用于检测遗传分子马达的环状肌动蛋白结构

M. Riegelman, J. Sellers
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引用次数: 0

摘要

描述了一种构造环形肌动蛋白丝的方法。通过微接触印刷,将硝化纤维素的圆形岛屿图案印在显微镜盖片上。然后在有图案的表面上构造一个流动池。骨骼肌球蛋白是一种非特异性附着于硝化纤维素岛的蛋白。标记的肌动蛋白丝被添加到实验中,并沿着岛屿的周长自组装,形成直径约4-6微米的环形。通过改变实验中的生化条件,结合的肌球蛋白作为连接物将组装的丝保持在这种环状结构中。荧光强度增强的环区表明“闭合环”是由末端重叠的单丝形成的。这种装配技术的适应性可以用于基于高进程肌动蛋白的运动蛋白(如肌凝蛋白V)的体外运动性分析。对影响肌凝蛋白V进程性的因素的更全面的了解可能最终有助于开发该分子在工程微和纳米流体装置中的独特功能
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Looped Actin Structures for Testing Processive Molecular Motors
A method is described for constructing looped actin filaments. Circular islands of nitrocellulose were patterned onto a microscope cover slip by micro-contact printing. A flow cell was then constructed over the patterned surface. Skeletal myosin was introduced into the assay which non-specifically attached to the nitrocellulose islands. Labeled actin filaments were added to the assay and self assembled along the perimeter of the islands to form circular loops of around 4-6 mum in diameter. By altering the biochemical conditions in the assay, the bound myosin acted as a linker to hold the assembled filament in this looped configuration. Regions of the loop with enhanced fluorescent intensity suggest "closed loops" were formed from single filaments with overlapping ends. Adaptations of this assembly technique can be used for in vitro motility assays with highly processive actin based motor proteins such as myosin V. A more complete understanding of the factors that influence the processivity of myosin V may ultimately assist in efforts to exploit the molecule's unique functionality in engineered micro- and nano-fluidic devices
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