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IMX313 domain (IMX313)

Target
IMX313
Molecular classification
Other (protein oligomerization domain, not a classical biological target such as receptor, enzyme, ion channel, or transporter)
01

Overview

The **IMX313 domain** is a synthetic, engineered 55-amino-acid protein domain derived as a hybrid from the oligomerization domains of chicken complement inhibitor C4b-binding protein (C4bp), which shares approximately 21% homology with the human analogue. Its primary function is to **self-assemble into stable heptameric (seven-unit) nanoparticles** when fused genetically to an antigen, resulting in increased immunogenicity of the fused antigen by promoting higher-order multimerization. This multimerization has been shown to significantly enhance antibody and sometimes T-cell responses to the antigen, improving vaccine efficacy in preclinical and early clinical studies, particularly for malaria (e.g. *Plasmodium falciparum* Pfs25-IMX313) and tuberculosis (e.g. Ag85A-IMX313) vaccines. IMX313 itself does not function as a direct biological target (such as a receptor or enzyme) but rather serves as a molecular scaffold for antigen display in novel vaccine constructs[1][2][3][4][5][6]. IMX313 is not an endogenous protein, nor is it listed as a validated therapeutic target for drug discovery, and is instead a biotechnological tool for immunogen design[2][3][4]. Fusion of antigens to IMX313 is required for its adjuvant-like properties; mixing IMX313 as a separate protein with an antigen does not produce the same effect[5]. Early-phase clinical trials have shown favorable safety and immunogenicity, with no significant immune reactivity to the human homolog detected[2][3]. IMX313 is not associated with small-molecule drugs and does not itself serve as a biomarker; safety concerns are specific to the context of the antigen to which it is fused and to the theoretical risk of breaking immunological tolerance to self-proteins. Summary: - IMX313 is a synthetic oligomerization domain used to assemble antigens into higher-order structures, acting as a vaccine immunogenicity enhancer by multivalency, but is not a molecular therapeutic target in the conventional sense. - It is most accurately classified as an engineered protein domain used as a vaccine design tool. - Not applicable for lists of canonical "therapeutic targets," drug interactions, biomarkers, or mechanism-of-action in isolation. If structured fields are required for a molecule that is a genuine therapeutic target (e.g., receptor, enzyme), IMX313 does not qualify; record this entry as non-target/informational and flag as "is_incorrect: true" for this reason[2][3][4][5][6].

Other names
Hybrid chicken C4b-binding protein oligomerization domainC4bp oligomerization domainC4bp (IMX313 variant) domain
02

Biological functions

Antigen multimerizationImmune response enhancement (when fused to antigens)
03

Disease associations

Other (adjuvant use in infectious disease vaccines, e.g. malaria, tuberculosis)
04

Safety considerations

Potential induction of anti-self immune response (immunogenicity against human C4bp theoretically possible, but not observed in clinical trials)General immunogenicity profile to be evaluated case-by-case in vaccine context[2][3]

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