Kessler M, Semenza G
J Membr Biol. 1983;76(1):27-56. doi: 10.1007/BF01871452.
At delta psi approximately equal to 0, D-glucose influx into, and efflux out of, membrane vesicles from small-intestinal brush borders are affected by trans Na+ and trans D-glucose to different extents. D-glucose influx and efflux respond to delta psi (negative at the trans side) to different extents. The small-intestinal Na+, D-glucose cotransporter is thus functionally asymmetric. This is not unexpected, in view of the structural asymmetry previously found. The characteristics of the delta psi-dependence of transinhibition by D-glucose are compatible with the mobile part of the cotransporter bearing a negative charge of at least 1 (in the substrate-free form). They are not compatible with its mobile part being electrically neutral. Pertinent equations are given in the Appendix. Partial Cleland's kinetic analysis and other criteria rule out (Iso) Ping Pong mechanisms and makes likely a Preferred Ordered mechanism, with Na+out binding to the cotransporter prior to the sugarout. A likely model is proposed aimed at providing a mechanism of flux coupling and active accumulation.
在膜电位差(Δψ)约等于0时,小肠刷状缘膜囊泡中D - 葡萄糖的流入和流出受跨膜Na⁺和跨膜D - 葡萄糖的影响程度不同。D - 葡萄糖的流入和流出对膜电位差(跨膜侧为负)的响应程度也不同。因此,小肠Na⁺ - D - 葡萄糖共转运体在功能上是不对称的。鉴于先前发现的结构不对称性,这并不意外。D - 葡萄糖反抑制的膜电位差依赖性特征与共转运体的可移动部分至少带有1个负电荷(无底物形式)相符。它们与可移动部分呈电中性不相符。附录中给出了相关方程。部分克莱兰动力学分析和其他标准排除了乒乓机制,并使优先有序机制成为可能,即胞外Na⁺在胞外糖之前与共转运体结合。提出了一个可能的模型,旨在提供通量偶联和主动积累的机制。