de Jonge N, Peckys D B, Kremers G J, Piston D W
Department of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, TN 37232-0615, USA.
Proc Natl Acad Sci U S A. 2009 Feb 17;106(7):2159-64. doi: 10.1073/pnas.0809567106. Epub 2009 Jan 21.
Single gold-tagged epidermal growth factor (EGF) molecules bound to cellular EGF receptors of fixed fibroblast cells were imaged in liquid with a scanning transmission electron microscope (STEM). The cells were placed in buffer solution in a microfluidic device with electron transparent windows inside the vacuum of the electron microscope. A spatial resolution of 4 nm and a pixel dwell time of 20 micros were obtained. The liquid layer was sufficiently thick to contain the cells with a thickness of 7 +/- 1 microm. The experimental findings are consistent with a theoretical calculation. Liquid STEM is a unique approach for imaging single molecules in whole cells with significantly improved resolution and imaging speed over existing methods.
利用扫描透射电子显微镜(STEM)在液体中对与固定成纤维细胞的细胞表皮生长因子(EGF)受体结合的单个金标记表皮生长因子分子进行成像。将细胞置于电子显微镜真空环境中带有电子透明窗口的微流控装置的缓冲溶液中。获得了4纳米的空间分辨率和20微秒的像素驻留时间。液体层足够厚,能够容纳厚度为7±1微米的细胞。实验结果与理论计算一致。液体STEM是一种独特的方法,用于对全细胞中的单个分子进行成像,与现有方法相比,其分辨率和成像速度有显著提高。