Literature DB >> 7888072

The structural requirements for complement activation by IgG: does it hinge on the hinge?

O H Brekke1, T E Michaelsen, I Sandlie.   

Abstract

The flexibility of antibody molecules principally derives from the structure of the hinge region. It has generally been accepted that the flexibility of the IgG hinge is necessary for complement activation to occur; however, recent studies dispute this premise. As described here by Ole Henrik Brekke, Terje Michaelsen and Inger Sandlie, it now appears that the only requirement of the hinge region for complement activation is the presence of inter-heavy-chain disulfide bond(s). Furthermore, the structural basis for the differences between IgG subclasses with respect to effector functions appear to be located within the CH2 domain of the immunoglobulin molecule.

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Year:  1995        PMID: 7888072     DOI: 10.1016/0167-5699(95)80094-8

Source DB:  PubMed          Journal:  Immunol Today        ISSN: 0167-5699


  27 in total

1.  Elbow flexibility and ligand-induced domain rearrangements in antibody Fab NC6.8: large effects of a small hapten.

Authors:  C A Sotriffer; B M Rode; J M Varga; K R Liedl
Journal:  Biophys J       Date:  2000-08       Impact factor: 4.033

2.  Complement component C1q enhances the biological activity of influenza virus hemagglutinin-specific antibodies depending on their fine antigen specificity and heavy-chain isotype.

Authors:  Jing Qi Feng; Krystyna Mozdzanowska; Walter Gerhard
Journal:  J Virol       Date:  2002-02       Impact factor: 5.103

3.  Identification of IgF, a hinge-region-containing Ig class, and IgD in Xenopus tropicalis.

Authors:  Yaofeng Zhao; Qiang Pan-Hammarström; Shuyang Yu; Nancy Wertz; Xiaofeng Zhang; Ning Li; John E Butler; Lennart Hammarström
Journal:  Proc Natl Acad Sci U S A       Date:  2006-07-28       Impact factor: 11.205

Review 4.  Fragmentation of monoclonal antibodies.

Authors:  Josef Vlasak; Roxana Ionescu
Journal:  MAbs       Date:  2011-05-01       Impact factor: 5.857

5.  The solution structures of two human IgG1 antibodies show conformational stability and accommodate their C1q and FcγR ligands.

Authors:  Lucy E Rayner; Gar Kay Hui; Jayesh Gor; Richard K Heenan; Paul A Dalby; Stephen J Perkins
Journal:  J Biol Chem       Date:  2015-02-06       Impact factor: 5.157

6.  ImmunoPET of Malignant and Normal B Cells with 89Zr- and 124I-Labeled Obinutuzumab Antibody Fragments Reveals Differential CD20 Internalization In Vivo.

Authors:  Kirstin A Zettlitz; Richard Tavaré; Scott M Knowles; Kristopher K Steward; John M Timmerman; Anna M Wu
Journal:  Clin Cancer Res       Date:  2017-09-19       Impact factor: 12.531

7.  Histidine residue mediates radical-induced hinge cleavage of human IgG1.

Authors:  Zac Yates; Kannan Gunasekaran; Hongxing Zhou; Zhonghua Hu; Zhi Liu; Randal R Ketchem; Boxu Yan
Journal:  J Biol Chem       Date:  2010-03-19       Impact factor: 5.157

8.  Expanding the Scope of Antibody Rebridging with New Pyridazinedione-TCO Constructs.

Authors:  Angela N Marquard; Jonathan C T Carlson; Ralph Weissleder
Journal:  Bioconjug Chem       Date:  2020-04-28       Impact factor: 4.774

9.  Complementary MS methods assist conformational characterization of antibodies with altered S-S bonding networks.

Authors:  Lisa M Jones; Hao Zhang; Weidong Cui; Sandeep Kumar; Justin B Sperry; James A Carroll; Michael L Gross
Journal:  J Am Soc Mass Spectrom       Date:  2013-03-13       Impact factor: 3.109

10.  Human IgG2 antibodies display disulfide-mediated structural isoforms.

Authors:  Jette Wypych; Ming Li; Amy Guo; Zhongqi Zhang; Theresa Martinez; Martin J Allen; Szilan Fodor; Drew N Kelner; Gregory C Flynn; Yaoqing Diana Liu; Pavel V Bondarenko; Margaret Speed Ricci; Thomas M Dillon; Alain Balland
Journal:  J Biol Chem       Date:  2008-03-13       Impact factor: 5.157

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