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由新型设计的离子载体(ETH1644)介导的锂离子跨脂质双分子层膜的选择性转运。

Selective transport of Li+ across lipid bilayer membranes mediated by an ionophore of novel design (ETH1644).

作者信息

Zeevi A, Margalit R

出版信息

J Membr Biol. 1985;86(1):61-7. doi: 10.1007/BF01871611.

Abstract

The neutral noncyclic, lithium-selective ionophore ETH1644, which is structurally different from previously available ionophores of this type, is a selective carrier of Li+ in lipid bilayer membranes of various lipid composition. The ionophore forms a 2:1 carrier/cation complex, and the rate-limiting step in the overall transport process is the diffusion of the carrier/ion complex across the membrane. The selectivity sequence for lithium vs. other ions normally found in biological systems is: Li+ (1) greater than Na+ (0.017) greater than or equal to K+ (0.017) greater than Cl- (0.001), Ca2+ and Mg2+ are impermeant. At neutral pH protons do not interfere with the Li+-carrying ability of this ionophore. On the basis of structural differences and supported by conductance data, it is argued that the improved selectivity of Li+ over the other alkali cations is due more to a decrease in the affinities of the ionophore for the latter cations that to an increase of its affinity to Li+. This ionophore can also act as a carrier of biogenic amines (catecholes, indoles and derivatives), with the structure of the permeant species and mechanism of permeation similar to that observed with the alkali cations. The selectivity sequence is: tryptamine (18.1) greater than phenylethylamine (11.6) greater than tyramine (2.4) greater than Li+ (1) greater than serotonin (0.34) greater than epinephrine (0.09) greater than dopamine (0.05) greater than norepinephrine (0.02), showing the ionophore to be more selective to Li+ than to any of the neurotransmitters studied.

摘要

中性非环状锂选择性离子载体ETH1644在结构上与此前这类可用的离子载体不同,是各种脂质成分的脂质双分子层膜中Li⁺的选择性载体。该离子载体形成2:1的载体/阳离子复合物,整个运输过程中的限速步骤是载体/离子复合物跨膜扩散。锂与生物系统中常见的其他离子的选择性顺序为:Li⁺(1)大于Na⁺(0.017)大于或等于K⁺(0.017)大于Cl⁻(0.001),Ca²⁺和Mg²⁺不可渗透。在中性pH值下,质子不会干扰该离子载体携带Li⁺的能力。基于结构差异并得到电导数据支持,有人认为Li⁺相对于其他碱金属阳离子选择性提高更多是由于离子载体对后一类阳离子的亲和力降低,而非对Li⁺的亲和力增加。这种离子载体还可作为生物胺(儿茶酚、吲哚及其衍生物)的载体,渗透物种的结构和渗透机制与碱金属阳离子类似。选择性顺序为:色胺(18.1)大于苯乙胺(11.6)大于酪胺(2.4)大于Li⁺(1)大于血清素(0.34)大于肾上腺素(0.09)大于多巴胺(0.05)大于去甲肾上腺素(0.02),表明该离子载体对Li⁺的选择性高于所研究的任何神经递质。

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