CAREER: Using Functionalized Protein-based Materials to Control and Pattern Cell Behavior
CAREER: Using Functionalized Protein-based Materials to Control and Pattern Cell Behavior
批准号:
1151394
负责人:
Sarah Bondos
金额:
$50.0万
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-02-15 至 2017-08-31
中文摘要
该职业奖由德克萨斯a&m健康科学中心材料研究部生物材料项目颁发,旨在开发在三维支架中结合和绘制活性结构蛋白的方法,从而极大地扩展了在细胞生物学和组织工程研究中操纵细胞行为的能力。生成或功能化材料的常见方法可能会损害敏感分子。细胞因子,控制生长、迁移、凋亡和分化的蛋白质,尤其脆弱。有了这个奖项,功能化材料将使用果蝇蛋白Ultrabithorax (Ubx)在一个步骤中制备。Ubx在温和的缓冲液中快速自组装,允许基因融合到Ubx的细胞因子保持活性。细胞因子- ubx融合材料将用于三维支架内的血管生成。蛋白质的特性将被定义为允许掺入,基准细胞因子相对于可溶性单体嵌入材料的活性,并评估未表征的细胞因子调节血管生成的能力。通过与本科实验课程合作,该项目每年将使60-70名学生在学习基本生物化学技术的同时参与前沿研究。优秀的学生将被邀请在学年和暑期实习期间继续他们的研究。构建人造组织或器官需要一个支架,理想情况下,它既能在三维空间上支持细胞,又能指导细胞的行为。这些“指令”通常是功能强大的蛋白质,它们与细胞相互作用,控制细胞的附着、身份、形状、运动和生长。然而,很难将这些蛋白质附着在支架上而不损坏它们。研究人员开发了一种独特的材料,可以在温和的条件下快速组装,使人们可以在不伤害蛋白质的情况下附着各种蛋白质。该建议将这些指导性蛋白定位在一个三维支架中,以控制和模式细胞行为。由此产生的材料也将允许识别对细胞有用的新蛋白质。从长远来看,在这个提议中发展的方法可以适用于在相同的支架中构建细胞(例如,在肝细胞块中构建血管),这是制造人造组织和器官的必要步骤。作为这项研究的一部分,研究生和本科生将接受跨学科的培训。研究是STEM培训的重要组成部分,但本科生的数量超过了研究机会的数量。与拥有大量少数族裔学生的休斯顿大学的一个班级合作,每年将允许60-70名本科生参与这项研究,同时学习实验室技能。
英文摘要
This Career award by the Biomaterials program in the Division of Materials Research to the Texas A&M Health Science Center is to develop methods in incorporation and patterning active, structured proteins in a three-dimensional scaffold, thus greatly extending the ability to manipulate cell behavior in cell biology and tissue engineering studies. Common approaches in generating or functionalizing materials can harm sensitive molecules. Cytokines, proteins that control growth, migration, apoptosis, and differentiation, are particularly vulnerable. With this award, functionalized materials will be prepared in a single step using the Drosophila protein Ultrabithorax (Ubx). Ubx rapidly self-assembles in mild buffers, allowing cytokines that have been genetically fused to Ubx to remain active. Cytokine-Ubx fusion materials will be used to direct and pattern angiogenesis within a three-dimensional scaffold. The properties of proteins will defined that permit incorporation, benchmark the activity of cytokines embedded in materials relative to soluble monomers, and assess the ability of uncharacterized cytokines to regulate angiogenesis. By collaborating with an undergraduate laboratory course, this project will enable 60-70 students per year to participate in cutting-edge research while learning basic biochemistry techniques. Outstanding students will be invited to continue their research during the school year and in summer internships.Building artificial tissues or organs requires a scaffold, which ideally would both support cells in three dimensions and instruct cell behavior. These "instructions" are often powerful proteins which interact with the cell to control cell attachment, identity, shape, movement, and growth. However, it is difficult to attach these proteins to a scaffold without damaging them. The investigator has developed a unique material that assembles itself quickly in gentle conditions, allowing one to attach a variety of proteins without harming them. This proposal will position these instructive proteins in a three dimensional scaffold to control and pattern cell behavior. The resulting materials will also allow in identifying new proteins with useful effects on cells. In the long term, the methods developed in this proposal could be adapted to pattern cells in the same scaffold (for instance, build blood vessels in a block of liver cells), a necessary step in producing artificial tissues and organs. As part of this research, graduate and undergraduate students will receive interdisciplinary training. Research is a critical component of STEM training, but the number of undergraduates exceeds the number of research opportunities. Collaboration with a class at University of Houston, which has a large minority student population, will allow 60-70 undergraduates per year to participate in this research as they learn laboratory skills.
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Separating full-length protein from aggregating proteolytic products using filter flow-through purification
使用过滤流通纯化从聚集的蛋白水解产物中分离全长蛋白质
DOI:
10.1016/j.ab.2016.09.009
发表时间:
2016
期刊:
Analytical Biochemistry
影响因子:
2.9
作者:
[Churion, Kelly A., Rogers, Robert E., Bayless, Kayla J., Bondos, Sarah E.]
通讯作者:
Bondos, Sarah E.
Materials composed of the D rosophila Hox protein Ultrabithorax are biocompatible and nonimmunogenic: UBX Materials are Biocompatible and Non-Immunogenic
由果蝇 Hox 蛋白 Ultrabithorax 组成的材料具有生物相容性和非免疫原性: UBX 材料具有生物相容性和非免疫原性
DOI:
10.1002/jbm.a.35295
发表时间:
2015
期刊:
Journal of Biomedical Materials Research Part A
影响因子:
4.9
作者:
[Patterson, Jan L., Arenas-Gamboa, Angela M., Wang, Ting-Yi, Hsiao, Hao-Ching, Howell, David W., Pellois, Jean-Philippe, Rice-Ficht, Allison, Bondos, Sarah E.]
通讯作者:
Bondos, Sarah E.
The Effect of Protein Fusions on the Production and Mechanical Properties of Protein-Based Materials
蛋白质融合对蛋白质基材料的生产和机械性能的影响
DOI:
10.1002/adfm.201402997
发表时间:
2015
期刊:
Advanced Functional Materials
影响因子:
19
作者:
[Tsai, Shang-Pu, Howell, David W., Huang, Zhao, Hsiao, Hao-Ching, Lu, Yang, Matthews, Kathleen S., Lou, Jun, Bondos, Sarah E.]
通讯作者:
Bondos, Sarah E.
Materials composed of the Drosophila melanogaster protein ultrabithorax are cytocompatible: Ubx Protein Materials are Cytocompatible
由果蝇蛋白 ultrabithorax 组成的材料具有细胞相容性:Ubx 蛋白材料具有细胞相容性
DOI:
10.1002/jbm.a.34675
发表时间:
2014
期刊:
Journal of Biomedical Materials Research Part A
影响因子:
4.9
作者:
[Patterson, Jan L., Abbey, Colette A., Bayless, Kayla J., Bondos, Sarah E.]
通讯作者:
Bondos, Sarah E.
I-Corps: High affinity and high specificity ligand binding materials
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批准号:1724662
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项目类别:Standard Grant
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资助金额:$5.0万
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财政年份:2017
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负责人:Sarah Bondos
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依托单位:
国内基金
海外基金
Capture and Release of Droplets Using Advanced Materials for High Technology Applications
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批准号:52073127
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项目类别:面上项目
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资助金额:58.0万元
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批准年份:2020
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负责人:Alidad Amirfazli
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依托单位:
Molecular Interaction Reconstruction of Rheumatoid Arthritis Therapies Using Clinical Data
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批准号:31070748
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项目类别:面上项目
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资助金额:34.0万元
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批准年份:2010
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负责人:Christine Nardini
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依托单位: