GIF (glycosylation-inhibiting factor) is a 13-kDa cytokine involved in immunosuppression by inhibiting N-glycosylation of IgE-binding factors (IgE-BF), thereby suppressing IgE synthesis . GIF antibodies are designed to detect and study the function of this cytokine in immune regulation.
GIF suppresses both IgE and IgG1 antibody responses by modulating T-cell priming and IgE-BF glycosylation . Mutated recombinant GIF derivatives (e.g., C57A/N106S) exhibit enhanced bioactivity compared to wild-type GIF:
| GIF Derivative | IgE Suppression (DNP-OVA Model) | IgG1 Suppression | Key Modification |
|---|---|---|---|
| Wild-type rhGIF | None | None | Native cysteine residues |
| C57A/N106S | Significant (p < 0.05) | Partial | Cys57 → Ala, Asn106 → Ser |
| C57A/N106S-CM | High (p < 0.01) | Significant | Additional carboxymethylation |
GIF antibodies enable precise detection of GIF expression in cellular and biochemical assays:
Detection:
Immunoprecipitation: Effective at 1:25–1:100 dilution.
Western Blot: Detects 13-kDa bands in human cell lysates.
Validation:
Flow Cytometry: Detects GIF on HeLa cells with FITC-conjugated secondaries.
Immunofluorescence: Cytoplasmic localization in fixed HeLa cells.
While not directly related to GIF antibodies, studies on IgG2 subclass engineering highlight strategies applicable to antibody design:
| Modification | Outcome |
|---|---|
| CH2 domain swaps | Reduced aggregation at low pH (e.g., IgG2_YLA variant) |
| FcRn binding | Altered biodistribution and catabolism (e.g., anti-gD antibodies) |
Nomenclature: The term "GIF2" is not standardized; it may refer to a specific isoform, mutant, or proprietary variant not yet published.
Therapeutic Potential: While GIF derivatives suppress IgE/IgG responses, clinical applications require optimization of bioavailability and safety .
Assay Optimization: Cross-reactivity and aggregation risks (observed in IgG2 antibodies ) necessitate careful conjugation and storage protocols .
KEGG: ath:AT1G01160
UniGene: At.11894