8CDG

Crystal structure of human IL-17A cytokine in complex with macrocycle

8CDG の概要

• エントリーDOI: 10.2210/pdb8cdg/pdb
• 分子名称: Interleukin-17A, (9~{S},12~{R},19~{S})-9-[[4-[[(2~{S})-2-cyclohexyl-2-(2-phenylethanoylamino)ethanoyl]amino]phenyl]methyl]-12-methyl-7,10,13,21-tetrakis(oxidanylidene)-8,11,14,20-tetrazaspiro[4.17]docosane-19-carboxylic acid (2 entities in total)
• 機能のキーワード: inhibitor, complex, cytokine, macrocycle
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 29405.15

構造登録者

Schulze, M.-S. (登録日: 2023-01-30, 公開日: 2023-12-06, 最終更新日: 2024-10-16)

主引用文献

Shaw, D.J.,Waters, L.C.,Strong, S.L.,Schulze, M.E.D.,Greetham, G.M.,Towrie, M.,Parker, A.W.,Prosser, C.E.,Henry, A.J.,Lawson, A.D.G.,Carr, M.D.,Taylor, R.J.,Hunt, N.T.,Muskett, F.W.
Modulation of IL-17 backbone dynamics reduces receptor affinity and reveals a new inhibitory mechanism.
Chem Sci, 14:7524-7536, 2023

PubMed Abstract: Knowledge of protein dynamics is fundamental to the understanding of biological processes, with NMR and 2D-IR spectroscopy being two of the principal methods for studying protein dynamics. Here, we combine these two methods to gain a new understanding of the complex mechanism of a cytokine:receptor interaction. The dynamic nature of many cytokines is now being recognised as a key property in the signalling mechanism. Interleukin-17s (IL-17) are proinflammatory cytokines which, if unregulated, are associated with serious autoimmune diseases such as psoriasis, and although there are several therapeutics on the market for these conditions, small molecule therapeutics remain elusive. Previous studies, exploiting crystallographic methods alone, have been unable to explain the dramatic differences in affinity observed between IL-17 dimers and their receptors, suggesting there are factors that cannot be fully explained by the analysis of static structures alone. Here, we show that the IL-17 family of cytokines have varying degrees of flexibility which directly correlates to their receptor affinities. Small molecule inhibitors of the cytokine:receptor interaction are usually thought to function by either causing steric clashes or structural changes. However, our results, supported by other biophysical methods, provide evidence for an alternate mechanism of inhibition, in which the small molecule rigidifies the protein, causing a reduction in receptor affinity. The results presented here indicate an induced fit model of cytokine:receptor binding, with the more flexible cytokines having a higher affinity. Our approach could be applied to other systems where the inhibition of a protein-protein interaction has proved intractable, for example due to the flat, featureless nature of the interface. Targeting allosteric sites which modulate protein dynamics, opens up new avenues for novel therapeutic development.

PubMed: 37449080
DOI: 10.1039/d3sc00728f

実験手法

X-RAY DIFFRACTION (2.9 Å)