7MXH

CD1c with antigen analogue 3

7MXH の概要

• エントリーDOI: 10.2210/pdb7mxh/pdb
• 分子名称: T-cell surface glycoprotein CD1c/T-cell surface glycoprotein CD1b chimeric protein, Beta-2-microglobulin, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (8 entities in total)
• 機能のキーワード: lipid, cd1c, antigen-presenting, tuberculosis, lipid binding protein, immune system
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 46247.04

構造登録者

Cao, T.P.,Shahine, A.,Rossjohn, J. (登録日: 2021-05-19, 公開日: 2021-11-17, 最終更新日: 2024-11-13)

主引用文献

Reijneveld, J.F.,Marino, L.,Cao, T.P.,Cheng, T.Y.,Dam, D.,Shahine, A.,Witte, M.D.,Filippov, D.V.,Suliman, S.,van der Marel, G.A.,Moody, D.B.,Minnaard, A.J.,Rossjohn, J.,Codee, J.D.C.,Van Rhijn, I.
Rational design of a hydrolysis-resistant mycobacterial phosphoglycolipid antigen presented by CD1c to T cells.
J.Biol.Chem., 297:101197-101197, 2021

PubMed Abstract: Whereas proteolytic cleavage is crucial for peptide presentation by classical major histocompatibility complex (MHC) proteins to T cells, glycolipids presented by CD1 molecules are typically presented in an unmodified form. However, the mycobacterial lipid antigen mannosyl-β1-phosphomycoketide (MPM) may be processed through hydrolysis in antigen presenting cells, forming mannose and phosphomycoketide (PM). To further test the hypothesis that some lipid antigens are processed, and to generate antigens that lead to defined epitopes for future tuberculosis vaccines or diagnostic tests, we aimed to create hydrolysis-resistant MPM variants that retain their antigenicity. Here, we designed and tested three different, versatile synthetic strategies to chemically stabilize MPM analogs. Crystallographic studies of CD1c complexes with these three new MPM analogs showed anchoring of the lipid tail and phosphate group that is highly comparable to nature-identical MPM, with considerable conformational flexibility for the mannose head group. MPM-3, a difluoromethylene-modified version of MPM that is resistant to hydrolysis, showed altered recognition by cells, but not by CD1c proteins, supporting the cellular antigen processing hypothesis. Furthermore, the synthetic analogs elicited T cell responses that were cross-reactive with nature-identical MPM, fulfilling important requirements for future clinical use.

PubMed: 34536421
DOI: 10.1016/j.jbc.2021.101197

実験手法

X-RAY DIFFRACTION (2.11 Å)