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PEPTIDE-BASED METHODS FOR ASSEMBLING AND CONTROLLING THE MORPHOLOGIES, METRICS, AND PROPERTIES OF GOLD NANOPARTICLE SUPERSTRUCTURES

机译:基于肽的金纳米粒子超结构的形态,度量和性质的组装和控制方法

摘要

This dissertation describes new peptide-based methods for assembling and controlling the morphologies, metrics, and properties of gold nanoparticle superstructures. The aim of this research is to develop the peptide-based method by modifying the peptide sequences and controlling the reaction conditions for the synthesis and assembly of gold nanoparticle superstructures to achieve reliable control over their morphology and metrics, and furthermore study their properties and applications.udWith this goal in mind, the C-terminus of a gold-binding peptide was modified with different numbers of hydrophobic phenylalanines to affect peptide assembly and ultimately nanoparticle assembly. The addition of hydrophobic phenylalanines to the C-terminus of peptide conjugates promoted fiber bundling which in turn lead to the formation of thick or intertwined 1-D nanoparticle superstructures. Furthermore, I prepared spherical gold nanoparticle superstructures with varied diameters (~40nm, ~75nm, and ~150nm) and visible to near-infrared optical properties by using a single peptide conjugate molecule yet varied reaction conditions. Theoretical simulation and experiment were coupled to further understand their optical properties. Finally, I studied and demonstrated the drug storage and release properties of hollow spherical gold nanoparticle superstructures; this was the first demonstrated application of this class of nanoparticle superstructure.ud
机译:本文介绍了基于肽的新方法,用于组装和控制金纳米粒子超结构的形貌,量度和性能。这项研究的目的是通过修饰肽序列并控制金纳米颗粒超结构的合成和组装的反应条件,以实现对其形态和度量的可靠控制,从而开发基于肽的方法,并进一步研究其性质和应用。出于这个目标,用不同数量的疏水性苯丙氨酸修饰了金结合肽的C末端,以影响肽的组装并最终影响纳米颗粒的组装。将疏水性苯丙氨酸添加到肽缀合物的C末端可促进纤维束聚,进而导致形成厚的或缠结的1-D纳米粒子超结构。此外,我通过使用单个肽结合物分子和不同的反应条件,制备了直径可变(〜40nm,〜75nm和〜150nm)的球形金纳米粒子超结构,并具有可见到近红外的光学特性。理论模拟和实验相结合,以进一步了解它们的光学性质。最后,我研究并论证了中空球形金纳米粒子超结构的储藏和释放特性。这是此类纳米粒子超结构的首次展示应用。 ud

著录项

  • 作者

    Zhang Chen;

  • 作者单位
  • 年度 2015
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
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