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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Blistering of supported lipid membranes induced by Phospholipase D, as observed by real-time atomic force microscopy
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Blistering of supported lipid membranes induced by Phospholipase D, as observed by real-time atomic force microscopy

机译:实时原子力显微镜观察到的磷脂酶D诱导的支持脂质膜起泡

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Phospholipase D from Streptomyces chromofuscus (PLDSc) is a soluble enzyme known to be activated by the phosphatidic acid (PA)-calcium complexes. Despite the vast body of literature that has accumulated on this enzyme, the exact mechanism of activation remains poorly understood. In this work. we report the first observation of PLDSc activity in real time and at nanometer resolution using atomic force microscopy (AFM). AFM images of continuous and patchy dipalmitoylphosphatidylcholine (DPPC) bilayers were recorded, prior and after incubation with PLDSc. For continuous bilayers, the enzyme induced important morphological alterations; holes corresponding to the bilayer thickness were created, while an additional elevated phase, about 2.5 nm high, was observed. This bilayer blistering is believed to be due to the production of the negatively charged lipid PA that would cause localized repulsions between the bilayer and the underlying mica surface. By contrast, these elevated domains were not seen on patchy bilayers incubated with the enzyme. Instead, the shapes of DPPC patches were strongly deformed by enzyme activity and evolved into melted morphologies. These results point to the importance of lipid packing on PLD activity and illustrate the potential of AFM for visualizing remodeling enzymatic activities. (c) 2007 Elsevier B.V. All rights reserved.
机译:染色体链霉菌(PLDSc)的磷脂酶D是一种可溶性酶,已知会被磷脂酸(PA)-钙复合物激活。尽管有关这种酶的文献很多,但对激活的确切机制仍知之甚少。在这项工作中。我们报告了使用原子力显微镜(AFM)实时且以纳米分辨率对PLDSc活性的首次观察。在与PLDSc孵育之前和之后,记录连续和不连续的二棕榈酰磷脂酰胆碱(DPPC)双层的AFM图像。对于连续的双层,该酶诱导重要的形态学改变。产生了与双层厚度相对应的空穴,同时观察到另外的升高的相,约2.5nm高。该双层起泡被认为是由于带负电荷的脂质PA的产生,其将导致双层和下面的云母表面之间的局部排斥。相反,这些升高的结构域在用该酶孵育的不规则双层上看不到。取而代之的是,DPPC斑块的形状因酶的活性而强烈变形,并演变成融化的形态。这些结果指出脂质包装对PLD活性的重要性,并说明了AFM在可视化重塑酶活性方面的潜力。 (c)2007 Elsevier B.V.保留所有权利。

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