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Atomic force microscope visualization of lipid bilayer degradation due to action of phospholipase A(2) and Humicola lanuginosa lipase

机译:原子力显微镜显微镜可视化由于磷脂酶A(2)和Humicola Lanuginosa脂肪酶的作用引起的脂质双层降解

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摘要

An important application of liquid cell Atomic Force Microscopy (AFM) is the study of enzyme structure and behaviour in organized molecular media that mimic in-vivo systems. In this study we demonstrate the use of AFM as a tool to study the kinetics of lipolytic enzyme reactions occurring at the surface of a supported lipid bilayer. In particular, the time course of the degradation of lipid bilayers by Phospholipase A(2) (PLA(2)) and Humicola Lanuginosa Lipase (HLL) has been investigated. Contact mode imaging allows visualization of enzyme activity on the substrate with high lateral resolution. Lipid bilayers were prepared by the Langmuir-Blodgett technique and transferred to an AFM liquid cell. Following injection of the enzyme into the liquid cell, a sequence of images was acquired at regular time intervals to allow the identification of substrate structure, preferred sites of enzyme activation, and enzyme reaction rates. (c) 2006 Elsevier B.V. All rights reserved.
机译:液体细胞原子力显微镜(AFM)的重要应用是对模拟体内系统的组织分子培养基中的酶结构和行为的研究。 在这项研究中,我们证明了AFM作为研究在负载的脂质双层表面上发生的脂解酶反应动力学的工具。 特别地,研究了通过磷脂酶A(2)(PLA(2))和HumicolaLanuginosa脂肪酶(HLL)降解脂质双层的时间过程。 接触模式成像允许具有高横向分辨率的基板上的酶活性可视化。 通过Langmuir-Blodgett技术制备脂质化双层并转移到AFM液体细胞。 在将酶注射到液体细胞之后,以规则的时间间隔获取一系列图像,以允许鉴定衬底结构,优选的酶活化位点和酶反应率。 (c)2006 Elsevier B.v.保留所有权利。

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