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短肽与多金属氧酸盐的超分子共聚:水下黏合剂的制备。

Supramolecular Copolymerization of Short Peptides and Polyoxometalates: toward the Fabrication of Underwater Adhesives.

机构信息

State Key Laboratory of Supramolecular Structure and Materials, Institute of Theoretical Chemistry, Jilin University , Qianjin Avenue 2699, Changchun 130012, China.

National Analytical Research Center of Electrochemistry and Spectroscopy, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences , 5625 Renmin Street, Changchun 130022, China.

出版信息

Biomacromolecules. 2017 Nov 13;18(11):3524-3530. doi: 10.1021/acs.biomac.7b00817. Epub 2017 Sep 15.

DOI:10.1021/acs.biomac.7b00817
PMID:28879768
Abstract

Peptide assembly has reached exquisite levels of efficiency in the creation of bioactive materials. However, we have not yet been able to take what we have learned from peptide assembly to develop a general strategy for the fabrication of biomimetic underwater adhesives, which retain significant advantages as medical glue for clinical treatment. Herein we report a simple approach to prepare peptide-based adhesives through the supramolecular polymerization of cationic peptides drove by polyoxometalates (PMs). Mass spectra, Fourier-transform infrared spectra and W NMR spectra confirmed the structural integrity of peptides and PMs during the coassembly process. Scanning electron microscopy demonstrated that the multivalent interactions between peptides and polyoxometaltes led to the formation of robust 3D network structures. The rheological study revealed that the peptide/PM assemblies exhibited mechanically rigid gel-like behavior and self-healing property. Interestingly, the assemblies showed the capacity to adhere various wet solid materials under waterline. The shear strength of the peptide-based adhesives are stronger than that of the commercially available fibrin glue. This finding is exciting and serves to expand our capability of the fabrication of peptide-based materials.

摘要

在生物活性材料的制备中,肽的自组装已经达到了非常高的效率。然而,我们还没有能够从肽的自组装中吸取经验,发展出一种通用的仿生水下粘合剂的制造策略,这种水下粘合剂作为医用胶在临床治疗中有很大的优势。在此,我们报道了一种通过多酸(PMs)驱动的阳离子肽的超分子聚合来制备基于肽的粘合剂的简单方法。质谱、傅里叶变换红外光谱和 W NMR 光谱证实了肽和 PMs 在共组装过程中的结构完整性。扫描电子显微镜表明,肽和多酸之间的多价相互作用导致了坚固的 3D 网络结构的形成。流变学研究表明,肽/PM 组装体表现出机械刚性的凝胶状行为和自修复特性。有趣的是,这些组装体在水下能够黏附各种湿固材料。基于肽的粘合剂的剪切强度强于市售的纤维蛋白胶。这一发现令人兴奋,为我们制造基于肽的材料的能力提供了扩展。

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