Krupka R M
93 Lonsdale Drive, London, Ontario, Canada N6G 1T4.
J Membr Biol. 1999 Nov 15;172(2):129-43. doi: 10.1007/s002329900591.
The extraordinarily low substrate specificity of P-glycoprotein conflicts with the notion that specific substrate interactions are required in the control of the reaction path in an active transport system. The difficulty is shown to be overcome by a half-coupled mechanism in which the ATP reaction is linked to carrier transformations, as in a fully coupled system, but in which the transported substrate plays a passive role. The mechanism, which requires no specific interaction with the substrate, brings about uphill transport. A half-coupled mechanism is directly supported by two observations: (i) almost completely uncoupled ATPase activity in purified P-glycoprotein, and (ii) a pattern of substrate specificity like that of passive systems, where maximum rates for different substrates vary little (unlike active systems, where maximum rates vary greatly). The mechanism accommodates other findings: partial inhibition of ATPase activity by an actively transported substrate; simultaneous binding and translocation of more than one substrate molecule; and stimulation or inhibition of the transport of one substrate molecule by another. A half-coupled system associated with an internal competitive inhibitor should behave as if tightly coupled, in agreement with the effects of the synthetic peptide, polytryptophan. The degree of coupling in the intact system is yet to be determined, however. A half-coupled ATPase mechanism could originally have evolved in a flippase, where immersion of the carrier in its substrate, the membrane lipid, precludes uncoupled ATP hydrolysis. These concepts may have wider application. An uncoupled antiport mechanism, driven by a proton gradient rather than ATP, can explain low selectivity in the SMR multidrug carriers of bacteria, and a half-coupled mechanism for the ion-driven cotransport of water (the substrate in which the carrier site is immersed) can explain a recently proposed uphill flow of water.
P-糖蛋白极低的底物特异性与主动运输系统中控制反应路径需要特定底物相互作用这一观点相矛盾。研究表明,一种半偶联机制可以克服这一难题。在这种机制中,ATP反应与载体转变相联系,如同在完全偶联系统中一样,但被运输的底物只起被动作用。该机制无需与底物进行特定相互作用就能实现上坡运输。有两项观察结果直接支持了半偶联机制:(i)纯化的P-糖蛋白中几乎完全解偶联的ATP酶活性;(ii)底物特异性模式与被动系统相似,不同底物的最大转运速率变化不大(与主动系统不同,主动系统中最大转运速率变化很大)。该机制也能解释其他发现:被主动运输的底物对ATP酶活性有部分抑制作用;能同时结合和转运多个底物分子;一种底物分子的转运可被另一种底物分子刺激或抑制。与内部竞争性抑制剂相关的半偶联系统的行为应如同紧密偶联系统,这与合成肽多色氨酸的作用效果一致。然而,完整系统中的偶联程度尚待确定。半偶联ATP酶机制最初可能是在翻转酶中进化而来的,在翻转酶中,载体沉浸在其底物(膜脂)中,可防止ATP水解解偶联。这些概念可能有更广泛的应用。由质子梯度而非ATP驱动的解偶联反向转运机制可以解释细菌SMR多药载体中的低选择性,而水(载体位点所沉浸的底物)离子驱动共转运的半偶联机制可以解释最近提出的水的上坡流动现象。