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Lengths of n-alcohols govern how Lo-Ld mixing temperatures shift in synthetic and cell-derived membranes

机译:n-醇的长度决定了合成和细胞衍生膜中Lo-Ld混合温度如何变化

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摘要

A persistent challenge in membrane biophysics has been to quantitatively predict how membrane physical properties change upon addition of new amphiphiles (e.g., lipids, alcohols, peptides, or proteins) in order to assess whether the changes are large enough to plausibly result in biological ramifications. Because of their roles as general anesthetics, n-alcohols are perhaps the best-studied amphiphiles of this class. When n-alcohols are added to model and cell membranes, changes in membrane parameters tend to be modest. One striking exception is found in the large decrease in liquid-liquid miscibility transition temperatures (Tmix) observed when short-chain n-alcohols are incorporated into giant plasma membrane vesicles (GPMVs). Coexisting liquid-ordered and liquid-disordered phases are observed at temperatures below Tmix in GPMVs as well as in giant unilamellar vesicles (GUVs) composed of ternary mixtures of a lipid with a low melting temperature, a lipid with a high melting temperature, and cholesterol. Here, we find that when GUVs of canonical ternary mixtures are formed in aqueous solutions of short-chain n-alcohols (n ≤ 10), Tmix increases relative to GUVs in water. This shift is in the opposite direction from that reported for cell-derived GPMVs. The increase in Tmix is robust across GUVs of several types of lipids, ratios of lipids, types of short-chain n-alcohols, and concentrations of n-alcohols. However, as chain lengths of n-alcohols increase, nonmonotonic shifts in Tmix are observed. Alcohols with chain lengths of 10–14 carbons decrease Tmix in ternary GUVs of dioleoyl-PC/dipalmitoyl-PC/cholesterol, whereas 16 carbons increase Tmix again. Gray et al. observed a similar influence of the length of n-alcohols on the direction of the shift in Tmix. These results are consistent with a scenario in which the relative partitioning of n-alcohols between liquid-ordered and liquid-disordered phases evolves as the chain length of the n-alcohol increases.
机译:膜生物物理学中的一项持续挑战是定量预测添加新的两亲物(例如脂质,醇,肽或蛋白质)后膜的物理性质如何变化,以评估变化是否足够大以至于可能导致生物后果。由于其作为全身麻醉剂的作用,正醇可能是此类药物中研究最好的两亲药物。当在模型和细胞膜中添加正醇时,膜参数的变化趋于适度。发现一个显着的例外是,当将短链正构醇掺入巨型质膜囊泡(GPMV)中时,液-液混溶转变温度(Tmix)大大降低。在GPMV以及低于Tmix的温度下以及在由低熔点温度的脂质,高熔点温度的脂质和胆固醇的三元混合物组成的巨型单层囊泡(GUV)中观察到了共存的有序液相和无序液相。在这里,我们发现,当在短链正构醇(n≤10)的水溶液中形成规范三元混合物的GUV时,Tmix相对于水中的GUV会增加。该变化与来自细胞的GPMV报道的方向相反。在多种类型的脂质,脂质比率,短链正构醇类型和正构醇浓度的GUV中,Tmix的增加均很强劲。然而,随着正醇链长的增加,在Tmix中观察到非单调变化。链长为10–14个碳的醇会降低三元GUV中的油酰-PC /二棕榈酰-PC /胆固醇的Tmix,而16个碳又会增加Tmix。格雷等。观察到正醇长度对Tmix转变方向的类似影响。这些结果与以下情形一致:随着n-醇链长的增加,在液体有序相和液体无序相之间n-醇的相对分配逐渐增加。

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