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Development of Protein-Displaying Peptide Hydrogels for Tissue Engineering

Development of Protein-Displaying Peptide Hydrogels for Tissue Engineering
用于组织工程的蛋白质展示肽水凝胶的开发
批准号:
8054835
负责人:
Jonathan Kyle Pokorski
金额:
$8.97万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-04-01 至 2012-02-14

项目摘要

项目成果

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中文摘要
翻译
描述(申请人提供):用于组织工程的新型生物材料的开发是一个新兴的研究领域,对美国的公共健康具有广泛的影响。该领域的进展有可能治疗各种医疗疾病,如皮肤损伤(即撕裂和烧伤)、心脏创伤、严重脊柱损伤和骨折。目前,用于组织工程的大多数合成材料都是将生长因子或多肽结合到材料基质中的聚合物。掺入模式的范围从共价(对于小肽)到吸附(对于较大的感兴趣蛋白质)。如果全长蛋白质能够以高亲和力和高特异性结合并展示在组织工程平台中,该领域将得到显着的进步。近年来,刺激响应性多肽水凝胶在材料科学和组织工程领域受到越来越多的关注。这些类型的材料组装成纳米级纤维,然后水合形成坚硬的凝胶材料。这些材料的优点包括:易于获得纯单体单元、无毒、可注射,在某些情况下还具有抗菌性能。然而,缺乏的是通过高亲和力的非共价结合作用来结合和展示功能蛋白的能力。在拟议研究计划的指导阶段,将使用来自噬菌体Q?的病毒样颗粒(VLP)开发噬菌体展示技术,噬菌体Q?是芬兰实验室主要用于各种生物技术应用的病毒纳米颗粒。该提案旨在开发一个平台,用于在Q?VLP用于定向进化实验,以识别与凝胶形成肽MAX8特异相互作用的变体。我们将在Q?表面展示选定的多肽。并评估结合亲和力和凝胶掺入之间的关系。然后,将严格表征新合成材料的材料特性。拟议研究的独立阶段将直接从指导阶段的结果发展起来。在我的团队中发起的这项研究计划将利用获得的关于将大分子结合到水凝胶中的多肽亲和标签的信息来开发一种新的组织工程方法。在指导阶段识别的多肽亲和标签将在一端或两端与骨形态发生蛋白2(BMP2)融合,并作为凝胶原纤维形成的成核位置。修饰后的BMP2蛋白将被整合到多肽水凝胶中,并对材料的相关性能进行评估,如蛋白质释放和负载能力。这些新材料将作为组织培养实验的支架,促进骨祖细胞的生长和分化。这种特殊方法的一个优点是,材料是通过简单地混合凝胶成分来配制的,因此使得加入多种生长因子变得容易。这将在未来的化身中扩展,包括多种生长因子,以更好地模拟天然的细胞外基质。 与公共健康相关:组织工程生物材料的开发是一个新兴的研究领域,对美国的公共健康具有广泛的影响。该领域尚处于起步阶段,但有可能影响各种疾病的治疗,这些疾病需要损伤组织的重新生长,如脊髓损伤或烧伤创伤。这项建议描述了一种新的方法,将负责指导特定组织生长的蛋白质呈现在可注射凝胶中,用于潜在的治疗用途。
英文摘要
DESCRIPTION (provided by applicant): The development of novel bio-materials for tissue engineering is a burgeoning research field with broad impact on public health in the United States. Advances in the field have the potential to treat myriad medical conditions such as dermal injuries (i.e. lacerations and burns), cardiac trauma, severe spinal injuries, and bone breaks. Currently, most synthetic materials used for tissue engineering are polymers that incorporate growth factors or peptides into a material matrix. The mode of incorporation ranges from covalent (for small peptides) to adsorptive (for larger proteins of interest). The field would be significantly advanced if full-length proteins could be incorporated and displayed within tissue engineering platforms both with high affinity and specificity. Stimulus-responsive peptide hydrogels have received increasing attention in the materials science and tissue engineering communities of late. These types of materials assemble into nano-scale fibers that are hydrated to form rigid gel materials. The advantages of these materials include, facile access to pure monomer units, non- toxicity, injectability, and in certain cases, anti-bacterial properties. What lacks, however, is the ability to incorporate and display functional proteins through high-affinity non-covalent binding interactions. In the mentored phase of the proposed research program, phage display technology will be developed using virus- like particles (VLPs) derived from bacteriophage Q?, a viral nanoparticle principally utilized by the Finn laboratory for myriad bio-technological applications. The proposal aims to develop a platform for the display of peptide libraries on the exterior surfaces of Q? VLPs for use in directed evolution experiments to identify variants that interact specifically with a gel-forming peptide, MAX8. We will display the selected peptides on the surface of Q? VLPs and evaluate how binding affinity and gel-incorporation are correlated. The material properties of the newly synthesized materials will then be rigorously characterized. The independent phase of the proposed research will grow directly from the results of the mentored phase. The research program initiated in my group will use information garnered about the use of peptide affinity tags for incorporation of macromolecules into hydrogels to develop a novel tissue engineering approach. The peptide affinity tags identified in the mentored phase will be fused to bone morphogenetic protein 2 (BMP2) at one or both termini, and act as nucleation sites for gel fibril formation. The modified BMP2 proteins will be integrated into peptide hydrogels and the materials evaluated for relevant properties such as protein release and loading capacity. These new materials will serve as scaffolds in tissue culture experiments to promote the growth and differentiation of osteo-progenitor cells. An advantage of this particular approach is that materials are formulated by simple mixing of gelling components, thus making incorporation of multiple growth factors facile. This will be extended in future incarnations to include multiple growth factors to better mimic the native extracellular matrix. PUBLIC HEALTH RELEVANCE: The development of bio-materials for tissue engineering is a burgeoning research field with broad impact on public health in the United States. The field is in its infancy, but has the potential to affect the treatment of a variety of ailments that require the re-growth of injured tissue such as spinal cord injury or burn trauma. This proposal describes a novel way to present proteins responsible for directing the growth of specific tissues, within injectable gels for potential therapeutic use.
期刊论文(1)
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科研奖励(0)
会议论文
DOI: 10.1021/mp100225y
发表时间: 2011-02-07
期刊: Molecular pharmaceutics
影响因子: 4.9
作者: [Pokorski JK, Steinmetz NF]
通讯作者: Steinmetz NF
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Development of Protein-Displaying Peptide Hydrogels for Tissue Engineering
  • 批准号:
    8413259
  • 项目类别:
  • 资助金额:
    $24.87万
  • 财政年份:
    2012
  • 负责人:
    Jonathan Kyle Pokorski
  • 依托单位:
Development of Protein-Displaying Peptide Hydrogels for Tissue Engineering
  • 批准号:
    8425104
  • 项目类别:
  • 资助金额:
    $23.2万
  • 财政年份:
    2012
  • 负责人:
    Jonathan Kyle Pokorski
  • 依托单位:
海外基金