A Synthetic Human Antibody Antagonizes IL-18Rβ Signaling Through an Allosteric Mechanism. Issue 4 (14th February 2020)
- Record Type:
- Journal Article
- Title:
- A Synthetic Human Antibody Antagonizes IL-18Rβ Signaling Through an Allosteric Mechanism. Issue 4 (14th February 2020)
- Main Title:
- A Synthetic Human Antibody Antagonizes IL-18Rβ Signaling Through an Allosteric Mechanism
- Authors:
- Liu, Shusu
Miersch, Shane
Li, Ping
Bai, Bingxin
Liu, Chunchun
Qin, Wenming
Su, Jie
Huang, Haiming
Pan, James
Sidhu, Sachdev S.
Wu, Donghui - Abstract:
- Abstract: The interleukin-18 subfamily belongs to the interleukin-1 family and plays an important role in modulating innate and adaptive immune responses. Dysregulation of IL-18 has been implicated in or correlated with numerous diseases, including inflammatory diseases, autoimmune disorders, and cancer. Thus, blockade of IL-18 signaling may offer therapeutic benefits in many pathological settings. Here, we report the development of synthetic human antibodies that target human IL-18Rβ and block IL-18-mediated IFN-γ secretion by inhibiting NF-κB and MAPK dependent pathways. The crystal structure of a potent antagonist antibody in complex with IL-18Rβ revealed inhibition through an unexpected allosteric mechanism. Our findings offer a novel means for therapeutic intervention in the IL-18 pathway and may provide a new strategy for targeting cytokine receptors. Graphical abstract: Binding of scFv 3131 to IL-18Rβ blocks formation of the IL-18/IL-18Rα/IL-18Rβ ternary complex. Superposition of IL-18Rβ in complex with scFv 3131 (PDB code: 6KN9 ) on to the ternary complex (PDB code: 3WO4 ) was performed using the D3 domains of the two IL-18Rβ molecules as reference. In the IL-18Rβ/scFv 3131 complex, IL-18Rβ is colored in magenta, and scFv 3131 is colored in dark grey (VH) and light grey (VL). In the IL-18/IL-18Rα/IL-18Rβ ternary complex, IL-18Rβ is colored in wheat, IL-18Rα is colored in cyan, and IL-18 is colored in yellow. The D1-D2 domains of IL-18Rβ undergo a 104° rotationAbstract: The interleukin-18 subfamily belongs to the interleukin-1 family and plays an important role in modulating innate and adaptive immune responses. Dysregulation of IL-18 has been implicated in or correlated with numerous diseases, including inflammatory diseases, autoimmune disorders, and cancer. Thus, blockade of IL-18 signaling may offer therapeutic benefits in many pathological settings. Here, we report the development of synthetic human antibodies that target human IL-18Rβ and block IL-18-mediated IFN-γ secretion by inhibiting NF-κB and MAPK dependent pathways. The crystal structure of a potent antagonist antibody in complex with IL-18Rβ revealed inhibition through an unexpected allosteric mechanism. Our findings offer a novel means for therapeutic intervention in the IL-18 pathway and may provide a new strategy for targeting cytokine receptors. Graphical abstract: Binding of scFv 3131 to IL-18Rβ blocks formation of the IL-18/IL-18Rα/IL-18Rβ ternary complex. Superposition of IL-18Rβ in complex with scFv 3131 (PDB code: 6KN9 ) on to the ternary complex (PDB code: 3WO4 ) was performed using the D3 domains of the two IL-18Rβ molecules as reference. In the IL-18Rβ/scFv 3131 complex, IL-18Rβ is colored in magenta, and scFv 3131 is colored in dark grey (VH) and light grey (VL). In the IL-18/IL-18Rα/IL-18Rβ ternary complex, IL-18Rβ is colored in wheat, IL-18Rα is colored in cyan, and IL-18 is colored in yellow. The D1-D2 domains of IL-18Rβ undergo a 104° rotation relative to the D3 domain in the two structures. Image 1 Highlights: IL-18/IL-18Rα/IL-18Rβ ternary complex is essential for downstream IFNγ secretion. Antibodies to human IL-18Rβ were identified from a phage-displayed antibody library. One antibody was identified as a potent antagonist to inhibit IFNγ secretion. Crystal structure shows the antibody can disturb the formation of the ternary complex. The antibody has the potential to treat diseases caused by excessive IL-18 activation. … (more)
- Is Part Of:
- Journal of molecular biology. Volume 432:Issue 4(2020)
- Journal:
- Journal of molecular biology
- Issue:
- Volume 432:Issue 4(2020)
- Issue Display:
- Volume 432, Issue 4 (2020)
- Year:
- 2020
- Volume:
- 432
- Issue:
- 4
- Issue Sort Value:
- 2020-0432-0004-0000
- Page Start:
- 1169
- Page End:
- 1182
- Publication Date:
- 2020-02-14
- Subjects:
- interleukin-1 family -- interleukin-18 subfamily -- IFN-γ -- antibody phage display -- crystal structure
Molecular biology -- Periodicals
Biology -- Periodicals
Biochemistry -- Periodicals
Bacteriology -- Periodicals
Molecular Biology -- Periodicals
Biochemistry -- Periodicals
Biologie moléculaire -- Périodiques
Biologie -- Périodiques
Biochimie -- Périodiques
Moleculaire biologie
Biochemistry
Biology
Molecular biology
Periodicals
572.805 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00222836 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jmb.2020.01.012 ↗
- Languages:
- English
- ISSNs:
- 0022-2836
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5020.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23138.xml