3PP4

Epitope characterization and crystal structure of GA101 provide insights into the molecular basis for the type I / type II distinction of anti- CD20 antibodies

3PP4 の概要

• エントリーDOI: 10.2210/pdb3pp4/pdb
• 関連するPDBエントリー: 3PP3
• 分子名称: GA101 Fab heavy chain, GA101 Fab light chain, B-lymphocyte antigen CD20, ... (5 entities in total)
• 機能のキーワード: antibody fab fragment ig-domain, cd20, cyclic peptide, antibody antigen, immune system
• 由来する生物種: Mus musculus (mouse); 詳細
• 細胞内の位置: Membrane; Multi-pass membrane protein: P11836
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 50822.21

構造登録者

Hopfner, K.-P.,Lammens, A. (登録日: 2010-11-24, 公開日: 2011-04-13, 最終更新日: 2024-10-30)

主引用文献

Niederfellner, G.,Lammens, A.,Mundigl, O.,Georges, G.J.,Schaefer, W.,Schwaiger, M.,Franke, A.,Wiechmann, K.,Jenewein, S.,Slootstra, J.W.,Timmerman, P.,Brannstrom, A.,Lindstrom, F.,Mossner, E.,Umana, P.,Hopfner, K.P.,Klein, C.
Epitope characterization and crystal structure of GA101 provide insights into the molecular basis for type I/II distinction of CD20 antibodies.
Blood, 118:358-367, 2011

PubMed Abstract: CD20 is a cell-surface marker of normal and malignant B cells. Rituximab, a monoclonal antibody targeting CD20, has improved the treatment of malignant lymphomas. Therapeutic CD20 antibodies are classified as either type I or II based on different mechanisms of killing malignant B cells. To reveal the molecular basis of this distinction, we fine-mapped the epitopes recognized by both types. We also determined the first X-ray structure of a type II antibody by crystallizing the obinutuzumab (GA101) Fab fragment alone and in complex with a CD20 cyclopeptide. Despite recognizing an overlapping epitope, GA101 binds CD20 in a completely different orientation than type I antibodies. Moreover, the elbow angle of GA101 is almost 30° wider than in type I antibodies, potentially resulting in different spatial arrangements of 2 CD20 molecules bound to a single GA101 or rituximab molecule. Using protein tomography, different CD20 complexes were found to be associated with the 2 antibodies, and confocal microscopy showed different membrane compartmentalization of these subpopulations of the cellular CD20 pool. Our findings offer a possible molecular explanation for the different cellular responses elicited by type I and II antibodies.

PubMed: 21444918
DOI: 10.1182/blood-2010-09-305847

実験手法

X-RAY DIFFRACTION (1.6 Å)