Synthesis and Characterization of Molecular Building Blocks for Responsive Materials

响应材料分子构件的合成和表征

基本信息

项目摘要

Responsive materials can exhibit large changes in their volume and generate force with small environmental changes (e.g. temperature, pH, light, or other solution property). These materials have found applications as biomaterials, drug delivery devices, and in microfluidic devices. The most common materials currently used are randomly crosslinked polymer hydrogels. Their major limitation is their slow response time, poor directionality and the small volume changes. The limitations probably being slow diffusion and aggregation of polymers and also water diffusion.The objective of this collaboration is to overcome these limitations by developing molecular scale responsive subunits. They can operate without polymer diffusion and allow to form dilute gels, which make the polymer and water diffusion not limiting anymore. Therefore, these materials will respond much more quickly and exhibit a greater size reduction than the traditional responsive hydrogels.In a combined effort, the molecular building blocks were designed using structures from various natural proteins. In the lab of Prof. Holland (Cleveland State University) the artificial proteins are encoded in DNA and produced in bacterial expression systems. The lab of Prof. Hugel (Technische Universität München) characterizes the behavior of these new materials with AFM-based single polymer force measurements. As a team, the groups will illustrate various applications of the materials including optically driven molecular motors, fast response hydrogels for controlled release, and oriented responsive fibres for large and fast directional actuators.
响应性材料可以在其体积上表现出大的变化,并且在小的环境变化(例如温度、pH、光或其他溶液性质)下产生力。这些材料已被用作生物材料、药物递送装置和微流体装置。目前使用的最常见的材料是无规交联聚合物水凝胶。它们的主要局限性是响应时间慢、方向性差和体积变化小。限制可能是缓慢的扩散和聚合物的聚集和水的扩散。这项合作的目标是通过开发分子尺度的响应亚基来克服这些限制。它们可以在没有聚合物扩散的情况下操作,并允许形成稀释的凝胶,这使得聚合物和水的扩散不再受到限制。因此,与传统的响应性水凝胶相比,这些材料的响应速度更快,尺寸更小。在一项综合努力中,分子构建模块是使用各种天然蛋白质的结构设计的。在克利夫兰州立大学Holland教授的实验室中,人工蛋白质在DNA中编码,并在细菌表达系统中产生。Hugel教授(慕尼黑工业大学)的实验室通过基于AFM的单聚合物力测量来表征这些新材料的行为。作为一个团队,这些小组将说明材料的各种应用,包括光学驱动分子马达,用于控制释放的快速响应水凝胶,以及用于大型和快速定向致动器的定向响应纤维。

项目成果

期刊论文数量(2)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
The effect of temperature on single-polypeptide adsorption.
温度对单多肽吸附的影响
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Professor Dr. Thorsten Hugel其他文献

Professor Dr. Thorsten Hugel的其他文献

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{{ truncateString('Professor Dr. Thorsten Hugel', 18)}}的其他基金

Thermal and directed motion in molecular friction processes investigated by atomic and photonic force microscopy
通过原子和光子力显微镜研究分子摩擦过程中的热运动和定向运动
  • 批准号:
    420798410
  • 财政年份:
    2019
  • 资助金额:
    --
  • 项目类别:
    Research Grants
OXPL - Molecular level physiology and pathology of oxidized phospholipids
OXPL - 氧化磷脂的分子水平生理学和病理学
  • 批准号:
    128019854
  • 财政年份:
    2009
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Energy conversion of E. coli Hsp90 and yeast Hsp90
大肠杆菌 Hsp90 和酵母 Hsp90 的能量转换
  • 批准号:
    141825192
  • 财政年份:
    2009
  • 资助金额:
    --
  • 项目类别:
    Research Grants
AFM-based determination of interface and interphase interactions
基于 AFM 的界面和相间相互作用测定
  • 批准号:
    67458160
  • 财政年份:
    2008
  • 资助金额:
    --
  • 项目类别:
    Priority Programmes
Single Polymer Friction at Interfaces
单聚合物界面摩擦
  • 批准号:
    35368947
  • 财政年份:
    2006
  • 资助金额:
    --
  • 项目类别:
    Research Grants
The DNA-packoging motor of the bacteriophage phi29
噬菌体 phi29 的 DNA 包装马达
  • 批准号:
    5409943
  • 财政年份:
    2003
  • 资助金额:
    --
  • 项目类别:
    Emmy Noether International Fellowships

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