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首页> 外文期刊>ACS nano >BMHP1-derived self-assembling peptides: Hierarchically assembled structures with self-healing propensity and potential for tissue engineering applications
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BMHP1-derived self-assembling peptides: Hierarchically assembled structures with self-healing propensity and potential for tissue engineering applications

机译:BMHP1衍生的自组装肽:具有自修复倾向并具有组织工程应用潜力的分层组装结构

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Self-assembling peptides (SAPs) are rapidly gaining interest as bioinspired scaffolds for cell culture and regenerative medicine applications. Bone Marrow Homing Peptide 1 (BMHP1) functional motif (PFSSTKT) was previously demonstrated to stimulate neural stem cell (NSC) viability and differentiation when linked to SAPs. We here describe a novel ensemble of SAPs, developed from the BMHP1 (BMHP1-SAPs), that spontaneously assemble into tabular fibers, twisted ribbons, tubes and hierarchical self-assembled sheets: organized structures in the nano- and microscale. Thirty-two sequences were designed and evaluated, including biotinylated and unbiotinylated sequences, as well as a hybrid peptide-peptoid sequence. Via X-ray diffraction (XRD), CD, and FTIR experiments we demonstrated that all of the BMHP1-SAPs share similarly organized secondary structures, that is, β-sheets and β-turns, despite their heterogeneous nanostructure morphology, scaffold stiffness, and effect over NSC differentiation and survival. Notably, we demonstrated the self-healing propensity of most of the tested BMHP1-SAPs, enlarging the set of potential applications of these novel SAPs. In in vitro cell culture experiments, we showed that some of these 10-mer peptides foster adhesion, differentiation, and proliferation of human NSCs. RGD-functionalized and hybrid peptide-peptoid self-assembling sequences also opened the door to BMHP1-SAP functionalization with further bioactive motifs, essential to tailor new scaffolds for specific applications. In in vivo experiments we verified a negligible reaction of the host nervous tissue to the injected and assembled BMHP1-SAP. This work will pave the way to the development of novel SAP sequences that may be useful for material science and regenerative medicine applications.
机译:自组装肽(SAPs)作为用于细胞培养和再生医学应用的生物启发支架而迅速受到关注。先前已证明,骨髓归巢肽1(BMHP1)功能性基序(PFSSTKT)在与SAP连接时可刺激神经干细胞(NSC)的活力和分化。我们在这里描述了从BMHP1(BMHP1-SAPs)开发来的SAP的新集合,它自发地组装成板状纤维,扭曲的带子,管子和分层的自组装薄板:纳米和微米级的有组织结构。设计和评估了32个序列,包括生物素化和非生物素化的序列,以及杂合肽-类肽序列。通过X射线衍射(XRD),CD和FTIR实验,我们证明了所有BMHP1-SAP都具有相似的有序二级结构,即β-折叠和β-转弯,尽管它们具有异质的纳米结构形态,支架刚度和对NSC分化和存活的影响。值得注意的是,我们展示了大多数测试的BMHP1-SAP的自我修复倾向,从而扩大了这些新型SAP的潜在应用范围。在体外细胞培养实验中,我们表明这些10-mer肽中的某些可促进人NSC的粘附,分化和增殖。 RGD功能化和杂合肽-类肽自组装序列也为BMHP1-SAP功能化打开了大门,该功能具有进一步的生物活性基序,这对于为特定应用定制新支架至关重要。在体内实验中,我们验证了宿主神经组织对注射和组装的BMHP1-SAP的反应可忽略不计。这项工作将为开发可能对材料科学和再生医学应用有用的新型SAP序列铺平道路。

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