4ODS
Unliganded Fab structure of lipid A-specific antibody S55-3
4ODS の概要
| エントリーDOI | 10.2210/pdb4ods/pdb |
| 関連するPDBエントリー | 4ODT 4ODU 4ODV 4ODW 4ODY 4ODZ 4OE0 |
| 分子名称 | S55-3 Fab (IgG2b) heavy chain (3 entities in total) |
| 機能のキーワード | carbohydrate binding, immune system |
| 由来する生物種 | Mus musculus 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 47487.60 |
| 構造登録者 | |
| 主引用文献 | Haji-Ghassemi, O.,Muller-Loennies, S.,Rodriguez, T.,Brade, L.,Kosma, P.,Brade, H.,Evans, S.V. Structural Basis for Antibody Recognition of Lipid A: INSIGHTS TO POLYSPECIFICITY TOWARD SINGLE-STRANDED DNA. J.Biol.Chem., 290:19629-19640, 2015 Cited by PubMed Abstract: Septic shock is a leading cause of death, and it results from an inflammatory cascade triggered by the presence of microbial products in the blood. Certain LPS from Gram-negative bacteria are very potent inducers and are responsible for a high percentage of septic shock cases. Despite decades of research, mAbs specific for lipid A (the endotoxic principle of LPS) have not been successfully developed into a clinical treatment for sepsis. To understand the molecular basis for the observed inability to translate in vitro specificity for lipid A into clinical potential, the structures of antigen-binding fragments of mAbs S1-15 and A6 have been determined both in complex with lipid A carbohydrate backbone and in the unliganded form. The two antibodies have separate germ line origins that generate two markedly different combining-site pockets that are complementary both in shape and charge to the antigen. mAb A6 binds lipid A through both variable light and heavy chain residues, whereas S1-15 utilizes exclusively the variable heavy chain. Both antibodies bind lipid A such that the GlcN-O6 attachment point for the core oligosaccharide is buried in the combining site, which explains the lack of LPS recognition. Longstanding reports of polyspecificity of anti-lipid A antibodies toward single-stranded DNA combined with observed homology of S1-15 and A6 and the reports of several single-stranded DNA-specific mAbs prompted the determination of the structure of S1-15 in complex with single-stranded DNA fragments, which may provide clues about the genesis of autoimmune diseases such as systemic lupus erythematosus, thyroiditis, and rheumatic autoimmune diseases. PubMed: 26085093DOI: 10.1074/jbc.M115.657874 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.94 Å) |
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