5kxc
From Proteopedia
Wisteria floribunda lectin in complex with GalNAc(beta1-4)GlcNAc (LacdiNAc) at pH 8.5.
Structural highlights
FunctionPublication Abstract from PubMedAberrant glycosylation and the overexpression of specific carbohydrate epitopes is a hallmark of many cancers, and tumor-associated oligo-saccharides are actively investigated as targets for immunotherapy and diagnostics. Wisteria floribunda agglutinin (WFA) is a legume lectin that recognizes terminal N-acetylgalactosaminides with high affinity. WFA preferentially binds the disaccharide LacdiNAc (beta-D-GalNAc-[1-->4]-D-GlcNAc), which is associated with tumor malignancy in leukemia, prostate, pancreatic, ovarian, and liver cancers, and has shown promise in cancer glycobiomarker detection. The mechanism of specificity for WFA recognition of LacdiNAc is not fully understood. To address this problem, we have determined affinities and structure of WFA in complex with GalNAc and LacdiNAc. Affinities towards Gal, GalNAc, and LacdiNAc were measured via surface plasmon resonance, yielding KD values of 4.67 x 10-4 M, 9.24 x 10-5 M, and 5.45 x 10-6 M respectively. Structures of WFA in complex with LacdiNAc and GalNAc have been determined to 1.80 A - 2.32 A resolution. These high-resolution structures revealed a hydrophobic groove complementary to the GalNAc and, to a minor extent, to the backface of the GlcNAc sugar ring. Remarkably, the contribution of this small hydrophobic surface significantly increases the observed affinity for LacdiNAc over GalNAc. Tandem MS sequencing confirmed presence of two isolectin forms in commercially available WFA differing only in the identities of two amino acids. Finally, the WFA carbohydrate binding site is similar to a homologous lectin isolated from Vatairea macrocarpa in complex with GalNAc which, unlike WFA, binds not only alphaGalNAc but also terminal Ser/Thr O-linked alphaGalNAc (Tn antigen). Molecular basis for recognition of the cancer glycobiomarker LacdiNAc (GalNAc(beta1-4)GlcNAc) by Wisteria floribunda agglutinin.,Haji-Ghassemi O, Gilbert M, Spence J, Schur MJ, Parker MJ, Jenkins ML, Burke JE, van Faassen H, Young NM, Evans SV J Biol Chem. 2016 Sep 6. pii: jbc.M116.750463. PMID:27601469[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. Loading citation details.. Citations No citations found See AlsoReferences
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