Target intelligence / Profile preview

Haemagglutinin glycoprotein (influenza virus) (HA)

Target
HA
Molecular classification
Glycoprotein, Viral fusion protein (Class I fusion protein), Receptor-binding protein, Integral membrane protein
01

Overview

Haemagglutinin glycoprotein is a trimeric, integral membrane protein that projects from the surface of the influenza virus as spikes roughly 135 Å long. Each HA monomer is initially synthesized as the precursor HA0, which is proteolytically cleaved into HA1 (receptor binding) and HA2 (membrane fusion and anchor domains). The globular HA1 domain contains the receptor binding site, which recognizes terminal sialic acid residues on host cell surface glycoproteins. The HA2 subunit contains a fusion peptide that, upon exposure to acidic pH in endosomes, undergoes structural rearrangement to mediate viral and host membrane fusion. HA is highly antigenically variable, underpinning both seasonal influenza epidemics and pandemic outbreaks, and is a primary component of influenza vaccine formulations. Targeting the haemagglutinin glycoprotein with neutralizing antibodies or entry inhibitors is a cornerstone of influenza antiviral strategies.

Other names
HemagglutininInfluenza hemagglutininHA glycoprotein
02

Mechanism of action

Neutralizing antibody binding to globular head domain blocks receptor attachment and/or triggers immune clearance. Fusion inhibitors prevent conformational change necessary for membrane fusion.

03

Biological functions

Virus receptor binding (attachment to host cell sialic acid-containing receptors)Mediates endosomal membrane fusion (for viral entry)Antigenic determinant (major target for neutralizing antibodies and immune recognition)Erythrocyte agglutination (basis of diagnostic assays)
04

Disease associations

Infection (central to influenza virus infectivity)
05

Safety considerations

Antigenic drift and shift leading to immune escape and reduced vaccine efficacyRisk of severe allergic reactions to egg-produced HA in some vaccine settingsLimited cross-protection across distinct HA subtypesEnhanced pathogenicity with certain HA cleavage site mutations
06

Interacting drugs

Neuraminidase inhibitors (e.g., oseltamivir, zanamivir do not target HA directly, but interfere with related viral entry/exit processes)

2 more in the full profile.

07

Biomarkers

HA subtypes (e.g., H1, H3, H5) used for epidemiological typing and guiding vaccine strain selectionHA-specific antibody titers (e.g., hemagglutination inhibition assay in vaccine studies)

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