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一步法制备生物活性酶/无机材料。

One-step preparation of bioactive enzyme/inorganic materials.

机构信息

Department of Chemistry, University of Connecticut, U3060, Storrs, CT, 06269, USA.

Department of Molecular and Cell Biology, University of Connecticut, Storrs, CT, 06269, USA.

出版信息

J Mater Chem B. 2021 Oct 20;9(40):8451-8463. doi: 10.1039/d1tb01652k.

Abstract

Simultaneous exfoliation of crystalline α-zirconium phosphate (α-ZrP) nanosheets and enzyme binding, induced by shearing, without the addition of any toxic additives is reported here for the first time. These materials were thoroughly characterized and used for applications. The bulk α-ZrP material (20 mg mL) was exfoliated with low concentrations of a protein such as bovine serum albumin (BSA, 3 mg mL) in a shear reactor at 10k rpm for <80 minutes. Exfoliation was monitored by powder X-ray diffraction with samples displaying a gradual but complete loss of the 7.6 Å (002) peak, which is characteristic of bulk α-ZrP. The fully exfoliated sample loaded with the protein was characterized by transmission and scanning electron microscopy in addition to other biophysical methods. Lysozyme, glucose oxidase, met-hemoglobin, and ovalbumin also induced exfoliation and directly produced enzyme/ZrP biocatalysts. Thus, exfoliation, biophilization and enzyme binding are accomplished in a single step. Several factors contributed to the exfoliation kinetics, and the rate increased with α-ZrP and BSA concentrations and decreased with pH. However, the exfoliation efficiency inversely depended on the isoelectric point of the protein with ovalbumin (pI = 4.5) being the best and lysozyme (pI = 11.1) being the worst. A strong correlation between the protein size and exfoliation efficiency was noted, and the latter suggests the role of hydrodynamic factors in the process. Exfoliation was also achieved by simple stirring using a magnetic stirrer, under low volumes, and model enzymes, indicating 60-90% retention of bound enzymatic activities. The addition of BSA to enzymes as the diluent and stabilizing agent also prevents enzymes from the denaturing effect caused by stirring. This new method requires no pre-treatment of α-ZrP with toxic exfoliating agents such as tetrabutyl ammonium hydroxide and provides bioactive enzyme/inorganic materials in a single step. These protein-loaded biocompatible nanosheets may be useful for biocatalysis and biomedical applications.

摘要

本文首次报道了在不添加任何有毒添加剂的情况下,通过剪切同时实现结晶α-磷酸锆(α-ZrP)纳米片的剥离和酶结合。这些材料进行了彻底的表征并用于应用。在剪切反应器中,以 10k rpm 的速度在低浓度的蛋白质(如牛血清白蛋白(BSA),3mg/mL)存在下,将块状α-ZrP 材料(20mg/mL)剥离 80 分钟以内。通过粉末 X 射线衍射监测剥离情况,样品显示出逐渐但完全失去了 7.6Å(002)峰的特征,这是块状α-ZrP 的特征。用蛋白质负载的完全剥离的样品通过透射和扫描电子显微镜以及其他生物物理方法进行了表征。溶菌酶、葡萄糖氧化酶、高铁血红蛋白和卵清蛋白也诱导了剥离,并直接产生了酶/ZrP 生物催化剂。因此,剥离、生物矿化和酶结合在一个步骤中完成。几个因素促成了剥离动力学,随着α-ZrP 和 BSA 浓度的增加以及 pH 值的降低,速率增加。然而,剥离效率与蛋白质的等电点呈反比,其中卵清蛋白(pI=4.5)效果最好,溶菌酶(pI=11.1)效果最差。还注意到蛋白质大小与剥离效率之间存在很强的相关性,后者表明在该过程中流体动力因素的作用。通过在低体积下使用磁力搅拌器进行简单搅拌也可以实现剥离,并且模型酶的保留了 60-90%的结合酶活性。在酶中添加 BSA 作为稀释剂和稳定剂也可以防止酶因搅拌而变性。这种新方法不需要用有毒的剥离剂(如四丁基氢氧化铵)对α-ZrP 进行预处理,并且可以在一个步骤中提供生物活性酶/无机材料。这些负载蛋白质的生物相容性纳米片可用于生物催化和生物医学应用。

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