| Literature DB >> 25957800 |
Hao Li1, Yanli Yang1, Yan Zhang2, Songping Zhang2, Qizu Zhao3, Yuanyuan Zhu3, Xingqi Zou3, Mengran Yu1, Guanghui Ma2, Zhiguo Su4.
Abstract
A purification scheme based on hydrophobic interaction chromatography was developed to separate inactivated foot-and-mouth disease virus (FMDV) from crude supernatant. About 92% recovery and 8.8-fold purification were achieved on Butyl Sepharose 4 FF. Further purification on Superdex 200 resulted in another 29-fold purification, with 92% recovery. The columns were coupled through an intermediate ultrafiltration unit to concentrate the virus. The entire process was completed in about 3.5h, with 75% final FMDV recovery, and 247-fold purification. The final product had purity above 98%, with over 99.5% of host cell DNA removed. High-performance size exclusion chromatography (HPSEC), Western blot, dynamic light scattering (DLS), and transmission electron microscopy (TEM) indicated that the purified virus contained the required antigen, and was structurally intact with a spherical shape and a particle size of 28 nm.Entities:
Keywords: Downstream processing; Foot-and-mouth disease virus; Hydrophobic interaction chromatography; Purification
Mesh:
Year: 2015 PMID: 25957800 DOI: 10.1016/j.pep.2015.04.011
Source DB: PubMed Journal: Protein Expr Purif ISSN: 1046-5928 Impact factor: 1.650