3QFD

Human Class I MHC HLA-A2 in complex with Mart-1(27-35) nonameric peptide

3QFD の概要

• エントリーDOI: 10.2210/pdb3qfd/pdb
• 関連するPDBエントリー: 2GUO
• 分子名称: HLA class I histocompatibility antigen, A-2 alpha chain, Beta-2-microglobulin, Mart-1(27-35) peptide, ... (6 entities in total)
• 機能のキーワード: mart-1 peptide, nonapeptide, mhc class i, hla-a2, tcr a6, cross-reactivity, melanoma, immune system
• 由来する生物種: Homo sapiens (human); 詳細
• 細胞内の位置: Membrane; Single-pass type I membrane protein: P01892; Secreted: P61769
• タンパク質・核酸の鎖数: 6
• 化学式量合計: 89693.63

構造登録者

Borbulevych, O.Y.,Baker, B.M. (登録日: 2011-01-21, 公開日: 2011-09-28, 最終更新日: 2024-11-27)

主引用文献

Insaidoo, F.K.,Borbulevych, O.Y.,Hossain, M.,Santhanagopolan, S.M.,Baxter, T.K.,Baker, B.M.
Loss of T Cell Antigen Recognition Arising from Changes in Peptide and Major Histocompatibility Complex Protein Flexibility: IMPLICATIONS FOR VACCINE DESIGN.
J.Biol.Chem., 286:40163-40173, 2011

PubMed Abstract: Modification of the primary anchor positions of antigenic peptides to improve binding to major histocompatibility complex (MHC) proteins is a commonly used strategy for engineering peptide-based vaccine candidates. However, such peptide modifications do not always improve antigenicity, complicating efforts to design effective vaccines for cancer and infectious disease. Here we investigated the MART-1(27-35) tumor antigen, for which anchor modification (replacement of the position two alanine with leucine) dramatically reduces or ablates antigenicity with a wide range of T cell clones despite significantly improving peptide binding to MHC. We found that anchor modification in the MART-1(27-35) antigen enhances the flexibility of both the peptide and the HLA-A*0201 molecule. Although the resulting entropic effects contribute to the improved binding of the peptide to MHC, they also negatively impact T cell receptor binding to the peptide·MHC complex. These results help explain how the "anchor-fixing" strategy fails to improve antigenicity in this case, and more generally, may be relevant for understanding the high specificity characteristic of the T cell repertoire. In addition to impacting vaccine design, modulation of peptide and MHC flexibility through changes to antigenic peptides may present an evolutionary strategy for the escape of pathogens from immune destruction.

PubMed: 21937447
DOI: 10.1074/jbc.M111.283564

実験手法

X-RAY DIFFRACTION (1.68 Å)