ca和h通道和传送器上的收获天线的一般要求。

Frontiers in neuroenergetics Pub Date : 2010-09-10 eCollection Date: 2010-01-01 DOI:10.3389/fnene.2010.00027
Cristián Martínez, Dante Kalise, L Felipe Barros
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引用次数: 24

摘要

细胞中能量的产生和耗散与小分子进出酶、通道和转运体的运动密切相关。先前描述了扩散的分析模型,该模型用于估计这些蛋白质作为分子源的局部效应。本文描述了一个简单但更一般的模型,它可以用来估计作为分子汇的蛋白质的局部影响。结果表明,酶、转运体和通道的底物浓度相对较高,如ATP、Na(+)、葡萄糖、乳酸和丙酮酸,它们的运作速度不够快,不足以在有意义的程度上耗尽它们附近的物质,这支持了细胞质是一个混合良好的隔间的概念。这一分析的一个具体结果是,Na(+)/K(+) ATP酶和糖酵解机制之间存在的充分记录的串扰不应该用假定的局部ATP浓度的变化来解释。相比之下,Ca2(+)和H(+)转运体,如Na(+)/Ca2(+)交换剂NCX和Na(+)/H(+)交换剂NHE,显示出的实验运输速率比水相可能提供其结合位点的速率快两到三个数量级。这个矛盾的结果意味着Ca2(+)和H(+)转运体不直接从散装细胞质中提取底物,而是从位于水相和运输位点之间的中间“收获”室中提取底物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

General requirement for harvesting antennae at ca and h channels and transporters.

General requirement for harvesting antennae at ca and h channels and transporters.

General requirement for harvesting antennae at ca and h channels and transporters.

General requirement for harvesting antennae at ca and h channels and transporters.

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.

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