Target intelligence / Profile preview

Feline infectious peritonitis virus membrane protein (M protein) (M protein)

Target
M protein
Molecular classification
Viral structural protein, Membrane protein, Glycoprotein
01

Overview

The Feline infectious peritonitis virus (FIPV) membrane protein, historically referred to as the small integral membrane glycoprotein, is the most abundant structural protein of the viral envelope [1, 4]. It is a triple-spanning membrane protein that plays a central role in virion morphogenesis by coordinating the assembly of other structural proteins, including the Spike (S), Envelope (E), and Nucleocapsid (N) proteins [7, 11]. In the pathogenesis of FIP, the M protein is a key immunological target; monoclonal antibodies like FK50-4 have been demonstrated to neutralize the virus and prevent infection in feline macrophages, the primary host cells for FIPV [1]. Unlike the Spike protein, which is often implicated in antibody-dependent enhancement (ADE), the M protein contains conserved epitopes that are candidates for safer vaccine designs and therapeutic antibodies [2, 8]. While research into small-molecule inhibitors for the M protein is ongoing, it remains a critical target for disrupting the viral life cycle and preventing the fatal progression of feline infectious peritonitis [4, 16].

Other names
Small integral membrane glycoproteinMembrane glycoproteinMatrix proteinE1 proteinFeline coronavirus membrane protein
02

Mechanism of action

Neutralization of viral entry and replication; interference with virion assembly and budding.

03

Biological functions

Viral assemblyViral buddingVirion morphogenesisHost-virus interaction
04

Disease associations

InfectionFeline infectious peritonitis
05

Safety considerations

Antibody-dependent enhancement (ADE)Therapeutic challenges due to viral mutation
06

Interacting drugs

Monoclonal antibody FK50-4

1 more in the full profile.

07

Biomarkers

Anti-M protein antibodies

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