Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Central 4, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8562, Japan; Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, Tokyo 184-8588, Japan.
Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Central 4, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8562, Japan.
J Biosci Bioeng. 2014 Jan;117(1):107-12. doi: 10.1016/j.jbiosc.2013.06.019. Epub 2013 Jul 26.
We present here an alternative, force-based measurement method for the detection of intracellular cytoskeletal proteins in the live cell. High aspect ratio nanoneedles of 200 nm in diameter were functionalized with anti-tubulin antibodies and inserted, using an atomic force microscope (AFM), into live NIH3T3 cells, without affecting cell viability. Force curves were recorded during insertion and evacuation of nanoneedles from the cells, and used to analyse intracellular interactions of the nanoneedles with the microtubule cytoskeleton during evacuation from the cell. Disruption of microtubules led to a correlated time-dependent decrease in the measured intracellular binding forces, pointing to the high-sensitivity and high-specificity of this detection method. This analytical technique allows for real-time evaluation of the microtubule network in the live cell, without the need to use potentially harmful molecular markers as do conventional detection methods, and may prove beneficial in the diagnosis and investigation of cytoskeleton-associated diseases.
我们在这里提出了一种替代的、基于力的测量方法,用于检测活细胞内的细胞骨架蛋白。高纵横比的纳米针的直径为 200nm,用抗微管蛋白抗体进行功能化,并用原子力显微镜(AFM)将其插入活 NIH3T3 细胞中,而不影响细胞活力。在纳米针插入和从细胞中抽出的过程中记录力曲线,并用于分析纳米针在从细胞中抽出过程中与微管细胞骨架的细胞内相互作用。微管的破坏导致测量的细胞内结合力的相关时间依赖性下降,表明这种检测方法具有高灵敏度和高特异性。这种分析技术允许实时评估活细胞中的微管网络,而无需像传统检测方法那样使用潜在有害的分子标记物,并且可能在与细胞骨架相关疾病的诊断和研究中证明是有益的。