Takahashi Hirohide, Hizume Kohji, Kumeta Masahiro, H Yoshimura Shige, Takeyasu Kunio
Laboratory of Plasma Membrane and Nuclear Signaling, Kyoto University Graduate School of Biostudies, Japan.
Arch Histol Cytol. 2009;72(4-5):217-25. doi: 10.1679/aohc.72.217.
Atomic force microscopy (AFM) has been a useful technique to visualize cellular and molecular structures at single-molecule resolution. The combination of imaging and force modes has also allowed the characterization of physical properties of biological macromolecules in relation to their structures. Furthermore, recognition imaging, which is obtained under the TREC(TM) (Topography and RECognition) mode of AFM, can map a specific protein of interest within an AFM image. In this study, we first demonstrated structural properties of purified α Actinin-4 by conventional AFM. Since this molecule is an actin binding protein that cross-bridges actin filaments and anchors it to integrin via tailin-vinculin-α actinin adaptor-interaction, we investigated their structural properties using the recognition mode of AFM. For this purpose, we attached an anti-α Actinin-4 monoclonal antibody to the AFM cantilever and performed recognition imaging against α Actinin-4. We finally succeeded in mapping the epitopic region within the α Actinin-4 molecule. Thus, recognition imaging using an antibody coupled AFM cantilever will be useful for single-molecule anatomy of biological macromolecules and structures.
原子力显微镜(AFM)是一种在单分子分辨率下可视化细胞和分子结构的有用技术。成像模式和力模式的结合还能够表征生物大分子与其结构相关的物理性质。此外,在AFM的TREC(形貌与识别)模式下获得的识别成像,可以在AFM图像中绘制出感兴趣的特定蛋白质。在本研究中,我们首先通过传统AFM展示了纯化的α辅肌动蛋白-4的结构特性。由于该分子是一种肌动蛋白结合蛋白,通过尾蛋白-纽蛋白-α辅肌动蛋白衔接子相互作用使肌动蛋白丝交叉连接并将其锚定到整合素上,我们使用AFM的识别模式研究了它们的结构特性。为此,我们将抗α辅肌动蛋白-4单克隆抗体连接到AFM悬臂上,并对α辅肌动蛋白-4进行识别成像。我们最终成功绘制出α辅肌动蛋白-4分子内的表位区域。因此,使用抗体偶联AFM悬臂的识别成像将有助于生物大分子和结构的单分子解剖学研究。