Le Grimellec C, Lesniewska E, Cachia C, Schreiber J P, de Fornel F, Goudonnet J P
Institut National de la Santé et de la Recherche Médicale U251, Faculté de Médecine Xavier-Bichat, Paris, France.
Biophys J. 1994 Jul;67(1):36-41. doi: 10.1016/S0006-3495(94)80490-4.
The membrane surface of polarized renal epithelial cells (MDCK cells) grown as a monolayer was imaged with the atomic force microscope. The surface topography of dried cells determined by this approach was consistent with electron microscopy images previously reported. Fixed and living cells in aqueous medium gave more fuzzy images, likely because of the presence of the cell glycocalix. Treatment of living cells with neuraminidase, an enzyme that partly degrades the glycocalix, allowed sub-micrometer imaging. Protruding particles, 10 to 60 nm xy size, occupy most of the membrane surface. Protease treatment markedly reduced the size of these particles, indicating that they corresponded to proteins. Tip structure effects were probably involved in the exaggerated size of imaged membrane proteins. Although further improvements in the imaging conditions, including tip sharpness, are required, atomic force microscope already offers the unique possibility to image proteins at the membrane surface of living cells.
将作为单层生长的极化肾上皮细胞(MDCK细胞)的膜表面用原子力显微镜成像。通过这种方法确定的干燥细胞的表面形貌与先前报道的电子显微镜图像一致。水介质中的固定细胞和活细胞给出的图像更模糊,可能是因为存在细胞糖萼。用神经氨酸酶(一种部分降解糖萼的酶)处理活细胞,可以进行亚微米成像。大小为xy 10至60 nm的突出颗粒占据了大部分膜表面。蛋白酶处理显著减小了这些颗粒的大小,表明它们对应于蛋白质。成像的膜蛋白尺寸夸大可能涉及针尖结构效应。尽管需要进一步改善成像条件,包括针尖锐度,但原子力显微镜已经提供了在活细胞膜表面对蛋白质进行成像的独特可能性。