Lugmaier Robert A, Hugel Thorsten, Benoit Martin, Gaub Hermann E
Lehrstuhl für Angewandte Physik and Center for NanoScience, Ludwig-Maximilians-Universität München, Amalienstrasse 54, D-80799 München, Germany.
Ultramicroscopy. 2005 Oct;104(3-4):255-60. doi: 10.1016/j.ultramic.2005.04.008.
High-resolution optical microscopy is an essential pre-requisite for life science force microscopy, particularly for applications in cell biology and medicine. Identification and validation of cells is typically established with techniques like phase contrast microscopy or differential interference contrast microscopy. The option to select or monitor individual cells online with such light microscopy techniques while performing atomic force microscopy (AFM) measurements is therefore extremely beneficial. Here, we report two conceptually different strategies to implement these light microscopy techniques in a fully functional AFM head at the ultimate resolution of the Abbe diffraction limit.
高分辨率光学显微镜是生命科学力显微镜的一项基本前提条件,尤其适用于细胞生物学和医学领域的应用。细胞的识别和验证通常通过相差显微镜或微分干涉对比显微镜等技术来实现。因此,在进行原子力显微镜(AFM)测量时,能够使用此类光学显微镜技术在线选择或监测单个细胞,这极为有益。在此,我们报告了两种概念上不同的策略,可在阿贝衍射极限的最终分辨率下,将这些光学显微镜技术应用于功能完备的AFM探头中。