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Characterizing and controlling structural and mechanical properties of type I collagen self-assembly.

机译:表征和控制I型胶原蛋白自组装的结构和机械性能。

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摘要

Type I collagen matrices are used across a variety of applications in bioengineering and biophysical studies; however, a fuller understanding of the collagen self-assembly process is required to optimize control of the matrix structural and mechanical properties in these applications. The work in this thesis sought to 1) characterize collagen self-assembly using simultaneous imaging, spectroscopy, and rheological methods, 2) use collagen gels as three-dimensional microenvironments to study glioma invasion, and 3) develop a model using experimental research data to teach data analysis tools to undergraduate students.;Chapter 1 provides a brief overview of collagen in the body, its applications, structural details about the collagen monomer, and descriptions of in vivo and in vitro fibrillogenesis. Advantages and disadvantages of methodologies used to study collagen self-assembly are discussed for in vitro fibrillogenesis. The materials and methods used in this thesis are described in Chapter 2.;Chapters 3 and 4 describe insights into collagen self-assembly using multiple modalities. In Chapter 3, turbidity and confocal reflectance microscopy were simultaneously employed to track collagen fibrillogenesis and reconcile the information reported by the two techniques, with confocal fluorescence microscopy used to supplement information about early events in fibrillogenesis. Chapter 4 describes the novel use of simultaneous rheology and confocal microscopy to study the development of mechanical and structural properties of collagen gels.;In Chapter 5, glioma migratory and invasive behaviors are observed and perturbed in the context of well-controlled in vitro two- and three-dimensional environments, including implanting multicellular tumor spheroids in collagen gels across several concentrations to test the effects of pore size on glioma invasion. This chapter serves as a preliminary investigation into how glioma behavior changes depending on environment dimensionality and lays out further studies to fully investigate the mechanisms underlying glioma invasion.;Finally, Chapter 6 describes the development, evaluation, and redesign of a Microsoft Excel-based activity where data analysis from contemporary research (published in Chapter 3) was adapted into a training exercise for students taking an introductory General Chemistry Laboratory course. This activity humanized the research enterprise for the undergraduate students and can serve as a model for future collaborations between research and instructional laboratories.
机译:I型胶原蛋白基质在生物工程和生物物理研究中广泛使用;然而,在这些应用中,需要对胶原蛋白自组装过程有更全面的了解,以优化对基质结构和机械性能的控制。本论文的工作旨在:1)使用同步成像,光谱学和流变学方法表征胶原蛋白的自组装,2)使用胶原蛋白凝胶作为三维微环境来研究神经胶质瘤的侵袭,以及3)使用实验研究数据开发模型来向大学生讲授数据分析工具。;第1章简要概述了体内胶原蛋白,胶原蛋白的应用,胶原蛋白单体的结构细节以及体内和体外原纤维形成的描述。讨论了用于研究胶原自组装的方法的优缺点,用于体外原纤维形成。本论文中使用的材料和方法在第2章中进行了描述。第3章和第4章介绍了使用多种模式对胶原蛋白自组装的见解。在第三章中,同时使用浊度和共聚焦反射显微镜跟踪胶原原纤维形成,并协调两种技术报告的信息,共聚焦荧光显微镜用于补充有关原纤维形成早期事件的信息。第4章介绍了同时使用流变学和共聚焦显微镜研究胶原蛋白凝胶的机械和结构特性的新方法。第5章在控制良好的体外两个条件下观察并干扰了神经胶质瘤的迁移和侵袭行为。三维环境,包括将多种浓度的胶原蛋白凝胶中植入多细胞肿瘤球体,以测试孔径对神经胶质瘤侵袭的影响。本章是对神经胶质瘤行为根据环境维度的变化方式进行的初步调查,并提出了进一步的研究以充分调查神经胶质瘤入侵的潜在机制。最后,第6章介绍了基于Microsoft Excel的活动的开发,评估和重新设计。将当代研究的数据分析(在第3章中发布)改编成针对参加通用化学实验室入门课程的学生的培训练习。该活动使本科生的研究企业变得人性化,并且可以作为研究与教学实验室之间未来合作的模型。

著录项

  • 作者

    Zhu, Jieling.;

  • 作者单位

    Columbia University.;

  • 授予单位 Columbia University.;
  • 学科 Chemistry.
  • 学位 Ph.D.
  • 年度 2015
  • 页码 179 p.
  • 总页数 179
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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