Antibody Domain Exchange Is an Immunological Solution to Carbohydrate Cluster Recognition
Scripps Research Institute · University of Oxford
Abstract
Human antibody 2G12 neutralizes a broad range of human immunodeficiency virus type 1 (HIV-1) isolates by binding an unusually dense cluster of carbohydrate moieties on the "silent" face of the gp120 envelope glycoprotein. Crystal structures of Fab 2G12 and its complexes with the disaccharide Manalpha1-2Man and with the oligosaccharide Man9GlcNAc2 revealed that two Fabs assemble into an interlocked VH domain-swapped dimer. Further biochemical, biophysical, and mutagenesis data strongly support a Fab-dimerized antibody as the prevalent form that recognizes gp120. The extraordinary configuration of this antibody provides an extended surface, with newly described binding sites, for multivalent interaction with a…
Citation impact
- FWCI
- 15.35
- Percentile
- 100%
- References
- 56
Authors
16- DCD.A. Calarese
Scripps Research Institute, University of Oxford
- CNChristopher N. Scanlan
Scripps Research Institute, University of Oxford
- MBMichael B. Zwick
Scripps Research Institute, University of Oxford
- SDSongpon Deechongkit
Scripps Research Institute, University of Oxford
- YMYusuke Mimura
Scripps Research Institute, University of Oxford
Topics & keywords
- Epitope
- Glycoprotein
- Chemistry
- Antibody
- Disaccharide
- Oligosaccharide
- Immunoglobulin Fab Fragments
- Biochemistry
- Good health and well-being