Laboratory of Bioengineering and Physical Science, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, DHHS, Bethesda, MD 20892, USA.
FEBS Lett. 2010 Jan 4;584(1):44-8. doi: 10.1016/j.febslet.2009.11.039.
Atomic force microscopy (AFM) is used to characterize the structure and interactions of clathrin triskelia. Time sequence images of individual, wet triskelia resting on mica surfaces clearly demonstrate conformational fluctuations of the triskelia. AFM of dried samples yields images having nanometric resolution comparable to that obtainable by electron microscopy of shadowed samples. Increased numbers of triskelion dimers and assembly intermediates, as well as structures having dimensions similar to those of clathrin cages, are observed when the triskelia were immersed in a low salt, low pH buffer. These entities have been quantified by AFM protein volume computation.
原子力显微镜(AFM)用于研究网格蛋白三腿复合物的结构和相互作用。在云母表面上,对单个湿的网格蛋白三腿复合物的时间序列成像清楚地显示了三腿复合物的构象波动。对干燥样品的 AFM 成像具有纳米级分辨率,可与电子显微镜对阴影样品的成像相媲美。当三腿复合物浸泡在低盐、低 pH 缓冲液中时,观察到更多的三腿复合物二聚体和组装中间体,以及与网格蛋白笼相似尺寸的结构。这些物质已通过 AFM 蛋白质体积计算进行了量化。