...
首页> 外文期刊>RSC Advances >Magnetic nanoparticles as double-edged swords: concentration-dependent ordering or disordering effects on lysozyme
【24h】

Magnetic nanoparticles as double-edged swords: concentration-dependent ordering or disordering effects on lysozyme

机译:磁性纳米颗粒作为双刃剑:对溶菌酶的浓度依赖性有序或无序效应

获取原文

摘要

The study of the interaction of nanoparticles (NPs) with proteins is of great importance due to its relevance in several fields including nano-biosafety, nano-bioscience, nano-biomedicine, and nano-biotechnology. However, the concentration dependency of NP–protein interactions and the effects on protein structure and function remain to be explored. Herein, we report the effect of concentration of iron oxide NPs, including Fe3O4 and Fe3O4 incorporated with arginine (Fe3O4@Arg), on the stability of hen egg white lysozyme (HEWL) (EC 3.2.1.1) used as a model protein. The NPs were synthesized and characterized using various methods, including Fourier transform infrared (FT-IR), transmission electron microscopy (TEM), scanning electron microscopy (SEM), vibrating sample magnetometer (VSM), dynamic light scattering (DLS), and X-ray diffraction (XRD). Subsequently, an attempt was made to explore the influence of the two types of NPs on the structure and stability of HEWL using fluorescence and circular dichroism (CD) spectroscopies. Moreover, functional stability analysis was performed by monitoring the remaining enzymatic activity of HEWL. Dual concentration dependent (DCD) effect of NPs on HEWL was observed, in which concentration threshold shift between two opposing effects, that is structure-making and structure-breaking, were determined to be 12.86 mg per μmol protein and 3.6 mg per μmol protein for Fe3O4 and Fe3O4@Arg, respectively. Kosmotropic-like and inversely chaotropic-like effects of NPs on HEWL are reported at lower and higher NPs/protein ratios, respectively. Accordingly, protein folding, helicity, and half-life were improved at a low concentration of NPs. The NPs act on HEWL structure and stability presumably through electrostatic adsorption on NPs, which, in turn, influences the structure and dynamics of the hydration water shell surrounding the protein molecules in the aqueous solution of HEWL. Therefore, NPs can act on HEWL either as a friend or foe depending on their concentration.
机译:纳米颗粒(NPs)与蛋白质相互作用的研究非常重要,因为它在包括纳米生物安全性,纳米生物科学,纳米生物医学和纳米生物技术在内的多个领域具有相关性。但是,NP-蛋白质相互作用的浓度依赖性以及对蛋白质结构和功能的影响仍有待探索。在此,我们报告了铁浓度较低的氧化铁NPs,包括Fe 3 O 4 和Fe 3 O 4 掺有精氨酸(Fe 3 O 4 @Arg),关于用作模型蛋白的鸡蛋清溶菌酶(HEWL)(EC 3.2.1.1)的稳定性。使用各种方法合成和表征NP,包括傅立叶变换红外(FT-IR),透射电子显微镜(TEM),扫描电子显微镜(SEM),振动样品磁力计(VSM),动态光散射(DLS)和X射线衍射(XRD)。随后,尝试使用荧光和圆二色性(CD)光谱法研究这两种NP对HEWL的结构和稳定性的影响。此外,通过监测HEWL的剩余酶活性进行功能稳定性分析。观察到NP对HEWL的双重浓度依赖性(DCD)作用,其中两个相对作用(即结构制造和结构破坏)之间的浓度阈值偏移确定为:每微摩尔蛋白为12.86 mg /μmol蛋白,对于每微摩尔蛋白为3.6 mg /μmol。 Fe 3 O 4 和Fe 3 O 4 @Arg。 NPs对HEWL的类似趋同性和反离液性的影响分别在较低和较高的NPs /蛋白质比率下报道。因此,在低浓度的NPs下,蛋白质折叠,螺旋度和半衰期得到改善。 NP大概通过对NP的静电吸附作用于HEWL的结构和稳定性,继而影响HEWL水溶液中蛋白质分子周围的水合水壳的结构和动力学。因此,NP可以根据自己的专注程度以朋友的身份或敌人的身份对HEWL起作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号