Characterization of Monoclonal Antibodies Generated against Norwalk virus Gil Capsid Protein Expressed in Escherichia coli

Mice, Inbred BALB C 0303 health sciences Immunoblotting Molecular Sequence Data Antibodies, Monoclonal Enzyme-Linked Immunosorbent Assay Antibodies, Viral 3. Good health Epitopes Feces Mice 03 medical and health sciences Capsid Escherichia coli Animals Humans Capsid Proteins Female Amino Acid Sequence Cloning, Molecular Antigens, Viral Epitope Mapping Caliciviridae Infections
DOI: 10.1111/j.1348-0421.2000.tb02582.x Publication Date: 2013-11-14T11:08:04Z
ABSTRACT
AbstractThe Norwalk virus (NV) causes outbreaks of acute non‐bacterial gastroenteritis in humans. The virus capsid is composed of a single 60 kDa protein. The capsid protein of NV36 (genogroup II, Mexico virus type) was expressed in an Escherichia coli system and ten monoclonal antibodies (MAbs) were generated against it. The reactivity of these MAbs was characterized using enzyme‐linked immunosorbent assay (ELISA) and Western blot (WB) analysis towards 20 overlapping fragments of the NV36 capsid protein expressed in E. coli. All of the MAbs recognized sequential (continuous) epitopes on the three antigenic regions. Six of the 10 MAbs recognized fragment 2 (equivalent residues 31–70), three MAbs recognized fragment 13 (residues 361–403) and one MAb recognized fragment 7 (residues 181–220), suggesting that the N‐terminal domain (residues 1–220) may contain more antigenic epitopes than the C‐terminal domain (residues 210–548). Furthermore, two MAbs (1B4 and 1F6) reacted in WB with three purified NV strains (genogroup II) derived from patients' stool samples. It was also found that genogroup I recombinant NV96–908 (genogroup I, KY89 type) could be detected as sensitively as recombinant NV36 (genogroup II) by ELISA with a set of the MAbs produced here.
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