Structural basis for CD97 recognition of the decay-accelerating factor CD55 suggests mechanosensitive activation of adhesion GPCRs
| Autor: | Gaojie Song, Jie Yang, Shengzhao Xu, Na Li, Minghui Niu, Deqiang Yao, Jie Yan, Guisheng Zhong |
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| Rok vydání: | 2021 |
| Předmět: |
Models
Molecular 0301 basic medicine immune disorder Protein Conformation tensile force SPR surface plasmon resonance Crystallography X-Ray Biochemistry Receptors G-Protein-Coupled TEV tobacco etch virus 03 medical and health sciences Antigens CD Epidermal growth factor Humans structure Receptor Molecular Biology Decay-accelerating factor Binding selectivity shearing geometry G protein-coupled receptor EGF epidermal growth factor CD55 Antigens GAIN GPCR autoproteolysis-inducing 030102 biochemistry & molecular biology Chemistry SAXS small-angle X-ray scattering EGF module-containing mucin-like hormone receptor Cell Biology Adhesion adhesion GPCR Ligand (biochemistry) EMR EGF module–containing mucin-like hormone receptor HEK293 Cells 7TM seven-transmembrane 030104 developmental biology SCR short consensus repeat GPCRs G protein–coupled receptors Biophysics CD97 mechanosensing CD55 Protein Binding Research Article |
| Zdroj: | The Journal of Biological Chemistry |
| ISSN: | 0021-9258 |
| DOI: | 10.1016/j.jbc.2021.100776 |
| Popis: | The adhesion G protein–coupled receptor CD97 and its ligand complement decay-accelerating factor CD55 are important binding partners in the human immune system. Dysfunction in this binding has been linked to immune disorders such as multiple sclerosis and rheumatoid arthritis, as well as various cancers. Previous literatures have indicated that the CD97 includes 3 to 5 epidermal growth factor (EGF) domains at its N terminus and these EGF domains can bind to the N-terminal short consensus repeat (SCR) domains of CD55. However, the details of this interaction remain elusive, especially why the CD55 binds with the highest affinity to the shortest isoform of CD97 (EGF1,2,5). Herein, we designed a chimeric expression construct with the EGF1,2,5 domains of CD97 and the SCR1–4 domains of CD55 connected by a flexible linker and determined the complex structure by crystallography. Our data reveal that the two proteins adopt an overall antiparallel binding mode involving the SCR1–3 domains of CD55 and all three EGF domains of CD97. Mutagenesis data confirmed the importance of EGF5 in the interaction and explained the binding specificity between CD55 and CD97. The architecture of CD55–CD97 binding mode together with kinetics suggests a force-resisting shearing stretch geometry when forces applied to the C termini of both proteins in the circulating environment. The potential of the CD55–CD97 complex to withstand tensile force may provide a basis for the mechanosensing mechanism for activation of adhesion G protein–coupled receptors. |
| Databáze: | OpenAIRE |
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