Hochstrate P, Rüppel H
Biophys Struct Mech. 1980;6(2):125-38. doi: 10.1007/BF00535749.
By use of the microfluorimetric technique it is possible to study the diffusion of the fluorochrome di-dansylcystine (DDC) within isolated frog rod outer segments (ros) which are immobilysed in agarose gel. For this purpose, by a short hypotonic shock a leak is applied to one end of the ros. By this open end the DDC enters the rod and migrates through the whole outer segment. Following the propagation of the fluorescence boundary with time the cytoplasmatic diffusion constant can be determined if a chromatographic model is used to allow for the considerable binding of DDC to the inner membrane surface. With a binding constant K = 5 . 10(-4) cm the cytoplasmatic diffusion constant was found to be D = 1.3 . 10(-6) cm2/s whereas Dg = 2 . 10(-6 cm2/s and Dr = 3.5 . 10(-6) cm2/s were found in agarose gel or ringer solution, respectively. Using the mobility reduction factor given by D/Dr approximately equal to 0.4 to calculate the cytoplasmatic conductivity an inner resistance per length of 1.7 M omega/mu could be calculated for a frog rod which is in good agreement with corresponding data obtained from electrophysiological measurements.
通过使用显微荧光技术,可以研究荧光染料双丹磺酰胱氨酸(DDC)在固定于琼脂糖凝胶中的离体青蛙视杆外段(ROS)内的扩散情况。为此,通过短暂的低渗冲击,在视杆外段的一端造成渗漏。DDC通过这个开放端进入视杆,并在整个外段中迁移。如果使用色谱模型来考虑DDC与内膜表面的大量结合,随着荧光边界随时间的传播,就可以确定细胞质扩散常数。结合常数K = 5×10⁻⁴ cm时,发现细胞质扩散常数为D = 1.3×10⁻⁶ cm²/s,而在琼脂糖凝胶或林格氏液中分别发现Dg = 2×10⁻⁶ cm²/s和Dr = 3.5×10⁻⁶ cm²/s。使用由D/Dr给出的迁移率降低因子约等于0.4来计算细胞质电导率,对于青蛙视杆,可以计算出每长度1.7 MΩ/μm的内阻,这与从电生理测量中获得的相应数据非常吻合。