alpha-Glucuronosyl and alpha-glucosyl diacylglycerides, natural killer T cell-activating lipids from bacteria and fungi
AuthorBurugupalli, S; Almeida, CF; Smith, DGM; Shah, S; Patel, O; Rossjohn, J; Uldrich, AP; Godfrey, DI; Williams, SJ
Source TitleChemical Science
PublisherROYAL SOC CHEMISTRY
University of Melbourne Author/sWilliams, Spencer; Godfrey, Dale; Rossjohn, Jamie; Uldrich, Adam; Patel, Onisha; Dos Santos Sa E Almeida, Catarina; Shah, Sayali; Burugupalli, Satvika
AffiliationMicrobiology and Immunology
School of Chemistry
Medical Biology (W.E.H.I.)
Document TypeJournal Article
CitationsBurugupalli, S., Almeida, C. F., Smith, D. G. M., Shah, S., Patel, O., Rossjohn, J., Uldrich, A. P., Godfrey, D. I. & Williams, S. J. (2020). alpha-Glucuronosyl and alpha-glucosyl diacylglycerides, natural killer T cell-activating lipids from bacteria and fungi. CHEMICAL SCIENCE, 11 (8), pp.2161-2168. https://doi.org/10.1039/c9sc05248h.
Access StatusOpen Access
NHMRC Grant codeNHMRC/1016629
ARC Grant codeARC/FT140100278
Natural killer T cells express T cell receptors (TCRs) that recognize glycolipid antigens in association with the antigen-presenting molecule CD1d. Here, we report the concise chemical synthesis of a range of saturated and unsaturated α-glucosyl and α-glucuronosyl diacylglycerides of bacterial and fungal origins from allyl α-glucoside with Jacobsen kinetic resolution as a key step. These glycolipids are recognized by a classical type I NKT TCR that uses an invariant Vα14-Jα18 TCR α-chain, but also by an atypical NKT TCR that uses a different TCR α-chain (Vα10-Jα50). In both cases, recognition is sensitive to the lipid fine structure, and includes recognition of glycosyl diacylglycerides bearing branched (R- and S-tuberculostearic acid) and unsaturated (oleic and vaccenic) acids. The TCR footprints on CD1d loaded with a mycobacterial α-glucuronosyl diacylglyceride were assessed using mutant CD1d molecules and, while similar to that for α-GalCer recognition by a type I NKT TCR, were more sensitive to mutations when α-glucuronosyl diacylglyceride was the antigen. In summary, we provide an efficient approach for synthesis of a broad class of bacterial and fungal α-glycosyl diacylglyceride antigens and demonstrate that they can be recognised by TCRs derived from type I and atypical NKT cells.
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