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Membrane potential-driven translocation of a lipid-conjugated rhodamine

机译:膜结合的若丹明的膜电位驱动易位

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摘要

The present study demonstrates that the permanently positively charged, lipid-conjugated rhodamine, R18, can be transported from the outer to the inner leaflet of lipid bilayers in response of a transmembrane potential (negative inside). This conclusion was based on the following observations. (i) A fast decrease of the R18 fluorescence, when present at self-quenching concentrations in DOPC large unilamellar vesicles, was revealed upon induction of a valinomycin-induced K+-diffusion potential. (ii) Iodide quenching experiments demonstrated that R18 was no longer accessible to externally added aqueous quencher after application of a transmembrane potential. (iii) 2H-NMR measurements, using DOPC, specifically deuterated at the α-position of the phosphocholine head group, revealed a massive transbilayer movement of R18 upon induction of a membrane potential. The extent of the fluorescence changes were found to be dependent on the magnitude of the applied transmembrane potential, which opens possibilities for novel applications of R18 as an internal lipid-conjugated membrane potential probe.
机译:本研究表明,在跨膜电位(内部为负)的响应下,永久性带正电荷的脂质结合的若丹明R18可从脂质双层的外部小叶向内部转移。该结论基于以下观察。 (i)在诱导瓦里霉素诱导的K +扩散潜能时,发现在DOPC大单层囊泡中以自猝灭浓度存在时,R18荧光快速降低。 (ii)碘化物淬灭实验表明,在施加跨膜电位后,外部添加的水性淬灭剂不再可接近R18。 (iii)使用DOPC的2 H-NMR测量,特别是在磷酸胆碱头部基团的α-位置氘化,显示出在诱导膜电位时R 18的大规模跨双层运动。发现荧光变化的程度取决于所施加的跨膜电位的大小,这为R18作为内部脂质缀合的膜电位探针的新应用打开了可能性。

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