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Scanning ion conductance microscopy for imaging biological samples in liquid: A comparative study with atomic force microscopy and scanning electron microscopy

机译:扫描离子电导显微镜对液体中的生物样品成像:原子力显微镜和扫描电子显微镜的对比研究

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The present study was designed to show the applicability of scanning ion conductance microscopy (SICM) for imaging different types of biological samples. For this purpose, we first applied SICM to image collagen fibrils and showed the usefulness of the approach-retract scanning (ARS)/hopping mode for such samples with steep slopes. Comparison of SICM images with those obtained by AFM revealed that the ARS/hopping SICM mode can probe the surface topography of collagen fibrils and chromosomes at nanoscale resolution under liquid conditions. In addition, we successfully imaged cultured HeLa cells, with 15 μm in height by ARS/hopping SICM mode. Because SICM can obtain non-contact (or force-free) images, delicate cellular projections were visualized on the surface of the fixed cell. SICM imaging of live HeLa cells further demonstrated its applicability to study the morphological dynamics associated with biological processes on the time scale of minutes under liquid conditions. We further applied SICM for imaging the luminal surface of the trachea and succeeded in visualizing the surface of both ciliated and non-ciliated cells. These SICM images were comparable with those obtained by scanning electron microscopy. Although the dynamic mode of AFM provides better resolution than the ARS/hopping mode of SICM in some samples, only the latter can obtain contact-free images of samples with steep slopes, rendering it an important tool for observing live cells as well as unfixed or fixed soft samples with complicated shapes. Taken together, we demonstrate that SICM imaging, especially using an ARS/hopping mode, is a useful technique with unique capabilities for imaging the three-dimensional topography of a range of biological samples under physiologically relevant aqueous conditions.
机译:本研究旨在显示扫描离子电导显微镜(SICM)对不同类型的生物样品成像的适用性。为此,我们首先将SICM应用于胶原蛋白原纤维成像,并显示了对于这种具有陡峭斜率的样品,逼近扫描(ARS)/跳跃模式的有用性。将SICM图像与通过AFM获得的图像进行比较,发现ARS /跳跃SICM模式可以在液体条件下以纳米级分辨率探测胶原纤维和染色体的表面形貌。此外,我们通过ARS /跳跃SICM模式成功成像了高度为15μm的HeLa培养细胞。因为SICM可以获得非接触(或无力)图像,所以在固定单元的表面上可以看到精细的细胞投影。活HeLa细胞的SICM成像进一步证明了其在研究液态条件下几分钟的时间尺度上与生物过程相关的形态动力学的适用性。我们进一步将SICM应用于气管腔表面成像,并成功地可视化了纤毛和非纤毛细胞的表面。这些SICM图像与通过扫描电子显微镜获得的图像相当。尽管在某些样本中,AFM的动态模式提供的分辨率比SICM的ARS /跳变模式更好,但只有后者可以获取具有陡峭斜率的样本的非接触图像,这使其成为观察活细胞以及未固定或未固定的重要工具。固定形状复杂的软样品。综上所述,我们证明了SICM成像,特别是使用ARS /跳频模式的成像,是一种有用的技术,具有独特的功能,可以在生理相关的水性条件下对一系列生物样品的三维形貌进行成像。

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