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Structure of the extracellular surface of the gap junction by atomic force microscopy.

机译:通过原子力显微镜观察间隙连接的细胞外表面的结构。

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摘要

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.
机译:间隙连接细胞间通道的细胞外表面用原子力显微镜在磷酸盐缓冲液中成像。吸附到云母上的完全水合的隔离间隙连接膜是不规则的薄片,宽约1-2微米,厚13.2(+/- 1.3)nm。通过增加施加到尖端的力或有时通过以中等力提高扫描速率来解剖间隙连接的顶部双层。暴露的细胞外表面显示出六边形阵列,各个通道(连接子)之间的中心距为9.4(+/- 0.9)nm。使用高质量的笔尖可以可靠且可重现地获得横向分辨率小于3.5 nm且最佳情况下约为2.5 nm的单个连接器的图像。这些膜通道从脂质膜的细胞外表面突出1.4(+/- 0.4)nm,原子力显微镜的尖端进入孔中的距离最大为0.7 nm,开口的直径为3.8(+/- 0.6)。 nm在细胞外。

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