J Bacteriol Virol.  2011 Sep;41(3):183-187. 10.4167/jbv.2011.41.3.183.

Protein Expression of the Human Norovirus Capsid Gene using the Baculovirus Expression System

Affiliations
  • 1Department of Microbiology, College of Medicine, The Catholic University, Seoul, Korea. paik@catholic.ac.kr
  • 2Department of Dermatology, College of Medicine, The Catholic University, Seoul, Korea.
  • 3Department of Agricultural Biology, National Academy of Agricultural Science, Rural Development Association, Suwon, Korea.

Abstract

Human norovirus (HuNoV) is the major etiological agent of nonbacterial gastroenteritis worldwide. However, due to the absence of a rapid and sensitive diagnostic system, detection and monitoring have been limited. The HuNoV genome is composed of three open reading frames (ORFs). And major capsid protein, ORF2, is designated as a viral protein 1 (VP1). In this study, the baculovirus expression system was used for expression of the HuNoV capsid protein, VP1. Recombinant baculoviruses can be used as potent tools in HuNoV studies.

Keyword

Human norovirus; Baculovirus expression system

MeSH Terms

Baculoviridae
Capsid
Capsid Proteins
Gastroenteritis
Genome
Humans
Norovirus
Open Reading Frames
Capsid Proteins

Figure

  • Figure 1. Amplified Fragments of ORF2 S-P1 (543 bp), ORF2 epi (1,224 bp), and ORF2 P2 (347 bp) of the HuNoV capsid gene by RT-PCR (M: DNA size Marker).

  • Figure 2. The Gateway cloning strategy. The process comprises of two recombination processes; TOPO cloning reaction (A) and LR recombinant reaction (B).

  • Figure 3. Analysis of expression of recombinant protein from insect cells by SDS-PAGE; ORF2 epi (54 kDa), ORF2 S-P1 (29 kDa), and ORF2 P2 (23.4 kDa).


Cited by  1 articles

Protein Expression of the Bombyx mori Decapentaplegic Gene using the Baculovirus Expression Vector System
Seong Tae Jeong, Seung-Won Park
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