FUT3 antibody is a research tool used to detect and study the enzyme fucosyltransferase 3 (FUT3), a key player in the biosynthesis of Lewis blood group antigens. FUT3 catalyzes the addition of fucose to glycosphingolipids, generating antigens such as Lewis a (Leᵃ), Lewis b (Leᵇ), and sialyl Lewis x (sLeˣ), which are critical for cellular adhesion, inflammation, and tumor metastasis . These antibodies are indispensable in investigating FUT3’s role in diseases like cancer, where its overexpression correlates with aggressive phenotypes and poor prognosis .
FUT3 is a glycosyltransferase with α(1,3)- and α(1,4)-fucosyltransferase activities, enabling it to modify glycans on cell surfaces and secreted glycoproteins. Its protein structure includes a catalytic domain and a transmembrane segment that anchors it to the Golgi apparatus . Key features include:
Tissue Expression: Highly expressed in exocrine epithelial cells, stomach, colon, intestine, lung, and kidney .
FUT3 antibodies vary in clonality, epitope specificity, and applications. Below is a comparative analysis of prominent antibodies:
Note: WB = Western blot; IHC = Immunohistochemistry; IF = Immunofluorescence.
FUT3 antibodies are employed in diverse experimental contexts:
Glycan Synthesis: FUT3 generates sLeˣ and sLeᵃ, ligands for E-selectin, facilitating cancer cell adhesion to endothelial cells .
Metabolic Reprogramming: In LUAD, FUT3 knockdown inhibits glycolysis, reducing ATP production and tumor progression .
Clear Cell Renal Cell Carcinoma (ccRCC): FUT3 expression improves OS and RFS prediction when combined with the Leibovich model (C-index improved from 0.829 to 0.854) .
Pancreatic Cancer: Tumorigenicity in xenograft models is nearly abolished with FUT3 knockdown (tumor volume ↓98%) .
FUT3 antibodies are pivotal in: