Eddy A A, Hopkins P, Johnson E R
Department of Biochemistry and Applied Molecular Biology, University of Manchester Institute of Science and Technology, U.K.
Biochem J. 1988 Apr 1;251(1):111-4. doi: 10.1042/bj2510111.
The model envisages two components in the process, whereby Ht equivalents of co-substrate and St equivalents of substrate accumulate in the cellular compartment in time t. The first is the flow through the symport, n equivalents of co-substrate entering or leaving with each substrate equivalent. The second is the basal flow of co-substrate outside the symport. In certain specific circumstances n can be derived by plotting Ht/t against St/t. The principal requirement is that, whereas the ratio of the component flows must change in the interval t, the magnitude of the basal flow must either be zero or constant. The procedure is applied to published observations [West & Mitchell (1973) Biochem. J. 132, 587-592] on the lactose-proton symport of Escherichia coli [n = 1.075 +/- 0.064(7)] and to new observations on the isoleucine-Na+ symport of mouse ascites-tumour cells [n = 1.136 +/- 0.120(18)].
该模型设想该过程中有两个组成部分,在时间t内,共底物的Ht当量和底物的St当量在细胞区室中积累。第一个是通过同向转运体的流量,每当量底物有n当量共底物进出。第二个是同向转运体外部共底物的基础流量。在某些特定情况下,n可以通过绘制Ht/t对St/t的曲线得出。主要要求是,虽然组分流量的比例在时间间隔t内必须变化,但基础流量的大小必须为零或恒定。该程序应用于已发表的关于大肠杆菌乳糖-质子同向转运的观察结果[韦斯特和米切尔(1973年),《生物化学杂志》132卷,587 - 592页][n = 1.075±0.064(7)],以及关于小鼠腹水肿瘤细胞异亮氨酸-Na+同向转运的新观察结果[n = 1.136±0.120(18)]。