Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 May;63(3):362-70.
doi: 10.1002/bab.1379. Epub 2015 Jul 6.

Expression and characterization of hepatitis E virus-like particles and non-virus-like particles from insect cells

Affiliations
Review

Expression and characterization of hepatitis E virus-like particles and non-virus-like particles from insect cells

Ying Qi et al. Biotechnol Appl Biochem. 2016 May.

Abstract

The hepatitis E virus (HEV) capsid antigen expressed in insect cell has been proposed as a candidate subunit vaccine for the prevention of hepatitis E. However, the expression and purification of HEV virus-like particles (VLPs) from insect cells have not been explored. We aimed to optimize the procedure to obtain HEV VLPs. In this study, two conformations of the HEV capsid proteins were expressed in insect cells, VLPs and non-VLPs, and they were purified separately. The physicochemical properties and the humoral immune responses induced by the two forms were analyzed and compared. We found that HEV VLPs were more immunogenic in mice than HEV non-VLPs. Therefore, we optimized the conditions that yielded high VLPs expression in insect cell cultures and developed an efficient purification method. The results suggest that the distinction and isolation of VLPs from non-VLPs are essential to generate a more immunogenic vaccine.

Keywords: capsid protein; hepatitis E virus; non-virus-like particle; particle assembly; virus-like particles.

PubMed Disclaimer

Similar articles

Cited by

Substances

LinkOut - more resources