氯离子和阳离子跨细胞膜共转运的生理和生物物理学。

Federation proceedings Pub Date : 1987-05-15
P K Lauf, T J McManus, M Haas, B Forbush, J Duhm, P W Flatman, M H Saier, J M Russell
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引用次数: 0

摘要

关于Na、K、Cl的耦合共输运机制仍有许多重要的问题有待解答。我们仍然不知道ATP的要求是什么。ATP是直接的能量来源吗?这样的能量来源似乎不是必需的,因为Na, K和Cl的联合跨膜化学梯度中的净自由能足以维持所观察到的高Cl(i)。是否有一种蛋白激酶介导的机制负责ATP的需求?还原Cl(i)如何刺激转运蛋白?在向外和向内的转运位点上,合作离子的动力学关系是什么?它们对称吗?鱿鱼轴突能调节细胞体积吗?如果有,Na,K,Cl转运体是否直接参与?因此,鱿鱼轴突仍然是研究类似于在各种细胞中发现的运输机制的富有成效的准备。它的大尺寸赋予了独特的实验优势,这应该有助于我们了解这种广泛分布的运输机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Physiology and biophysics of chloride and cation cotransport across cell membranes.

Many important questions remain to be answered about the mechanism that mediates coupled Na,K,Cl cotransport. We still do not know what the ATP requirement involves. Is ATP the direct energy source? Such an energy source does not seem to be necessary, inasmuch as the net free energy in the combined transmembrane chemical gradients of Na, K, and Cl is quite sufficient to maintain the observed high Cl(i). Could a protein kinase-mediated mechanism be responsible for the ATP requirement? How does reducing Cl(i) stimulate the transporter? What are the kinetic relationships for the co-ions at the outward- and inward-facing transport sites? Are they symmetrical? Can the squid axon regulate its cell volume? If so, is the Na,K,Cl transporter directly involved? Thus, the squid axon remains a fruitful preparation to study a transport mechanism similar to that found in a variety of cells. Its large size confers unique experimental advantages that should help us in our quest to understand this widely distributed transport mechanism.

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