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Development, characterization and applications of a direct, general method to photochemically generate patterns and gradients on planar glass substrates, corrugated substrates and in highly porous collagen-GAG scaffolds

机译:在平面玻璃基板,瓦楞基板和高度多孔胶原-GaG支架上光化学生成图案和梯度的直接通用方法的开发,表征和应用

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摘要

Recent surface chemical approaches to physically modeling the extra-cellular matrix (ECM) have provided invaluable insight into the molecular nature of cell adhesion and have clearly established the contributions of altered cell adhesion to disease onset and progression. In order to better understand the complex relationships between the many molecules involved in cell adhesion, we have developed a general method to create multi-component biological surface gradients that present multiple, distinct adhesive molecules onto planar substrates, corrugated substrates and the surface of collagen-GAG scaffolds at varied concentrations, and in defined geometric patterns. In our approach the generation of a light density gradient across a photo-active benzophenone monolayer will form covalent linkages between a solution phase biomolecule and the surface, resulting in the transfer of the photon gradient to a biomolecular gradient. The method is promising for the direct generation of complex, multi-component patterns or gradients of biomolecules, which may serve as biomolecularly relevant models of the ECM. Future work will focus on applying multi-component biomolecular patterns and gradients to investigations of cell adhesion, migration, proliferation, and differentiation.
机译:物理建模细胞外基质(ECM)的最新表面化学方法为细胞粘附的分子性质提供了宝贵的见解,并清楚地确定了细胞粘附改变对疾病发作和进展的贡献。为了更好地理解细胞粘附中涉及的许多分子之间的复杂关系,我们开发了一种通用方法来创建多组分生物表面梯度,该梯度将多个不同的粘附剂分子呈现在平面基材,波纹状基材和胶原蛋白表面上GAG脚手架的浓度不同,几何形状也不同。在我们的方法中,在光活性二苯甲酮单分子层上产生光密度梯度将在溶液相生物分子和表面之间形成共价键,从而导致光子梯度转移到生物分子梯度。该方法有望直接产生复杂的,多组分的生物分子图谱或梯度,可以作为ECM的生物分子相关模型。未来的工作将集中于将多组分生物分子模式和梯度应用于细胞粘附,迁移,增殖和分化的研究。

著录项

  • 作者

    Martin Teresa A.;

  • 作者单位
  • 年度 2011
  • 总页数
  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
  • 中图分类

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