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Virus surface proteins refer collectively to a diverse group of structural and functional proteins situated on the exterior of viruses, including glycoproteins, envelope proteins, fusion proteins, and spike proteins[3][4][9]. These proteins mediate essential steps in the viral life cycle, primarily enabling attachment to and entry into host cells by binding to specific cellular receptors and/or mediating membrane fusion[3][4][6][7]. Major classes of viral surface proteins include class I, II, III, and IV fusion proteins, differing in structure and mechanism but sharing the role of driving entry into host cells[3][4][7]. Virus surface proteins are frequent targets for antiviral drug development and neutralizing antibodies in vaccines[3][4]. The term "virus surface proteins" does not specify a single molecule, but rather encompasses a heterogeneous family of proteins with varied sequence, structure, and function across different virus taxa, such as the spike (S) protein of coronaviruses, hemagglutinin (HA) of influenza, gp120/gp41 of HIV, and glycoprotein (GP) of filoviruses.
Inhibition of viral entry, Blockade of receptor binding, Disruption of membrane fusion
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