6MOG

Dimeric DARPin C_R3

6MOG の概要

• エントリーDOI: 10.2210/pdb6mog/pdb
• 分子名称: DARPin C_R3, 1,2-ETHANEDIOL, TRIETHYLENE GLYCOL, ... (4 entities in total)
• 機能のキーワード: darpin, biosynthetic protein
• 由来する生物種: synthetic construct
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 35901.07

構造登録者

Jude, K.M.,Mohan, K.,Garcia, K.C. (登録日: 2018-10-04, 公開日: 2019-06-05, 最終更新日: 2024-04-03)

主引用文献

Mohan, K.,Ueda, G.,Kim, A.R.,Jude, K.M.,Fallas, J.A.,Guo, Y.,Hafer, M.,Miao, Y.,Saxton, R.A.,Piehler, J.,Sankaran, V.G.,Baker, D.,Garcia, K.C.
Topological control of cytokine receptor signaling induces differential effects in hematopoiesis.
Science, 364:-, 2019

PubMed Abstract: Although tunable signaling by G protein-coupled receptors can be exploited through medicinal chemistry, a comparable pharmacological approach has been lacking for the modulation of signaling through dimeric receptors, such as those for cytokines. We present a strategy to modulate cytokine receptor signaling output by use of a series of designed C2-symmetric cytokine mimetics, based on the designed ankyrin repeat protein (DARPin) scaffold, that can systematically control erythropoietin receptor (EpoR) dimerization orientation and distance between monomers. We sampled a range of EpoR geometries by varying intermonomer angle and distance, corroborated by several ligand-EpoR complex crystal structures. Across the range, we observed full, partial, and biased agonism as well as stage-selective effects on hematopoiesis. This surrogate ligand strategy opens access to pharmacological modulation of therapeutically important cytokine and growth factor receptor systems.

PubMed: 31123111
DOI: 10.1126/science.aav7532

実験手法

X-RAY DIFFRACTION (1.21 Å)