GONUTS has been updated to MW1.31 Most things seem to be working but be sure to report problems.

Have any questions? Please email us at ecoliwiki@gmail.com


Jump to: navigation, search

Pearce, LA, Yu, M, Waddington, LJ, Barr, JA, Scoble, JA, Crameri, GS and McKinstry, WJ (2015) Structural characterization by transmission electron microscopy and immunoreactivity of recombinant Hendra virus nucleocapsid protein expressed and purified from Escherichia coli. Protein Expr. Purif. 116:19-29


Hendra virus (family Paramyxoviridae) is a negative sense single-stranded RNA virus (NSRV) which has been found to cause disease in humans, horses, and experimentally in other animals, e.g. pigs and cats. Pteropid bats commonly known as flying foxes have been identified as the natural host reservoir. The Hendra virus nucleocapsid protein (HeV N) represents the most abundant viral protein produced by the host cell, and is highly immunogenic with naturally infected humans and horses producing specific antibodies towards this protein. The purpose of this study was to express and purify soluble, functionally active recombinant HeV N, suitable for use as an immunodiagnostic reagent to detect antibodies against HeV. We expressed both full-length HeV N, (HeV NFL), and a C-terminal truncated form, (HeV NCORE), using a bacterial heterologous expression system. Both HeV N constructs were engineered with an N-terminal Hisx6 tag, and purified using a combination of immobilized metal affinity chromatography (IMAC) and size exclusion chromatography (SEC). Purified recombinant HeV N proteins self-assembled into soluble higher order oligomers as determined by SEC and negative-stain transmission electron microscopy. Both HeV N proteins were highly immuno-reactive with sera from animals and humans infected with either HeV or the closely related Nipah virus (NiV), but displayed no immuno-reactivity towards sera from animals infected with a non-pathogenic paramyxovirus (CedPV), or animals receiving Equivac® (HeV G glycoprotein subunit vaccine), using a Luminex-based multiplexed microsphere assay.


PubMed Online version:10.1016/j.pep.2015.07.008


Amino Acid Sequence; Animals; Antibodies, Viral/immunology; Cloning, Molecular; Escherichia coli/genetics; Gene Expression; Hendra Virus/chemistry; Hendra Virus/genetics; Hendra Virus/immunology; Hendra Virus/ultrastructure; Henipavirus Infections/immunology; Henipavirus Infections/virology; Horses; Humans; Molecular Sequence Data; Nucleocapsid Proteins/chemistry; Nucleocapsid Proteins/genetics; Nucleocapsid Proteins/immunology; Nucleocapsid Proteins/ultrastructure; Plasmids/genetics; Recombinant Proteins/chemistry; Recombinant Proteins/genetics; Recombinant Proteins/immunology; Recombinant Proteins/ultrastructure; Swine



Gene product Qualifier GO Term Evidence Code with/from Aspect Extension Notes Status


GO:0005198: structural molecule activity



Figure 2 shows the comparison of the Western blots of Hendra virus nucleocapsid protein/HeV N/nucleocapsid wild type and a mutant in Henipavirus Hendra to show its presence within the virion.

CACAO 13348


See also


See Help:References for how to manage references in GONUTS.