Department of Bioengineering, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.
Biosens Bioelectron. 2010 Dec 15;26(4):1449-54. doi: 10.1016/j.bios.2010.07.079. Epub 2010 Jul 30.
We developed a novel nanobiosensor for monitoring mRNA expression in a single living cell by using an atomic force microscope (AFM) equipped with a nanoprobe. The nanoprobe was constructed by immobilizing a biotin-modified molecular beacon onto an ultrathin needle (nanoneedle) via neutravidin. In order to evaluate the effectiveness of the nanoprobe, we selected glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA as the target. A single HeLa cell contained approximately 1000 copies of GAPDH mRNA. The nanoprobe was directly inserted into living HeLa cells, and it reacted with the intrinsic target mRNA within the cells. The nanoprobe could be renatured by pulling it out of the cells. Further, we successfully used the nanoprobe for continuous detection of GAPDH mRNA in multiple cells, i.e., the nanoprobe was highly specific and sensitive for the detection of intrinsic mRNA in single living cells. mRNAs are thought to be highly condensed because of the large number of organelles and complexes present in cells and the limited space available for distribution. Therefore, direct analysis of intrinsic mRNAs in living cells would be advantageous, and our novel nanoprobe is highly suitable for monitoring the RNAs in living cells.
我们开发了一种新型的纳米生物传感器,用于通过配备纳米探针的原子力显微镜(AFM)监测单个活细胞中的 mRNA 表达。纳米探针通过中性亲和素将生物素修饰的分子信标固定在超微针(纳米针)上构建而成。为了评估纳米探针的有效性,我们选择甘油醛-3-磷酸脱氢酶(GAPDH)mRNA 作为靶标。单个 HeLa 细胞中大约含有 1000 个 GAPDH mRNA 拷贝。纳米探针直接插入活的 HeLa 细胞中,并与细胞内的内在靶标 mRNA 反应。通过将纳米探针从细胞中拔出,可以使其重新复性。此外,我们成功地使用纳米探针对多个细胞中的 GAPDH mRNA 进行了连续检测,即纳米探针对单个活细胞中内在 mRNA 的检测具有高度特异性和敏感性。由于细胞内存在大量的细胞器和复合物,以及有限的分布空间,mRNA 被认为是高度浓缩的。因此,直接分析活细胞内的内在 mRNA 将是有利的,我们的新型纳米探针非常适合监测活细胞中的 RNA。