Cao Yu, Bai Gang, Chen Jiaqi, Tian Wang, Wang Shenqi, Yang Wenbo
Department of Microbiology, College of Life Sciences, Nankai University, Tianjin 300071, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Apr 3;833(2):236-44. doi: 10.1016/j.jchromb.2006.02.001. Epub 2006 Feb 21.
Magnetic agarose microspheres (MAMS), magnetic cellulose microspheres (MCMS), and magnetic poly(vinyl alcohol) microspheres (MPVAMS) were prepared by various different preparation methods. MCMS coupled with anti-IFN alpha-2b monoclonal antibodies (mAb) were selected for the purification of interferon alpha-2b (IFN alpha-2b) after performance characterization among microspheres. Parameters of immunomagnetic separation (IMS), including binding mAb, elution behavior, and sample pretreatment conditions, were optimized to improve the purification efficiency of the separation of IFN alpha-2b by MCMS. Size-exclusion HPLC (HPSEC) showed that the IFN alpha-2b was purified from crude cell lysate had an overall purity of 92.9%, while immunological and biological assays showed an activity recovery of 88.5% and specific antiviral activity of 2.7 x 10(8) IU/mg. Identity and molecular mass of purified IFN alpha-2b were confirmed by western blot and matrix-assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF-MS) analysis. This study illustrated the favorable separation media which combined desired properties for the development of magnetic separation of biological materials.
通过各种不同的制备方法制备了磁性琼脂糖微球(MAMS)、磁性纤维素微球(MCMS)和磁性聚乙烯醇微球(MPVAMS)。在对微球进行性能表征后,选择偶联有抗干扰素α-2b单克隆抗体(mAb)的MCMS用于纯化干扰素α-2b(IFNα-2b)。对免疫磁分离(IMS)的参数,包括结合单克隆抗体、洗脱行为和样品预处理条件进行了优化,以提高MCMS对IFNα-2b的分离纯化效率。尺寸排阻高效液相色谱(HPSEC)显示,从粗细胞裂解物中纯化得到的IFNα-2b总体纯度为92.9%,而免疫学和生物学测定显示活性回收率为88.5%,比抗病毒活性为2.7×10⁸IU/mg。通过蛋白质免疫印迹和基质辅助激光解吸电离飞行时间质谱(MALDI-TOF-MS)分析确认了纯化的IFNα-2b的同一性和分子量。本研究展示了一种优良的分离介质,其结合了生物材料磁性分离所需的特性。