Khan Saahir, Sur Shantanu, Dankers Patricia Y W, da Silva Ricardo M P, Boekhoven Job, Poor Taylor A, Stupp Samuel I
Institute for BioNanotechnology in Medicine, Northwestern University 303 East Superior Avenue, Rm. 11-123, Chicago, Illinois 60611, United States.
Bioconjug Chem. 2014 Apr 16;25(4):707-17. doi: 10.1021/bc400507v. Epub 2014 Mar 26.
Post-assembly functionalization of supramolecular nanostructures has the potential to expand the range of their applications. We report here the use of the chemoselective native chemical ligation (NCL) reaction to functionalize self-assembled peptide amphiphile (PA) nanofibers. This strategy can be used to incorporate specific bioactivity on the nanofibers, and as a model, we demonstrate functionalization with the RGDS peptide following self-assembly. Incorporation of bioactivity is verified by the observation of characteristic changes in fibroblast morphology following NCL-mediated attachment of the signal to PA nanofibers. The NCL reaction does not alter the PA nanofiber morphology, and biotinylated RGDS peptide was found to be accessible on the nanofiber surface after ligation for binding with streptavidin-conjugated gold nanoparticles. In order to show that this strategy is not limited to short peptides, we utilized NCL to conjugate yellow fluorescent protein and/or cyan fluorescent protein to self-assembled PA nanofibers. Förster resonance energy transfer and fluorescence anisotropy measurements are consistent with the immobilization of the protein on the PA nanofibers. The change in electrophoretic mobility of the protein upon conjugation with PA molecules confirmed the formation of a covalent linkage. NCL-mediated attachment of bioactive peptides and proteins to self-assembled PA nanofibers allows the independent control of self-assembly and bioactivity while retaining the biodegradable peptide structure of the PA molecule and thus can be useful in tailoring design of biomaterials.
超分子纳米结构的组装后功能化有潜力扩展其应用范围。我们在此报告使用化学选择性天然化学连接(NCL)反应对自组装肽两亲分子(PA)纳米纤维进行功能化。该策略可用于在纳米纤维上引入特定生物活性,作为一个模型,我们展示了自组装后用RGDS肽进行功能化。通过观察NCL介导信号附着到PA纳米纤维后成纤维细胞形态的特征变化,验证了生物活性的引入。NCL反应不会改变PA纳米纤维的形态,并且发现连接后生物素化的RGDS肽在纳米纤维表面可用于与链霉亲和素偶联的金纳米颗粒结合。为了表明该策略不限于短肽,我们利用NCL将黄色荧光蛋白和/或青色荧光蛋白偶联到自组装的PA纳米纤维上。荧光共振能量转移和荧光各向异性测量结果与蛋白质固定在PA纳米纤维上一致。蛋白质与PA分子偶联后电泳迁移率的变化证实了共价键的形成。NCL介导的生物活性肽和蛋白质附着到自组装的PA纳米纤维上,能够在保留PA分子可生物降解肽结构的同时,独立控制自组装和生物活性,因此可用于生物材料的定制设计。