Hexameric Structure and Assembly of the Interleukin-6/IL-6 α-Receptor/gp130 Complex
Fairchild Semiconductor (United States) · Stanford University
Abstract
Interleukin-6 (IL-6) is an immunoregulatory cytokine that activates a cell-surface signaling assembly composed of IL-6, the IL-6 alpha-receptor (IL-6Ralpha), and the shared signaling receptor gp130. The 3.65 angstrom-resolution structure of the extracellular signaling complex reveals a hexameric, interlocking assembly mediated by a total of 10 symmetry-related, thermodynamically coupled interfaces. Assembly of the hexameric complex occurs sequentially: IL-6 is first engaged by IL-6Ralpha and then presented to gp130in the proper geometry to facilitate a cooperative transition into the high-affinity, signaling-competent hexamer. The quaternary structures of other IL-6/IL-12 family signaling complexes are likely…
Citation impact
- FWCI
- 11.67
- Percentile
- 100%
- References
- 22
Authors
4- MJMartin J. BoulangerCorresponding
Fairchild Semiconductor (United States), Stanford University
- DCDar‐Chone Chow
Fairchild Semiconductor (United States), Stanford University
- EEElena E. Brevnova
Fairchild Semiconductor (United States), Stanford University
- KCK. Christopher García
Fairchild Semiconductor (United States), Stanford University
Topics & keywords
- Glycoprotein 130
- Random hexamer
- Cell biology
- Receptor
- Signal transduction
- Extracellular
- Cytokine receptor
- Cytokine