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单壁碳纳米管对静电纺丝牛血清白蛋白/聚乙烯醇膜酯水解和形貌的作用。

Role of single-walled carbon nanotubes on ester hydrolysis and topography of electrospun bovine serum albumin/poly(vinyl alcohol) membranes.

机构信息

Molecular Sciences and Engineering Team, Natick Soldier Research, Development and Engineering Center , Natick, Massachusetts 01760, United States.

出版信息

ACS Appl Mater Interfaces. 2014 Jul 23;6(14):11741-8. doi: 10.1021/am502495e. Epub 2014 Jul 14.

Abstract

Electrospun membranes were studied for the chemical deactivation of threat agents by means of enzymatic proteins. Protein loading and the surface chemistry of hybrid nanofibers influenced the efficacy by which embedded enzymes could digest the substrate of interest. Bovine serum albumin (BSA), selected as a model protein, was electrospun into biologically active fibers of poly(vinyl alcohol), PVA. Single-walled carbon nanotubes (SWNTs) were blended within these mixtures to promote protein assembly during the process of electrospinning and subsequently the ester hydrolysis of the substrates. The SWNT incorporation was shown to influence the topography of PVA/BSA nanofibers and enzymatic activity against paraoxon, a simulant for organophosphate agents and a phosphorus analogue of p-nitrophenyl acetate (PNA). The esterase activity of BSA against PNA was uncompromised upon its inclusion within nanofibrous membranes because similar amounts of PNA were hydrolyzed by BSA in solution and the electrospun BSA. However, the availability of BSA along the fiber surface was shown to affect the ester hydrolysis of paraoxon. Atomic force microscopy images of nanofibers implicated the surface migration of BSA during the electrospinning of SWNT filled dispersions, especially as greater weight fractions of protein were added to the spinning mixtures. In turn, the PVA/SWNT/BSA nanofibers outperformed the nanotube free PVA/BSA membranes in terms of paraoxon digestion. The results support the development of electrospun polymer nanofiber platforms, modulated by SWNTs for enzyme catalytic applications relevant to soldier protective ensembles.

摘要

静电纺丝膜被研究用于通过酶蛋白对威胁剂进行化学失活。蛋白质负载和混合纳米纤维的表面化学影响了嵌入酶消化感兴趣的底物的功效。牛血清白蛋白(BSA)被选为模型蛋白,被电纺成具有生物活性的聚乙烯醇(PVA)纤维。单壁碳纳米管(SWNTs)被混入这些混合物中,以促进电纺过程中蛋白质的组装,随后对底物进行酯水解。SWNT 的掺入被证明会影响 PVA/BSA 纳米纤维的形貌和对马拉硫磷的酶活性,马拉硫磷是有机磷剂的模拟物,也是对硝基苯基乙酸酯(PNA)的磷类似物。BSA 对 PNA 的酯酶活性在其包含在纳米纤维膜中时并未受到影响,因为在溶液中和电纺的 BSA 中水解了相似量的 PNA。然而,BSA 在纤维表面的可用性被证明会影响马拉硫磷的酯水解。纳米纤维的原子力显微镜图像表明,在填充有 SWNT 的分散体的电纺过程中,BSA 会发生表面迁移,尤其是当向纺丝混合物中添加更多重量分数的蛋白质时。反过来,与不含纳米管的 PVA/BSA 膜相比,PVA/SWNT/BSA 纳米纤维在马拉硫磷消化方面表现更好。结果支持了静电纺丝聚合物纳米纤维平台的发展,该平台通过 SWNT 进行调制,用于与士兵防护装备相关的酶催化应用。

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