课题基金 / 基金详情

项目摘要

项目成果

Julie Champion的其他基金

相似基金

相关文献

中文摘要
翻译
描述(由申请人提供):本研究的目的是设计横向移动的表面配体,其不仅赋予对细胞行为的控制,而且允许细胞主动重组与其相互作用的表面。配体在生物材料表面的呈现对于细胞粘附和功能是必不可少的。配体的呈现方式显著影响这些过程,从而激发了这项工作。第一个目标是建立一个配体表面对,允许控制,横向配体迁移的基础上化学识别。这将通过设计在细菌中产生的包含细胞相互作用结构域和多个表面结合结构域的模块化配体来实现。细胞相互作用结构域是已知的与细胞表面上的整联蛋白受体结合的肽。表面结合结构域是结合表面锚蛋白的肽。多个表面结合结构域的独立表面附着和脱离将导致横向迁移或“行走”,而整个配体不与表面失去接触。第二个目的是确定配体结构对迁移率的影响。我们假设,功能,如域的顺序和间距,表面结合域的数量和亲和力,肽展示支架将决定配体的流动性。第三个目的是利用这个系统来研究细胞在表面上的行为和细胞操纵移动的配体的能力。表征传统的细胞对生物表面的反应,粘附,扩散和运动,将揭示由于移动的配体对细胞行为的任何新的控制。然而,与传统表面不同,在移动的配体表面上的细胞将有机会主动组织或操纵表面配体。追踪配体和相应的细胞表面受体将提供这种相互作用的证据。公共卫生相关性:这项工作与公共卫生的相关性在于制造用于治疗或组织工程应用的控制细胞行为的生物材料。表面显示横向移动的配体是一种新型的生物表面,不仅支持细胞,但也促进细胞和表面之间的独特的相互作用。
英文摘要
DESCRIPTION (provided by applicant): The objective of this research is to engineer laterally mobile surface ligands that not only confer control over cell behavior but also allow cells to actively reorganize the surface with which they are interacting. Presentation of ligands on biomaterial surfaces is essential for cell adhesion and function. The manner in which ligands are presented significantly affects these processes, thereby motivating this work. The first aim is to create a ligand-surface pair that allows controlled, lateral ligand migration based on chemical recognition. This will be achieved by designing modular ligands, produced in bacteria, that contain a cell interaction domain and multiple surface binding domains. The cell interaction domain is a known binding peptide to an integrin receptor on the cell surface. The surface binding domains are peptides that bind surface anchor proteins. Independent surface attachment and detachment of multiple surface binding domains will result in lateral migration, or "walking", without the entire ligand losing contact with the surface. The second aim is to determine the effect of ligand structure on mobility. We hypothesize that features such as domain order and spacing, number and affinity of surface binding domains, and peptide display scaffolds will dictate ligand mobility. The third aim is to use this system to study cell behavior on the surface and the ability of cells to manipulate mobile ligands. Characterization of traditional cell responses to biosurfaces, adhesion, spreading, and motility, will reveal any new control over cell behavior due to mobile ligands. However, unlike traditional surfaces, cells on the mobile ligand surface will have the opportunity to actively organize or manipulate surface ligands. Tracking the ligands and corresponding cell surface receptors will provide evidence of this type of interaction. PUBLIC HEALTH RELEVANCE: The relevance of this work to public health lies in fabrication of biomaterials that control cell behavior for therapeutic or tissue engineering applications. Surfaces displaying laterally mobile ligands are a new type of biosurface that not only support cells but also promote unique interactions between cells and surfaces.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
2023 Preclinical Form and Formulation for Drug Discovery Gordon Research Conference and Gordon Research Seminar
  • 批准号:
    10605746
  • 项目类别:
  • 资助金额:
    $3.3万
  • 财政年份:
    2023
  • 负责人:
    Julie Champion
  • 依托单位:
Photoelectroporation: Biomacromolecule delivery via nanoscale light-amplified voltage generators
  • 批准号:
    10538761
  • 项目类别:
  • 资助金额:
    $21.56万
  • 财政年份:
    2022
  • 负责人:
    Julie Champion
  • 依托单位:
Photoelectroporation: Biomacromolecule delivery via nanoscale light-amplified voltage generators
  • 批准号:
    10688265
  • 项目类别:
  • 资助金额:
    $18.1万
  • 财政年份:
    2022
  • 负责人:
    Julie Champion
  • 依托单位:
Engineered Protein Nanocarriers for Intracellular Antibody Delivery
  • 批准号:
    9387821
  • 项目类别:
  • 资助金额:
    $22.59万
  • 财政年份:
    2017
  • 负责人:
    Julie Champion
  • 依托单位:
海外基金