Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology, Koganei, Tokyo 184-8588, Japan.
Biosens Bioelectron. 2012 Jan 15;31(1):323-9. doi: 10.1016/j.bios.2011.10.039. Epub 2011 Oct 25.
We developed a method combining atomic force microscopy (AFM) and antibody-immobilized nanoneedles to discriminate living cells by probing intracellular cytoskeletal proteins without the need for cell labeling. The nanoneedles are ultra-thin AFM probes sharpened to 200 nm in diameter. While retracting a nanoneedle inserted into a cell, we measured the mechanical force needed to unbind the antibody-target protein complex. Using this method, the intermediate filament protein, nestin and neurofilament were successfully detected in mouse embryonic carcinoma P19 cells and rat primary hippocampal cells within a minute for a single cell and cell differentiation states could be determined. Additionally, the measured magnitude of the force detecting nestin was indicative of the malignancy of breast cancer cells. This method was shown to affect neither the doubling time of cells nor does it leave extrinsic antibodies within the examined cells, allowing to be used in subsequent analyses in their native state.
我们开发了一种结合原子力显微镜(AFM)和抗体固定纳米针的方法,通过探测细胞内细胞骨架蛋白来区分活细胞,而无需对细胞进行标记。纳米针是超锋利的 AFM 探针,直径被磨至 200nm。在缩回插入细胞的纳米针的同时,我们测量了使抗体-靶蛋白复合物分离所需的机械力。使用这种方法,我们成功地在一分钟内检测到了小鼠胚胎癌细胞 P19 细胞和大鼠原代海马细胞中的中间丝蛋白巢蛋白和神经丝,并且可以确定单个细胞和细胞分化状态。此外,检测巢蛋白所需的力的大小表明了乳腺癌细胞的恶性程度。该方法既不影响细胞的倍增时间,也不会在被检测的细胞中留下外源性抗体,允许其在自然状态下用于后续分析。