首页> 外文会议>Annual International Conference on Micro Electro Mechanical Systems >Shape control of filamentous motor proteins for bio-nano driving units
【24h】

Shape control of filamentous motor proteins for bio-nano driving units

机译:生物纳米驱动装置丝状电机蛋白的形状控制

获取原文

摘要

This paper describes a technique for controlling the shape of filamentous motor proteins for the bio-nano driving units in MEMS devices. In this experiment, we have used Actin, a protein to construct cytoskeleton. Actin monomers (G-actin) polymerize in high salt condition and form filaments (F-actin); the filaments move when they bind with the motor protein (Myosin) in ATP (adenosine tri-phosphate) solution. Fascin, a putative bundling protein, tightly bundles several F-actins together to form tight bundles of actin [1]. When G-actin and the fascin solution was confined and polymerized in the polydimethylsiloxane (PDMS) or parylene micro chambers, we found that the polymerized actin bundles followed the geometry of chambers, and then formed several shapes, such as circles, rods, triangles or squares. Since the bundled actins still have motility, we believe this technique is useful for forming a desired pattern of bio-molecular motors toward the actuation of MEMS/NEMS devices.
机译:本文介绍了一种用于控制MEMS器件中的生物纳米驱动单元的丝状电动机蛋白形状的技术。在该实验中,我们使用肌动蛋白,一种构建细胞骨架的蛋白质。肌动蛋白单体(G-肌动蛋白)在高盐条件下聚合并形成细丝(F-Actin);当它们与ATP(腺苷三磷酸酯)溶液中的电机蛋白(肌球蛋白)结合时,长丝移动。 Fascin,推定的捆绑蛋白,紧密地捆绑了几种F-Actins,形成紧身束肌动蛋白[1]。当G-肌动蛋白和粘性溶液局限于聚二甲基硅氧烷(PDMS)或二甲苯微室中,我们发现聚合的肌动蛋白束沿着腔室的几何形状,然后形成几个形状,例如圆圈,杆,三角形或正方形。由于捆绑的Actins仍然具有运动性,因此我们认为该技术可用于形成所需的生物分子电机模式朝向MEMS / NEMS器件的致动。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号