Pietrobon D, Caplan S R
Biochemistry. 1986 Nov 18;25(23):7690-6. doi: 10.1021/bi00371a061.
The results of double-inhibitor and uncoupler-inhibitor titrations have been simulated and analyzed with a nonlinear model of delocalized protonic coupling obtained by linking two proton pump models of the kind studied by Pietrobon and Caplan [Pietrobon, D., & Caplan, S. R. (1985) Biochemistry 24, 5764-5776] through their common intermediate delta mu H. It is shown that the results predicted by a delocalized chemiosmotic model are highly dependent on the kind of relationships existing between rate of ATP synthesis, Jp, and delta mu H and rate of electron transfer, Je, and delta mu H. With nonlinear flow-force relationships all the results reported so far are not necessarily inconsistent with the delocalized chemiosmotic model provided that the relationships between rates and delta mu H satisfy the following requirements: Jp/delta mu H increases and/or Je/delta mu H decreases as (delta mu H) increases.
通过连接Pietrobon和Caplan [Pietrobon, D., & Caplan, S. R. (1985) Biochemistry 24, 5764 - 5776] 所研究的那种质子泵模型,利用一个离域质子耦合的非线性模型对双抑制剂和解偶联剂 - 抑制剂滴定结果进行了模拟和分析。结果表明,离域化学渗透模型预测的结果高度依赖于ATP合成速率Jp与ΔμH之间、电子传递速率Je与ΔμH之间存在的关系类型。对于非线性流 - 力关系,只要速率与ΔμH之间的关系满足以下要求:随着(ΔμH)增加,Jp / ΔμH增加和/或Je / ΔμH降低,那么迄今为止报道的所有结果不一定与离域化学渗透模型不一致。