Fachbereich Biologie/Chemie, Universität Osnabrück, Osnabrück, Germany.
Nat Protoc. 2010 Apr;5(4):670-7. doi: 10.1038/nprot.2010.19. Epub 2010 Mar 18.
In Saccharomyces cerevisiae, surface stresses acting on the cell wall or plasma membrane are detected by a group of five membrane sensors: Wsc1, Wsc2, Wsc3, Mid2 and Mtl2. Here we present protocols to measure the mechanical properties of Wsc1 sensors in their native cellular environment, using the combination of genetic manipulations with single-molecule atomic-force microscopy (AFM). We describe procedures (i) for obtaining genetically modified sensors that are fully functional and suitable for AFM analysis, i.e., elongated Wsc1 derivatives terminated with a His-tag, and (ii) for detecting and stretching single Wsc1 sensors on the surface of living S. cerevisiae cells, using AFM tips functionalized with Ni(2+)-NTA groups. These procedures are multidisciplinary to implement and need competent researchers from at least two disciplines: molecular biology and nanotechnology. For experienced researchers in biological AFM, the entire protocol can be completed in approximately 3 weeks.
在酿酒酵母中,细胞壁或质膜上的表面应力被一组五个膜传感器检测到:Wsc1、Wsc2、Wsc3、Mid2 和 Mtl2。在这里,我们介绍了使用遗传操作与单分子原子力显微镜(AFM)相结合来测量其天然细胞环境中 Wsc1 传感器机械性能的方案。我们描述了程序(i)获得完全功能且适合 AFM 分析的遗传修饰传感器,即终止于 His 标签的伸长 Wsc1 衍生物,以及(ii)使用 Ni(2+)-NTA 基团功能化的 AFM 尖端检测和拉伸活酿酒酵母细胞表面上的单个 Wsc1 传感器。这些程序具有多学科性,需要至少来自两个学科的有能力的研究人员:分子生物学和纳米技术。对于具有生物 AFM 经验的研究人员,整个方案大约可以在 3 周内完成。