Target intelligence / Profile preview

Ebolavirus glycoprotein (specific to Zaire ebolavirus glycoprotein and Sudan ebolavirus glycoprotein) (GP (sometimes specified as GP(ZEBOV) for Zaire or GP(SEBOV) for Sudan))

Target
GP (sometimes specified as GP(ZEBOV) for Zaire or GP(SEBOV) for Sudan)
Molecular classification
Viral fusion glycoprotein, Envelope protein, Other (specific molecular family: Class I viral fusion protein)
01

Overview

Ebolavirus glycoprotein (GP) is the sole transmembrane glycoprotein on the surface of ebolavirus particles, including Zaire and Sudan species[1][2][3][4]. It is synthesized as a single precursor and cleaved into two subunits, GP1 (responsible for receptor binding) and GP2 (mediates membrane fusion), which assemble as a hetero-hexameric trimer on the virion surface[1][3]. The GP is highly glycosylated and forms a glycan shield that helps viruses evade the immune response[4][6]. GP mediates viral entry by attaching to host cell receptors and catalyzing the fusion of viral and cellular membranes—a process that requires proteolytic cleavage by host cathepsins and interactions with cellular lectins[1][6]. As the principal target for neutralizing antibodies, GP is the key antigen for vaccines, monoclonal antibody therapeutics, and entry inhibitors[1][2][4]. Differences in the structure and glycosylation of Zaire and Sudan ebolavirus GPs underlie significant variation in immune recognition and therapeutic efficacy, necessitating careful distinction in both research and medical applications[6]. If you later need structured information separately for “Zaire ebolavirus glycoprotein” and “Sudan ebolavirus glycoprotein”, they should each be treated as distinct canonical targets, though their properties are otherwise largely parallel except for sequence, immunogenicity, and some structural differences.

Other names
Ebolavirus envelope glycoproteinEbola GPGP1,2ZEBOV GP (for Zaire)SEBOV GP (for Sudan)Ebola virus glycoproteinSurface glycoprotein (sometimes “S” in literature, but not recommended)“GP” (most common abbreviation in research)
02

Mechanism of action

Neutralizing antibodies: Bind GP to block viral attachment or fusion, neutralizing infectivity[1][2][4]. Small-molecule inhibitors: Block GP processing (e.g., cathepsin inhibition) or interfere with conformational changes[1]. Vaccines: Use GP to elicit protective immune response

03

Biological functions

Viral attachment to host cellMembrane fusion (virus-host membrane)Mediating viral entry into host cellsImmune evasion (via glycan shield)Target for neutralizing antibodies
04

Disease associations

Infection (specifically Ebola virus disease)Other (primary pathogen virulence factor)
05

Safety considerations

Immune-mediated toxicity (antibody-dependent enhancement is a theoretical risk, though not conclusively shown for ebolaviruses)Mutational escape (antigenic drift can reduce drug/vaccine efficacy)Highly pathogenic target: vaccine trials and therapeutics need careful biosafety controls
06

Interacting drugs

Monoclonal antibodies (e.g., mAb114, REGN-EB3, ZMapp)

3 more in the full profile.

07

Biomarkers

Anti-GP antibody titers (for monitoring vaccine or therapeutic antibody efficacy)GP antigen detection (for diagnostic/monitoring active infection)

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