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重组蜘蛛丝蛋白的水相静电纺丝。

Aqueous electrospinning of recombinant spider silk proteins.

机构信息

University of Bayreuth, Dept. of Biomaterials, Prof.-Rüdiger-Bormann-Str. 1, 95447 Bayreuth, Germany.

University of Bayreuth, Biopolymer Processing Group, Ludwig-Thomas-Str. 36a, 95447 Bayreuth, Germany.

出版信息

Mater Sci Eng C Mater Biol Appl. 2020 Jan;106:110145. doi: 10.1016/j.msec.2019.110145. Epub 2019 Aug 29.

Abstract

There has been a significant increase in the use of sensitive biological components, e.g., growth factors or enzymes, in implanted scaffolds/devices. To prevent diffusion away from the targeted area and to maximize access of the biological agent to the desired target, it is necessary to provide a supportive substrate to immobilize and protect biological agents from the environment. For this purpose, nanofiber fabrics are highly promising due to their high porosity, capacity for solution flow-through and high surface-to-volume ratio. However, electrospinning often requires harsh processing conditions, such as the use of volatile solutions, which can result in loss of activity of the incorporated biological components. In this study we developed a mild process for electrospinning of eADF4(C16), a recombinant spider silk protein. eADF4(C16) is non-cytotoxic, displays excellent stability against hydrolytic and enzymatic degradation and opens the opportunity for genetic addition of bioactive factors. Therefore, an aqueous spinning dope of eADF4(C16) was loaded with either green fluorescence protein (GFP) or the recombinant fusion protein GFP-eADF4(C16). The fluorescence activity of GFP is dependent on its proper folding, which does not occur in organic solvents, making it an attractive model protein. We were able to demonstrate the usability as well as the significance of the all-aqueous processing conditions for the activity of GFP in electrospun spider silk scaffolds.

摘要

在植入式支架/器械中,越来越多地使用敏感的生物成分,例如生长因子或酶。为了防止从目标区域扩散,并使生物制剂最大限度地到达所需的靶标,有必要提供一个支持性的基质来固定和保护生物制剂免受环境影响。为此,纳米纤维织物因其高孔隙率、溶液可流通能力和高表面积与体积比而具有很大的应用前景。然而,静电纺丝通常需要苛刻的加工条件,例如使用挥发性溶液,这可能导致掺入的生物成分的活性丧失。在这项研究中,我们开发了一种温和的电纺工艺来制备重组蜘蛛丝蛋白 eADF4(C16)。eADF4(C16)无细胞毒性,对水解和酶降解具有极好的稳定性,并为遗传添加生物活性因子提供了机会。因此,将 eADF4(C16)的水性纺丝溶液加载到绿色荧光蛋白 (GFP) 或 GFP-eADF4(C16) 的重组融合蛋白中。GFP 的荧光活性依赖于其正确的折叠,而这在有机溶剂中是不会发生的,因此 GFP 是一种很有吸引力的模型蛋白。我们能够证明在电纺蜘蛛丝支架中,全水加工条件对 GFP 活性的可用性和重要性。

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