Cited by 254Monoclonal and Polyclonal Antibodies ResearchT-cell and B-cell ImmunologyProtein Structure and Dynamics

Flexibility of human IgG subclasses

Roux, K H, Strelets, L, Michaelsen, T E·1997·The Journal of Immunology

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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Crossref · 10.4049/jimmunol.159.7.3372

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Cited by 254

Authors
Roux, K. H., Strelets, L., & Michaelsen, T. E.
Affiliations
Florida State University (US)
Venue
The Journal of Immunology
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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