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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Novel inner monolayer fusion assays reveal differential monolayer mixing associated with cation-dependent membrane fusion
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Novel inner monolayer fusion assays reveal differential monolayer mixing associated with cation-dependent membrane fusion

机译:新型内部单层融合测定揭示了与阳离子依赖性膜融合相关的差分单层混合

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摘要

The ability to specifically monitor the behavior of the inner monolayer lipids of membranous vesicles during the membrane fusion process is useful technically and experimentally. In this study, we have identified N-NBD-phosphatidylserine as a reducible probe particularly suitable for inner monolayer fusion assays because of its low rate of membrane translocation after reduction of the outer monolayer probes by dithionite. Data are presented on translocation as a function of temperature, vesicle size, membrane composition, and serum protein concentration. Translocation as a result of the fusion event itself was also characterized. We further show here that a second membrane-localized probe, a long wavelength carbocyanine dye referred to a diI(5)C18ds, appears to form a membrane-bound resonance energy transfer pair with N-NBD-PS, and its outer monolayer fluorescence can also be eliminated by dithionite treatment. Lipid dilution of these probes upon fusion with unlabeled membranes leads to an increase in NBD donor fluorescence, and hence is a new type of inner monolayer fusion assay. These inner monolayer probe mixing assays were compared to random lipid labeling and aqueous contents mixing assays for cation-dependent fusion of liposomes composed of phosphatidylserine and phosphatidylethanolamine. The results showed that the inner monolayer fusion assay eliminates certain artifacts and reflects fairly closely the rate of non-leaky mixing of aqueous contents due to fusion, while outer monolayer mixing always precedes mixing of aqueous contents. In fact, vesicle aggregation and outer monolayer lipid mixing were found to occur over very long periods of time without inner monolayer mixing at low cation concentrations. Externally added lysophosphatidylcholine inhibited vesicle aggregation, outer monolayer mixing and any subsequent fusion. The state of vesicle aggregation and outer monolayer exchange that occurs below the fusion threshold may represent a metastable intermediate state that may be useful for further studies of the mechanism of membrane fusion.
机译:在膜融合过程中特异性监测膜囊泡内部单层脂质行为的能力在技术上和实验上都是有用的。在这项研究中,我们已确定N-NBD-磷脂酰丝氨酸是一种可还原的探针,特别适合于内部单层融合测定,因为连二亚硫酸盐还原了外部单层探针后其膜移位率低。转运数据是温度,囊泡大小,膜组成和血清蛋白浓度的函数。融合事件本身导致的易位也得到了表征。我们在这里进一步显示,第二个膜定位探针,长波长碳菁染料称为diI(5)C18ds,似乎与N-NBD-PS形成了膜结合的共振能量转移对,其外单层荧光可以也可以通过连二亚硫酸盐处理消除。与未标记的膜融合后,这些探针的脂质稀释会导致NBD供体荧光增加,因此是一种新型的内部单层融合测定法。将这些内部单层探针混合测定与随机脂质标记和水性内容物混合测定相比较,以测定由磷脂酰丝氨酸和磷脂酰乙醇胺组成的脂质体的阳离子依赖性融合。结果表明,内部单层融合测定消除了某些伪像,并且相当紧密地反映了由于融合而引起的含水成分的非渗漏混合速率,而外部单层融合始终在含水成分的混合之前。实际上,发现在很长的时间段内发生囊聚集和外单层脂质混合,而在低阳离子浓度下没有内单层混合。外部添加的溶血磷脂酰胆碱抑制囊泡聚集,外部单层混合和任何随后的融合。在融合阈值以下发生的囊泡聚集和外部单层交换状态可能代表亚稳态中间状态,可能对进一步研究膜融合机制有用。

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