Development of Protein-Displaying Peptide Hydrogels for Tissue Engineering
Development of Protein-Displaying Peptide Hydrogels for Tissue Engineering
批准号:
7871541
负责人:
Jonathan Kyle Pokorski
金额:
$8.78万
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 2012-03-31
关键词:
AdsorptionAffectAffinityAnti-Bacterial AgentsAttentionBacteriophagesBindingBiocompatible MaterialsBurn TraumaBurn injuryCardiacCommunitiesComplexDermalDevelopmentDifferentiation and GrowthEnvironmentExtracellular MatrixFiberFutureGelGoalsGrowthGrowth FactorHydrogelsInjectableInjuryLaboratoriesLacerationLeadLengthMedicalMentorsModelingNatural regenerationPeptide LibraryPeptide Phage Display LibraryPeptidesPhage DisplayPhasePolymersPropertyProteinsPublic HealthRecombinant Growth FactorResearchScienceSiteSpecificitySpinal InjuriesSpinal cord injuryStem cellsStimulusSurfaceSystemTechnologyTherapeutic UsesTissue EngineeringTissuesToxic effectTraumaUnited StatesVariantVirus-like particlebonebone morphogenetic protein 2cell growthdirected evolutionimplantationimprovedinfancyinjuredinterestmacromoleculemonomernanofibernanoscalenovelosteoprogenitor cellprogramsprotein aminoacid sequencepublic health relevanceresearch studyscaffoldtissue cultureviral nanoparticle
中文摘要
描述(由申请人提供):组织工程新型生物材料的开发是一个新兴的研究领域,对美国的公共卫生有着广泛的影响。该领域的进步有可能治疗无数的医疗状况,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,大多数用于组织工程的合成材料都是将生长因子或肽结合到材料基质中的聚合物。结合模式范围从共价(用于小肽)到吸附(用于感兴趣的较大蛋白质)。如果全长蛋白能够以高亲和力和特异性被整合并在组织工程平台上展示,该领域将取得重大进展。刺激反应肽水凝胶近年来在材料科学和组织工程界受到越来越多的关注。这些类型的材料组装成纳米级纤维,水合形成刚性凝胶材料。这些材料的优点包括易于获得纯单体,无毒,可注射,并且在某些情况下具有抗菌特性。然而,缺乏的是通过高亲和力非共价结合相互作用整合和展示功能蛋白的能力。在拟议研究计划的指导阶段,噬菌体展示技术将利用从噬菌体Q?这是一种病毒纳米颗粒,主要被芬兰实验室用于无数生物技术应用。该提案旨在开发一个肽库在Q?VLPs用于定向进化实验,以识别与凝胶形成肽MAX8特异性相互作用的变体。我们将在Q?VLPs和评估结合亲和力和凝胶结合是如何相关的。然后对新合成材料的材料性质进行严格的表征。建议研究的独立阶段将直接从指导阶段的结果中成长。我小组发起的研究项目将利用利用肽亲和标签将大分子结合到水凝胶中的信息来开发一种新的组织工程方法。在指导阶段鉴定的肽亲和标签将在一个或两个末端融合到骨形态发生蛋白2 (BMP2),并作为凝胶纤维形成的成核位点。修饰后的BMP2蛋白将被整合到肽水凝胶中,并评估材料的相关特性,如蛋白质释放和负载能力。这些新材料将在组织培养实验中作为促进骨祖细胞生长和分化的支架。这种特殊方法的一个优点是,材料是通过简单的混合胶凝成分配制的,从而使多种生长因子的结合变得容易。这将在未来的化身中扩展,包括多种生长因子,以更好地模拟原生细胞外基质。
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.
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海外基金