Hoh J H, Sosinsky G E, Revel J P, Hansma P K
Department of Physics, University of California, Santa Barbara 93106.
Biophys J. 1993 Jul;65(1):149-63. doi: 10.1016/S0006-3495(93)81074-9.
The extracellular surface of the gap junction cell-to-cell channels was imaged in phosphate-buffered saline with an atomic force microscope. The fully hydrated isolated gap junction membranes adsorbed to mica were irregular sheets approximately 1-2 microns across and 13.2 (+/- 1.3) nm thick. The top bilayer of the gap junction was dissected by increasing the force applied to the tip or sometimes by increasing the scan rate at moderate forces. The exposed extracellular surface revealed a hexagonal array with a center-to-center spacing of 9.4 (+/- 0.9) nm between individual channels (connexons). Images of individual connexons with a lateral resolution of < 3.5 nm, and in the best case approximately 2.5 nm, were reliably and reproducibly obtained with high-quality tips. These membrane channels protruded 1.4 (+/- 0.4) nm from the extracellular surface of the lipid membrane, and the atomic force microscope tip reached up to 0.7 nm into the pore, which opened up to a diameter of 3.8 (+/- 0.6) nm on the extracellular side.
用原子力显微镜在磷酸盐缓冲盐溶液中对间隙连接细胞间通道的细胞外表面进行成像。吸附在云母上的完全水合的分离间隙连接膜是不规则的薄片,直径约1 - 2微米,厚度为13.2(±1.3)纳米。通过增加施加在探针上的力,或者有时通过在中等力的情况下增加扫描速率,来剖析间隙连接的顶层双层膜。暴露的细胞外表面显示出一个六边形阵列,单个通道(连接子)之间的中心间距为9.4(±0.9)纳米。使用高质量探针能够可靠且可重复地获得横向分辨率小于3.5纳米、最佳情况下约为2.5纳米的单个连接子图像。这些膜通道从脂质膜的细胞外表面突出1.4(±0.4)纳米,原子力显微镜探针深入孔中达0.7纳米,该孔在细胞外侧开口直径为3.8(±0.6)纳米。