Afrin Rehana, Zohora Umme Salma, Uehara Hironori, Watanabe-Nakayama Takahiro, Ikai Atsushi
Biofrontier Center, Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, Japan.
J Mol Recognit. 2009 Sep-Oct;22(5):363-72. doi: 10.1002/jmr.971.
The atomic force microscope (AFM) is a versatile tool for imaging, force measurement and manipulation of proteins, DNA, and living cells basically at the single molecular level. In the cellular level manipulation, extraction, and identification of mRNA's from defined loci of a cell, insertion of plasmid DNA and pulling of membrane proteins, for example, have been reported. In this study, AFM was used to create holes at defined loci on the cell membrane for the investigation of viability of the cells after hole creation, visualization of intracellular structure through the hole and for targeted gene delivery into living cells. To create large holes with an approximate diameter of 5-10 microm, a phospholipase A(2) coated bead was added to the AFM cantilever and the bead was allowed to touch the cell surface for approximately 5-10 min. The evidence of hole creation was obtained mainly from fluorescent image of Vybrant DiO labeled cell before and after the contact with the bead and the AFM imaging of the contact area. In parallel, cells with a hole were imaged by AFM to reveal intracellular structures such as filamentous structures presumably actin fibers and mitochondria which were identified with fluorescent labeling with rhodamine 123. Targeted gene delivery was also attempted by inserting an AFM probe that was coated with the Monster Green Fluorescent Protein phMGFP Vector for transfection of the cell. Following targeted transfection, the gene expression of green fluorescent protein (GFP) was observed and confirmed by the fluorescence microscope.
原子力显微镜(AFM)是一种多功能工具,基本上可在单分子水平上对蛋白质、DNA和活细胞进行成像、力测量及操作。例如,在细胞水平上,已报道了从细胞特定位点提取和鉴定mRNA、插入质粒DNA以及牵拉膜蛋白等操作。在本研究中,使用AFM在细胞膜的特定位点制造孔洞,以研究造孔后细胞的活力、通过孔洞观察细胞内结构以及将靶向基因导入活细胞。为制造直径约5 - 10微米的大孔洞,将包被有磷脂酶A(2)的珠子添加到AFM悬臂上,并让珠子与细胞表面接触约5 - 10分钟。造孔的证据主要来自与珠子接触前后Vybrant DiO标记细胞的荧光图像以及接触区域的AFM成像。同时,用AFM对有孔细胞进行成像,以揭示细胞内结构,如推测为肌动蛋白纤维和线粒体的丝状结构,并用罗丹明123荧光标记进行鉴定。还尝试通过插入包被有绿色荧光蛋白载体phMGFP的AFM探针进行靶向基因递送,以转染细胞。靶向转染后,通过荧光显微镜观察并确认了绿色荧光蛋白(GFP)的基因表达。