RNA purification from Escherichia coli cells using boronated nanoparticles

被引:15
|
作者
Percin, Isik [1 ]
Idil, Neslihan [1 ]
Denizli, Adil [2 ]
机构
[1] Hacettepe Univ, Dept Biol, Ankara, Turkey
[2] Hacettepe Univ, Dept Chem, Ankara, Turkey
关键词
PHEMA; boronate affinity chromatography; Nanoparticles; RNA; VPBA; Escherichia coli; PERFORMANCE LIQUID-CHROMATOGRAPHY; ARGININE-AFFINITY CHROMATOGRAPHY; PLASMID DNA PURIFICATION; MAGNETIC NANOPARTICLES; EXTRACTION; SEPARATION; OLIGONUCLEOTIDES; RECOGNITION; ADSORPTION; COPOLYMER;
D O I
10.1016/j.colsurfb.2017.11.044
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Boronate affinity chromatography is a common purification method used for isolation and purification of cis-diol containing biomolecules. Poly (hydroxyethyl methacrylate-co-vinyl phenyl boronic acid) [P(HEMA-VPBA)] nanoparticles were prepared by miniemulsion polymerization to use in RNA purification methods. The P(HEMA-VPBA) nanoparticles were characterized by particle size distribution, surface area, Fourier transform infrared spectroscopy and atomic force microscopy. The effects of temperature, pH, RNA concentration and different salt types on RNA binding on the P(HEMA-VPBA) nanoparticles were examined. It was observed that RNA binding was increased with the increasing of pH and max RNA binding was obtained at pH 9.0. RNA binding capacity of the P(HEMA-VPBA) nanoparticles was increased from 167 mg/g to 601 mg/g with addition of BaCl2 to the binding medium. Maximum RNA binding capacity of the P(HEMA-VPBA) nanoparticles was 172 mg/g at 1.0 mg/mL initial RNA concentration. The P(HEMA-VPBA) nanoparticles were reusable for RNA binding. RNA was also extracted from Escherichia coli cells and purified successfully using the P(HEMA-VPBA) nanoparticles. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:146 / 153
页数:8
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