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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Real-time imaging of drug-membrane interactions by atomic force microscopy
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Real-time imaging of drug-membrane interactions by atomic force microscopy

机译:原子力显微镜对药物-膜相互作用的实时成像

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摘要

Understanding drug-biomembrane interactions at high resolution is a key issue in current biophysical and pharmaceutical research. Here we used real-time atomic force microscopy (AFM) imaging to visualize the interaction of the antibiotic azithromycin with lipid domains in model biomembranes. Various supported lipid bilayers were prepared by fusion of unilamellar vesicles on mica and imaged in buffer solution. Phase-separation was observed in the form of domains made of dipalmitoylphosphatidylcholine (DPPC), sphingomyelin (SM), or SM/cholesterol (SM/Chl) surrounded by a fluid matrix of dioleoylphosphatidylcholine (DOPC). Time-lapse images collected following addition of 1 mM azithromycin revealed progressive erosion and disappearance of DPPC gel domains within 60 min. We attribute this effect to the disruption of the tight molecular packing of the DPPC molecules by the drug, in agreement with earlier biophysical experiments. By contrast, SM and SM-Chl domains were not modified by azithromycin. We suggest that the higher membrane stability of SM-containing domains results from stronger intermolecular interactions between SM molecules. This work provides direct evidence that the perturbation of lipid domains by azithromycin strongly depends on the lipid nature and opens the door for developing new applications in membrane biophysics and pharmacology. (C) 2004 Elsevier B.V. All rights reserved.
机译:高分辨率了解药物-生物膜相互作用是当前生物物理和药物研究的关键问题。在这里,我们使用实时原子力显微镜(AFM)成像来可视化抗生素阿奇霉素与模型生物膜中脂质域的相互作用。通过在云母上融合单层囊泡来制备各种支持的脂质双层,并在缓冲溶液中成像。以由棕榈油酰磷脂酰胆碱(DOPC)的流体基质包围的二棕榈酰磷脂酰胆碱(DPPC),鞘磷脂(SM)或SM /胆固醇(SM / Chl)制成的结构域形式观察到相分离。添加1 mM阿奇霉素后收集的延时图像显示60分钟内进行性侵蚀和DPPC凝胶结构域消失。我们将此效应归因于与早期生物物理实验一致的药物破坏了DPPC分子的紧密分子堆积。相比之下,阿奇霉素未修饰SM和SM-Chl结构域。我们建议,包含SM的域的更高的膜稳定性是由SM分子之间更强的分子间相互作用引起的。这项工作提供了直接的证据,表明阿奇霉素对脂质结构域的扰动在很大程度上取决于脂质的性质,并为开发膜生物物理学和药理学的新应用打开了大门。 (C)2004 Elsevier B.V.保留所有权利。

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