A NS1-binding monoclonal antibody interacts with two residues that are highly conserved in seasonal as well as newly emerged influenza A virus

Autor: Chee-Keng Mok, Su Hui Catherine Teo, Yee-Joo Tan, Jianping Wu
Rok vydání: 2018
Předmět:
Microbiology (medical)
Nucleolus
medicine.drug_class
Intracellular localization
viruses
Fluorescent Antibody Technique
Cross Reactions
Viral Nonstructural Proteins
medicine.disease_cause
Monoclonal antibody
Antibodies
Viral

Cell Line
non-structural protein 1 (NS1)
03 medical and health sciences
Epitopes
Structure-Activity Relationship
Influenza
Human

Influenza A virus
medicine
Immunology and Allergy
Animals
Humans
Amino Acids
Conserved Sequence
030304 developmental biology
0303 health sciences
Binding Sites
General Immunology and Microbiology
030306 microbiology
Effector
Chemistry
monoclonal antibody 19H9
virus diseases
Antibodies
Monoclonal

General Medicine
Influenza A virus subtype H5N1
Cell biology
Infectious Diseases
Epitope mapping
Cytoplasm
Epitope Mapping
Protein Binding
Research Article
Zdroj: Pathogens and Disease
ISSN: 2049-632X
Popis: The non-structural protein 1 (NS1) of influenza A virus (IAV) is a multifunctional protein that antagonizes host antiviral responses, modulating virus pathogenesis. As such, it serves as a good target for research and diagnostic assay development. In this study, we have generated a novel monoclonal antibody (mAb) 19H9 and epitope mapping revealed that two residues, P85 and Y89, of NS1 are essential for interacting with this mAb. Furthermore, residues P85 and Y89 are found to be highly conserved across different IAV subtypes, namely seasonal H1N1 and H3N2, as well as the highly pathogenic H5N1 and H5N6 avian strains. Indeed, mAb 19H9 exhibits broad cross-reactivity with IAV strains of different subtypes. The binding of mAb 19H9 to residue Y89 was further confirmed by the abrogation of interaction between NS1 and p85β. Additionally, mAb 19H9 also detected NS1 proteins expressed in IAV-infected cells, showing NS1 intracellular localization in the cytoplasm and nucleolus. To our knowledge, mAb 19H9 is the first murine mAb to bind at the juxtaposition between the N-terminal RNA-binding domain and C-terminal effector domain of NS1. It could serve as a useful research tool for studying the conformational plasticity and dynamic changes in NS1.
Generation and characterization of a novel monoclonal antibody which binds to two highly conserved residues in NS1 of influenza A virus.
Databáze: OpenAIRE