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Preparation of DOPC and DPPC Supported Planar Lipid Bilayers for Atomic Force Microscopy and Atomic Force Spectroscopy

机译:DOPC和DPPC支持的平面脂质双层的制备用于原子力显微镜和原子力光谱

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摘要

Cell membranes are typically very complex, consisting of a multitude of different lipids and proteins. Supported lipid bilayers are widely used as model systems to study biological membranes. Atomic force microscopy and force spectroscopy techniques are nanoscale methods that are successfully used to study supported lipid bilayers. These methods, especially force spectroscopy, require the reliable preparation of supported lipid bilayers with extended coverage. The unreliability and a lack of a complete understanding of the vesicle fusion process though have held back progress in this promising field. We document here robust protocols for the formation of fluid phase DOPC and gel phase DPPC bilayers on mica. Insights into the most crucial experimental parameters and a comparison between DOPC and DPPC preparation are presented. Finally, we demonstrate force spectroscopy measurements on DOPC surfaces and measure rupture forces and bilayer depths that agree well with X-ray diffraction data. We also believe our approach to decomposing the force-distance curves into depth sub-components provides a more reliable method for characterising the depth of fluid phase lipid bilayers, particularly in comparison with typical image analysis approaches.
机译:细胞膜通常非常复杂,由多种不同的脂质和蛋白质组成。支持的脂质双层被广泛用作研究生物膜的模型系统。原子力显微镜和力谱技术是纳米级方法,已成功用于研究支持的脂质双层。这些方法,特别是力谱法,要求可靠地制备具有扩展覆盖范围的支持脂质双层。尽管不可靠和对囊泡融合过程缺乏完全的了解阻碍了这一有前途的领域的进展。我们在这里记录了在云母上形成液相DOPC和凝胶相DPPC双层的可靠协议。介绍了最关键的实验参数,并比较了DOPC和DPPC制备方法。最后,我们演示了在DOPC表面上的力谱测量,并测量了与X射线衍射数据非常吻合的断裂力和双层深度。我们还相信,将力-距离曲线分解为深度子成分的方法提供了一种更可靠的方法来表征液相脂质双层的深度,特别是与典型的图像分析方法相比。

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