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Flat hydrogel substrate for atomic force microscopy to observe liposomes and lipid membranes

机译:扁平水凝胶基质,用于原子力显微镜观察脂质体和脂质膜

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摘要

In order to avoid denaturation of biomolecules due to strong adsorption on solid surfaces, a soft substrate has to be used for atomic force microscopy (AFM) observation. We propose a hydrophilic agarose gel surface as a soft substrate for AFM to observe liposomes and lipid membranes. Although our simple method does not require any delicate control at the molecular level, an agarose gel surface can be simply flattened to 0.3 nm in roughness using an atomically flat solid surface during gelation. The AFM images revealed that liposomes were unruptured on the gel surface at low liposome density, whereas an unruptured state was difficult to obtain on a solid surface like mica. This indicates that the weak interaction between the liposome and the soft surface inhibits the liposome from rupturing, and also that the surface rougher than the solid surface prevents lateral diffusion of the liposomes along the surface to be fused. Increasing the liposome density resulted in a lipid membrane at various thicknesses forming on the hydrogel surface by the fusion and rupture of liposomes. Using the soft substrate, it can be expected to promote investigations of structures and functions of biomolecules at the nanometer scale under physiological conditions with AFM.
机译:为了避免由于在固体表面上的强吸附而导致生物分子变性,必须使用软质基质进行原子力显微镜(AFM)观察。我们提出亲水性琼脂糖凝胶表面作为AFM的软质底物,以观察脂质体和脂质膜。尽管我们的简单方法不需要在分子水平上进行任何精细控制,但是在凝胶化过程中,使用原子上平坦的固体表面,可以将琼脂糖凝胶表面简单地平坦化为0.3 nm。 AFM图像显示脂质体在低脂质体密度下在凝胶表面未破裂,而在云母等固体表面上难以获得未破裂状态。这表明脂质体和软表面之间的弱相互作用抑制了脂质体的破裂,并且还表明,比固体表面粗糙的表面阻止了脂质体沿着要融合的表面横向扩散。通过脂质体的融合和破裂,脂质体密度的增加导致在水凝胶表面上形成各种厚度的脂质膜。使用软基质,可以预期在AFM的生理条件下促进纳米级生物分子的结构和功能的研究。

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