Department of Chemical and Engineering, Graduate School of Engineering, Kobe University, Kobe, Japan.
Nanoscale. 2015 Mar 21;7(11):4956-63. doi: 10.1039/c4nr05940a.
An atomic force microscope (AFM) can measure the adhesion force between a sample and a cantilever while simultaneously applying a rupture force during the imaging of a sample. An AFM should be useful in targeting specific proteins on a cell surface. The present study proposes the use of an AFM to measure the adhesion force between targeting receptors and their ligands, and to map the targeting receptors. In this study, Ste2p, one of the G protein-coupled receptors (GPCRs), was chosen as the target receptor. The specific force between Ste2p on a yeast cell surface and a cantilever modified with its ligand, α-factor, was measured and found to be approximately 250 pN. In addition, through continuous measuring of the cell surface, a mapping of the receptors on the cell surface could be performed, which indicated the differences in the Ste2p expression levels. Therefore, the proposed AFM system is accurate for cell diagnosis.
原子力显微镜(AFM)可以在对样品成像的同时测量样品和悬臂之间的粘附力,并施加断裂力。AFM 应该有助于针对细胞表面上的特定蛋白质。本研究提出使用 AFM 测量靶向受体与其配体之间的粘附力,并绘制靶向受体图谱。在这项研究中,选择了 G 蛋白偶联受体(GPCR)之一的 Ste2p 作为靶受体。测量了酵母细胞表面上的 Ste2p 与用其配体α因子修饰的悬臂之间的特定力,发现约为 250 pN。此外,通过对细胞表面的连续测量,可以对细胞表面上的受体进行映射,这表明 Ste2p 的表达水平存在差异。因此,所提出的 AFM 系统可准确用于细胞诊断。