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A dual-probe fluorescence method to examine selective perturbations of membrane permeability by melittin

机译:双探针荧光法检测蜂毒肽对膜通透性的选择性扰动

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A new fluorescence method has been developed to measure simultaneously and independently the release of fluorophores from two vesicle populations. Calcein and sulforhodamine B were used as a probe couple: the leakage of these probes from vesicles can be recorded independently since they can be excited simultaneously at 510 nm, and their individual fluorescence can be isolated by measuring the fluorescence signal at 525 and 590 nm, using a T-shape fluorometer. Controls show that both probes are suitable for the leakage assay based on fluorescence self-quenching, that they do not interact physically or chemically at the concentrations used in the method, and that they leak in a similar fashion from a given vesicle type. This dual-probe technique is applied to examine the specificity of the release relative to the cholesterol content of the vesicles for melittin, a toxin. This new approach shows in a straightforward manner that melittin-induced release for a given population can be modulated by the presence of vesicles with another lipid composition and this competitive release is associated with a preferential distribution of the peptide on the targeted vesicles. (C) 1999 John Wiley & Sons, Inc. [References: 21]
机译:已经开发了一种新的荧光方法来同时独立地测量两个小泡群体中荧光团的释放。钙黄绿素和磺基若丹明B被用作探针对:由于可以在510 nm处同时激发它们,因此可以独立记录这些探针从囊泡中泄漏的情况,并且可以通过测量525和590 nm处的荧光信号来分离它们各自的荧光,使用T形荧光计。对照显示,这两种探针均适合基于荧光自猝灭的泄漏测定,在该方法使用的浓度下它们不会发生物理或化学相互作用,并且它们从给定的囊泡类型以相似的方式泄漏。这种双探针技术被用于检测相对于囊泡中毒素-蜂毒素的释放的特异性。这种新方法以直接的方式表明,给定种群的蜂毒素诱导的释放可以通过存在具有另一种脂质成分的囊泡来调节,并且这种竞争性释放与肽在靶囊泡上的优先分布有关。 (C)1999 John Wiley&Sons,Inc. [参考:21]

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