Martínez Cristián, Kalise Dante, Barros L Felipe
Centro de Estudios Científicos (CECS) Valdivia, Chile.
Front Neuroenergetics. 2010 Sep 10;2. doi: 10.3389/fnene.2010.00027. eCollection 2010.
The production and dissipation of energy in cells is intimately linked to the movement of small molecules in and out of enzymes, channels, and transporters. An analytical model of diffusion was described previously, which was used to estimate local effects of these proteins acting as molecular sources. The present article describes a simple but more general model, which can be used to estimate the local impact of proteins acting as molecular sinks. The results show that the enzymes, transporters, and channels, whose substrates are present at relatively high concentrations like ATP, Na(+), glucose, lactate, and pyruvate, do not operate fast enough to deplete their vicinity to a meaningful extent, supporting the notion that for these molecules the cytosol is a well-mixed compartment. One specific consequence of this analysis is that the well-documented cross-talk existing between the Na(+)/K(+) ATPase and the glycolytic machinery should not be explained by putative changes in local ATP concentration. In contrast, Ca2(+) and H(+) transporters like the Na(+)/Ca2(+) exchanger NCX and the Na(+)/H(+) exchanger NHE, show experimental rates of transport that are two to three orders of magnitude faster than the rates at which the aqueous phase may possibly feed their binding sites. This paradoxical result implies that Ca2(+) and H(+) transporters do not extract their substrates directly from the bulk cytosol, but from an intermediate "harvesting" compartment located between the aqueous phase and the transport site.
细胞中能量的产生与消耗与小分子进出酶、通道和转运体的运动密切相关。之前描述了一种扩散分析模型,该模型用于估计这些作为分子源的蛋白质的局部效应。本文描述了一种简单但更通用的模型,可用于估计作为分子汇的蛋白质的局部影响。结果表明,其底物如ATP、Na⁺、葡萄糖、乳酸和丙酮酸以相对较高浓度存在的酶、转运体和通道,其运作速度不够快,无法在有意义的程度上耗尽其附近区域,这支持了对于这些分子而言,细胞质是一个充分混合的区室这一观点。该分析的一个具体结果是,Na⁺/K⁺ ATP酶与糖酵解机制之间存在的有充分记录的相互作用,不应通过局部ATP浓度的假定变化来解释。相比之下,像Na⁺/Ca²⁺交换体NCX和Na⁺/H⁺交换体NHE这样的Ca²⁺和H⁺转运体,其实验转运速率比水相可能为其结合位点提供底物的速率快两到三个数量级。这一矛盾的结果意味着Ca²⁺和H⁺转运体并非直接从大量细胞质中提取其底物,而是从位于水相和转运位点之间的中间“收集”区室中提取。