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使用钴离子作为碰撞猝灭剂来探测荧光标记双层囊泡的表面电荷和稳定性。

The use of cobalt ions as a collisional quencher to probe surface charge and stability of fluorescently labeled bilayer vesicles.

作者信息

Morris S J, Bradley D, Blumenthal R

出版信息

Biochim Biophys Acta. 1985 Sep 10;818(3):365-72. doi: 10.1016/0005-2736(85)90011-2.

Abstract

Co2+ quenched the fluorescence of the lipid probes NBD-phosphatidylethanolamine (NBD-PE) and lissamine-rhodamine phosphatidylethanolamine (N-Rh-PE) incorporated into lipid vesicles, according to a collisional quenching mechanism in agreement with the Stern-Vollmer law. The quenching coefficient (Q) for NBD-PE, incorporated into uncharged phosphatidylcholine (PC) vesicles was 13.8 M-1. This value was equal to the quenching coefficient of water-soluble NBD-taurine in aqueous solution, indicating that Co2+ was readily accessible to the outer surface of PC vesicles. In phosphatidylserine-phosphatidylethanolamine (PS-PE) (1:1) vesicles, quenching was also proportional to Co2+ concentration but Q was 114 mM-1, some 8000-fold smaller. Using the Gouy-Chapman-Stern model we demonstrated that the surface density of Co2+ bound to lipid was linear with Co2+ concentration in the medium up to 7%. Co2+-associated phospholipid would in turn quench NBD-PE or N-Rh-PE by collisional quenching with lateral diffusion. We investigated the ability of Co2+ to permeate PS-PE (1:1) vesicles. Co2+ quenched fluorophores on the outer surface of large unilamellar vesicles, formed by reverse-phase evaporation. In small unilamellar vesicles Co2+ quenched probes on both outer and inner surfaces, indicating rapid permeation of the ions into the vesicles. Using stopped-flow rapid mixing, we measured the rate of influx of Co2+, and correcting for surface potential using the Gouy-Chapman-Stern model, we calculated a permeability coefficient of 10(-12) cm/s for Co2+ concentrations below 300 microM. Above this concentration, there was a very steep rise in the permeability coefficient, indicating that binding of Co2+ induces defects in the bilayer of these vesicles. This may be related to the ability of the vesicles to undergo membrane fusion. A method for calculating the membrane surface potential from Co2+ quenching data is presented.

摘要

根据符合斯特恩 - 沃尔默定律的碰撞猝灭机制,Co²⁺猝灭了掺入脂质囊泡中的脂质探针NBD - 磷脂酰乙醇胺(NBD - PE)和丽丝胺罗丹明磷脂酰乙醇胺(N - Rh - PE)的荧光。掺入不带电荷的磷脂酰胆碱(PC)囊泡中的NBD - PE的猝灭系数(Q)为13.8 M⁻¹。该值与水溶液中水溶性NBD - 牛磺酸的猝灭系数相等,表明Co²⁺易于接近PC囊泡的外表面。在磷脂酰丝氨酸 - 磷脂酰乙醇胺(PS - PE)(1:1)囊泡中,猝灭也与Co²⁺浓度成正比,但Q为114 mM⁻¹,约小8000倍。使用古依 - 查普曼 - 斯特恩模型,我们证明了与脂质结合的Co²⁺的表面密度在介质中Co²⁺浓度高达7%时与Co²⁺浓度呈线性关系。与Co²⁺相关的磷脂进而通过横向扩散的碰撞猝灭来猝灭NBD - PE或N - Rh - PE。我们研究了Co²⁺渗透PS - PE(1:1)囊泡的能力。Co²⁺猝灭了通过反相蒸发形成的大单层囊泡外表面上的荧光团。在小单层囊泡中,Co²⁺猝灭了外表面和内表面上的探针,表明离子迅速渗透到囊泡中。使用停流快速混合技术,我们测量了Co²⁺的流入速率,并使用古依 - 查普曼 - 斯特恩模型校正表面电位,我们计算出Co²⁺浓度低于300 μM时的渗透系数为10⁻¹² cm/s。高于此浓度时,渗透系数急剧上升,表明Co²⁺的结合会在这些囊泡的双层膜中诱导缺陷。这可能与囊泡进行膜融合的能力有关。本文提出了一种根据Co²⁺猝灭数据计算膜表面电位的方法。

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