学与活细胞成像相结合。扫描探针技术与光学光谱学(如原子力显微镜-红外光谱仪和针尖增强拉曼光谱)相结合,可通过光谱学测量地形图和化学特性。在这项工作中,我们将回顾这些技术在神经科学研究中的应用,这些技术已被用于研究神经细胞和脑组织的形态和机械弹性特性,以及研究这些特性在化学或物理刺激下的变化。细胞膜模型被广泛用于研究神经元细胞膜与与各种神经系统疾病相关的蛋白质之间的相互作用,扫描探针显微镜和相关技术大大提高了对这些过程在细胞和分子水平上的理解。
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