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混合含核碱基的肽时的共组装和多组分水凝胶形成。

Co-assembly and multicomponent hydrogel formation upon mixing nucleobase-containing peptides.

机构信息

Université de Lorraine, CNRS, LCPM, F-54000 Nancy, France.

Université de Lorraine, CNRS, CRM2, F-54000 Nancy, France.

出版信息

Nanoscale. 2021 Jun 17;13(23):10566-10578. doi: 10.1039/d1nr02417e.

Abstract

Peptide-based hydrogels are physical gels formed through specific supramolecular self-assembling processes, leading to ordered nanostructures which constitute the water entrapping scaffold of the soft material. Thanks to the inherent properties of peptides, these hydrogels are highly considered in the biomedical domain and open new horizons in terms of application in advanced therapies and biotechnologies. The use of one, and only one, native peptide to formulate a gel is by far the most reported approach to design such materials, but suffers from several limitations, including in terms of mechanical properties. To improve peptide-based hydrogels interest and give rise to innovative properties, several strategies have been proposed in the recent years, and the development of multicomponent peptide-based hydrogels appears as a promising and relevant strategy. Indeed, mixing two or more compounds to develop new materials is a much-used approach that has proven its effectiveness in a wide variety of domains, including polymers, composites and alloys. While still limited to a handful of examples, we would like to report herein on the formulation and the comprehensive study of multicomponent hybrid DNA-nucleobase/peptide-based hydrogels using a multiscale approach based on a large panel of analytical techniques (i.e., rheometry, proton relaxometry, SAXS, electronic microscopy, infrared, circular dichroism, fluorescence, Thioflavin T assays). Among the six multicomponent systems studied, the results highlight the synergistic role of the presence of the two complementary DNA-nucleobases (i.e., adenine/thymine and guanine/cytosine) on the co-assembling process from structural (e.g., morphology of the nanoobjects) to physicochemical (e.g., kinetics of formation, fluorescence properties) and mechanical (e.g., stiffness, resistance to external stress) properties. All the data confirm the relevance of the multicomponent peptide-based approach in the design of innovative hydrogels and bring another brick in the wall of the understanding of these complex and promising systems.

摘要

基于肽的水凝胶是通过特定的超分子自组装过程形成的物理凝胶,导致有序的纳米结构,构成软物质的水捕获支架。由于肽的固有特性,这些水凝胶在生物医学领域受到高度关注,并在先进治疗和生物技术的应用方面开辟了新的视野。迄今为止,使用一种单一的天然肽来配制凝胶是设计此类材料最常报道的方法,但存在许多局限性,包括机械性能方面的局限性。为了提高基于肽的水凝胶的兴趣并赋予其创新性,近年来提出了几种策略,开发基于多组分的肽水凝胶似乎是一种很有前途和相关的策略。事实上,混合两种或两种以上的化合物来开发新材料是一种被广泛使用的方法,在包括聚合物、复合材料和合金在内的许多领域已经证明了其有效性。尽管仍然局限于少数几个例子,我们还是想在此报告使用基于多种分析技术的多尺度方法(即流变学、质子弛豫率、小角 X 射线散射、电子显微镜、红外、圆二色性、荧光、硫代黄素 T 测定)配制和全面研究基于多组分混合 DNA-碱基/肽的水凝胶。在所研究的六个多组分系统中,结果突出了两种互补 DNA-碱基(即腺嘌呤/胸腺嘧啶和鸟嘌呤/胞嘧啶)的存在对共组装过程的协同作用,从结构(例如纳米物体的形态)到物理化学(例如形成动力学、荧光性质)和机械(例如硬度、抵抗外部应力)性质。所有数据都证实了基于多组分肽的方法在设计创新水凝胶方面的相关性,并为这些复杂且有前途的系统的理解增添了另一个基石。

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