Assembly of the capsid protein of red-spotted grouper nervous necrosis virus during purification, and role of calcium ions in chromatography

• Published in: Biotechnology and bioprocess engineering Vol. 21; no. 3; pp. 373 - 380
• Main Authors: Kim, Hyoung Jin, Kwag, Hye-Lim, Kim, Do Gyun, Kang, Bo Kyu, Han, Sang Yoon, Moon, Hyoungjoon, Hwang, Jee Youn, Kwon, Mun-Gyeong, Kang, Hyun Ah, Kim, Hong-Jin
• Format: Journal Article
• Language: English
• Published: Seoul The Korean Society for Biotechnology and Bioengineering 01.06.2016; Springer Nature B.V; 한국생물공학회
• Subjects: Analysis; Animal vaccines; Antigens; Aquaculture; Biotechnology; Calcium; Chemistry; Chemistry and Materials Science; Chromatography; coat proteins; farmed fish; financial economics; Fish; Fish diseases; fish industry; Genetic recombination; Glycerol; grouper; Hemodialysis; heparin; Hepatitis B; Human papillomavirus; Industrial and Production Engineering; Ions; Pathogens; Proteins; purification methods; R&D; Redspotted grouper nervous necrosis virus; Research & development; Research Paper; Sample preparation; Studies; Vaccines; virus-like particles; Viruses; 생물공학; assembly; virus-like particles; heparin chromatography; calcium ion; nervous necrosis virus
• ISSN: 1226-8372; 1976-3816
• DOI: 10.1007/s12257-016-0256-8

Currently virus-like particles (VLPs) are receiving much attention as platforms for next generation vaccines. However, chromatography-based methods for purifying VLPs remain challenging. Unlike traditional methods using density gradient for purifying VLPs, there have been few advances in explaining how assembled particles can be obtained by chromatography. Nervous necrosis virus (NNV) infects over 30 species of fish and leads to large economic losses in the farmed fish industry. Previously we developed a heparin chromatography-based method for purifying red-spotted grouper NNV (RGNNV) VLPs. However it is unclear how the assembled RGNNV VLPs are obtained by this method. It is known that assembly of NNV capsid proteins depends on calcium ions. In the present study, we found that the yield of purified RGNNV capsid protein in heparin chromatography was enhanced when calcium ions were present during binding. Also, it appears that the capsid protein of RGNNV undergoes partial disassembly and reassembly during sample preparation prior to heparin chromatography and the protein finally undergoes assembly during the chromatography. Therefore, our results indicated that heparin-binding affinity of RGNNV capsid protein is linked to its ability for VLP formation. The assembly of RGNNV capsid proteins recombinantly produced is a good model for explaining VLP formation during chromatography-based purification processes.