Institute of Pharmaceutical Biology and Phytochemistry, University of Münster, Münster, Germany.
Sci Rep. 2021 May 13;11(1):10214. doi: 10.1038/s41598-021-89633-2.
As a topographical technique, Atomic Force Microscopy (AFM) needs to establish direct interactions between a given sample and the measurement probe in order to create imaging information. The elucidation of internal features of organisms, tissues and cells by AFM has therefore been a challenging process in the past. To overcome this hindrance, simple and fast embedding, sectioning and dehydration techniques are presented, allowing the easy access to the internal morphology of virtually any organism, tissue or cell by AFM. The study at hand shows the applicability of the proposed protocol to exemplary biological samples, the resolution currently allowed by the approach as well as advantages and shortcomings compared to classical ultrastructural microscopic techniques like electron microscopy. The presented cheap, facile, fast and non-toxic experimental protocol might introduce AFM as a universal tool for the elucidation of internal ultrastructural detail of virtually any given organism, tissue or cell.
作为一种形貌技术,原子力显微镜(AFM)需要在创建成像信息之前在给定的样本和测量探针之间建立直接相互作用。因此,过去通过 AFM 阐明生物体、组织和细胞的内部特征一直是一个具有挑战性的过程。为了克服这一障碍,提出了简单快速的包埋、切片和脱水技术,允许通过 AFM 轻松访问几乎任何生物体、组织或细胞的内部形态。目前的研究表明,所提出的方案适用于典型的生物样本,以及该方法目前允许的分辨率,以及与电子显微镜等经典超微结构显微镜技术相比的优缺点。所提出的廉价、简便、快速且无毒的实验方案可能会将 AFM 作为阐明几乎任何给定生物体、组织或细胞内部超微结构细节的通用工具。