Vambutas V
Department of Biochemistry, Mount Sinai School of Medicine, City University of New York, New York 10029.
J Bioenerg Biomembr. 1987 Oct;19(5):525-34. doi: 10.1007/BF00770035.
The mechanism of a K+-driven Cl- accumulation against a concentration gradient was investigated by flow dialysis after addition of K+-Hepes. Non-specific chloride binding, measured in the presence of choline-Hepes, accounted for approximately 50% of the observed uptake in this system. The K+-Hepes-driven Cl- uptake was inhibited by poly-l-lysine and by two antibodies raised to the major polypeptides of the Cl(-)-efflux active particle. Poly-l-lysine had no effect on Cl- binding estimated with choline-Hepes.
在加入K+-Hepes后,通过流动透析研究了K+驱动的Cl-逆浓度梯度积累的机制。在胆碱-Hepes存在下测得的非特异性氯结合约占该系统中观察到的摄取量的50%。K+-Hepes驱动的Cl-摄取受到聚-L-赖氨酸和针对Cl(-)外流活性颗粒主要多肽产生的两种抗体的抑制。聚-L-赖氨酸对用胆碱-Hepes估计的Cl-结合没有影响。