Jauch P, Petersen O H, Läuger P
J Membr Biol. 1986;94(2):99-115. doi: 10.1007/BF01871191.
Electrical currents associated with sodium-coupled alanine transport in mouse pancreatic acinar cells were studied using the method of whole-cell recording with patch pipettes. Single cells or small clusters of (electrically coupled) cells were isolated by collagenase treatment. The composition of the intracellular solution could be controlled by internal perfusion of the patch pipette. In this way both inward and outward currents could be measured under "zero-trans" conditions, i.e., with finite concentrations of sodium and L-alanine on one side and zero concentrations on the other. Inward and outward currents for equal but opposite concentration gradients were found to be of similar magnitude, meaning that the cotransporter is functionally nearly symmetric. The dependence of current on the concentrations of sodium and L-alanine exhibited a Michaelis-Menten behavior. From the sodium-concentration dependence of current as well as from the reversal potential of the current in the presence of an alanine-concentration gradient, a sodium/alanine stoichiometric ratio of 1:1 can be inferred. The finding that N-methylated amino acids may substitute for L-alanine, as well as the observed pH dependence of currents indicate that the pancreatic alanine transport system is similar to (or identical with) the "A-system" which is widespread in animal cells. The transport system is tightly coupled with respect to Na+; alanine-coupled inward flow of Na+ is at least 30 times higher than uncoupled Na+ flow mediated by the cotransporter. The current-voltage characteristic of the cotransporter could be (approximately) determined from the difference of transmembrane current in the presence and in the absence of L-alanine. The sodium-concentration dependence of the current-voltage characteristic indicates that a Na+ ion approaching the binding site from the extracellular medium has to cross part of the transmembrane electric field.
利用膜片吸管全细胞记录法研究了小鼠胰腺腺泡细胞中与钠偶联丙氨酸转运相关的电流。通过胶原酶处理分离单个细胞或(电耦合的)小细胞簇。细胞内溶液的成分可通过膜片吸管的内部灌注来控制。通过这种方式,可以在“零转运”条件下测量内向和外向电流,即在一侧有有限浓度的钠和L-丙氨酸而另一侧为零浓度的情况下。发现对于相等但相反的浓度梯度,内向和外向电流大小相似,这意味着共转运体在功能上几乎是对称的。电流对钠和L-丙氨酸浓度的依赖性表现出米氏行为。从电流对钠浓度的依赖性以及在存在丙氨酸浓度梯度时电流的反转电位,可以推断出钠/丙氨酸化学计量比为1:1。N-甲基化氨基酸可替代L-丙氨酸这一发现以及观察到的电流对pH的依赖性表明,胰腺丙氨酸转运系统与动物细胞中广泛存在的“A系统”相似(或相同)。该转运系统在Na+方面紧密偶联;由丙氨酸偶联的Na+内向流动比由共转运体介导的未偶联Na+流动至少高30倍。共转运体的电流-电压特性可以(近似地)通过存在和不存在L-丙氨酸时跨膜电流的差值来确定。电流-电压特性对钠浓度的依赖性表明,从细胞外介质接近结合位点的Na+离子必须穿过部分跨膜电场。