Flexibility of human IgG subclasses
Abstract
A variable region (Id)-matched set of genetically engineered human IgG1, -2, -3, and -4 subclass molecules was analyzed by electron microscopy for hinge-mediated differences in flexibility. The hinge-mediated bending was studied, as was the ability of the subclasses to form immune complexes with two anti-Id mAbs. The data show that the rank order (most to least flexible) of the IgG subclasses for hinge-folding mode of flexibility between Fab arms is IgG3 > IgG1 > IgG4 > IgG2. The mean Fab-Fab angles for the subclasses are IgG3, 136 degrees; IgG4, 128 degrees; IgG2, 127 degrees; and IgG1, 117 degrees. Fab-Fc angles were similarly analyzed. By sampling of equimolar mixtures of Id-bearing IgGs and each of two anti-Id mAb after incubation over time (1.5 min to 3.5 h), different kinetic profiles of immune complex formation of defined geometry were documented. Both anti-Id mAbs displayed unique kinetic profiles when complexed with the four IgG subclass molecules but also shared important features. Most notable was the higher propensity to form closed bivalent ring Id-anti-Id dimers with IgG3 than with IgG2 and IgG4. IgG1 was intermediate in its ability to form such dimers.
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IgG2 has a uniquely short hinge region, comprising 12 amino acids and containing a poly-proline double helix stabilized by four inter-heavy chain disulfide bridges.
“IgG2 has been demonstrated to have a uniquely short hinge region, comprising 12 amino acids and containing a poly-proline double helix, stabilized by four inter-heavy chain disulfide bridges (72).”
From Factors Affecting the FcRn-Mediated Transplacental Transfer of Antibodies and Implications for Vaccination in Pregnancy (2017) · cites this paper as [72]
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Cited by 254
- Authors
- Roux, K. H., Strelets, L., & Michaelsen, T. E.
- Affiliations
- Florida State University (US)
- ORCID
- Michaelsen, T E
- Venue
- The Journal of Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 1997-10-01
- Volume
- 159
- Issue
- 7
- Pages
- 3372-3382
- ISSN
- 0022-1767 (ISSN-L)
- 1550-6606
- OpenAlex
- W2108791168
- Cited by
- 254
- References
- 0
- Citations by year
- 2026: 11 · 2025: 12 · 2024: 11 · 2023: 16 · 2022: 13 · 2021: 13 · 2020: 11 · 2019: 13 · 2018: 8 · 2017: 6 · 2016: 13 · 2015: 9 · 2014: 12 · 2013: 10 · 2012: 8
- FWCI
- 6.81
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Immunology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Keywords
- hinge flexibility, hinge bending, immune complex formation, anti-idiotypic antibodies, IgG3, IgG1, IgG2, IgG4
- MeSH terms
- Animals, Antibodies, Anti-Idiotypic, Antibodies, Monoclonal, Antigen-Antibody Complex, Cell Line, Humans, Immunoglobulin G, Immunoglobulin Idiotypes, Immunoglobulin Variable Region, Immunoglobulin Fab Fragments, Immunoglobulin Heavy Chains, Immunoglobulin Light Chains, Structure-Activity Relationship, Protein Folding, Mice
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