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4ACP

Deactivation of human IgG1 Fc by endoglycosidase treatment

4ACP の概要
エントリーDOI10.2210/pdb4acp/pdb
関連するPDBエントリー1AJ7 1AQK 1BEY 1D5B 1D5I 1D6V 1DN2 1E4K 1FC1 1FC2 1FCC 1H3T 1H3U 1H3V 1H3W 1H3Y 1I7Z 1L6X 1OQX 1T83 1T89 2IWG 2J6E 2RCS 2WAH
分子名称IG GAMMA-1 CHAIN C REGION, 2-acetamido-2-deoxy-beta-D-glucopyranose (3 entities in total)
機能のキーワードimmune system, igg, antibody, kifunensine
由来する生物種HOMO SAPIENS (HUMAN)
細胞内の位置Secreted: P01857
タンパク質・核酸の鎖数2
化学式量合計54252.26
構造登録者
Raman, K.,Bowden, T.A.,Krishna, B.A.,Dwek, R.A.,Crispin, M.,Scanlan, C.N. (登録日: 2011-12-16, 公開日: 2012-04-25, 最終更新日: 2023-12-20)
主引用文献Baruah, K.,Bowden, T.A.,Krishna, B.A.,A Dwek, R.,Crispin, M.,Scanlan, C.N.
Selective Deactivation of Serum Igg: A General Strategy for the Enhancement of Monoclonal Antibody Receptor Interactions.
J.Mol.Biol., 420:1-, 2012
Cited by
PubMed Abstract: Serum IgG is a potent inhibitor of monoclonal antibody (mAb) binding to the cell-surface Fcγ receptors (FcγRs), which mediate cytotoxic and phagocytic effector functions. Here, we show that this competition can be eliminated, selectively, by the introduction to serum of (i) an enzyme that displaces Fc from FcγRs and (ii) a modification present in the therapeutic mAb that renders it resistant to that enzyme. Specifically, we show that (i) EndoS (endoglycosidase S) cleaves only complex-type glycans of the type found on IgG but (ii) is inactive against an engineered IgG Fc with oligomannose-type glycans. EndoS thus reduces FcγR binding of serum IgG, but not that of engineered mAb. Introduction of both the engineered mAb and endoglycosidase in serum leads to a dramatic increase in FcγR binding compared to the introduction of mAb in serum alone. Antibody receptor refocusing is a general technique for boosting the effector signal of therapeutic antibodies.
PubMed: 22484364
DOI: 10.1016/J.JMB.2012.04.002
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.49 Å)
構造検証レポート
Validation report summary of 4acp
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-10-30に公開中

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