NatureBiochemistryPeer-reviewed journal article
Design of facilitated dissociation enables control over cytokine signaling duration
Adam J. BroermaniD, Christoph PollmanniD, Yang ZhaoiD, Mauriz A. LichtensteiniD, Mark D. Jackson, Maxx H. TessmeriD, Won Hee RyuiD, Masato OgishiiD, Mohamad H. AbediiD, Danny D. SahtoeiD, Aza AlleniD, Alex KangiD, Joshmyn De La CruziD, Evans BrackenbroughiD, Banumathi SankaraniD, Asim K. BeraiD, Daniel M. ZuckermaniD, Stefan StolliD, K. Christopher GarcíaiD, Florian PraetoriusiD, Jacob PiehleriD, David A. BakeriD
Abstract
Protein design has focused primarily on the design of ground states, ensuring they are sufficiently low energy to be highly populated1. Designing the kinetics and dynamics of a system requires, in addition, the design of excited states that are traversed in transitions from one low-lying state to another2,3. This is a challenging task as such states must be sufficiently strained to be poorly populated, but not so strained that they are not populated at all, and because protein design methods have generally focused on creating near-ideal structures4-7. Here we describe a general approach for designing systems which use an induced-fit power stroke8 to generate a structurally frustrated9 and strained excited state, allosterically driving protein complex dissociation. X-ray crystallography, double electron-electron resonance spectroscopy, and kinetic binding measurements demonstrate that incorporating excited states enables design of effector-induced increases in dissociation rates as high as 6000-fold. We highlight the power of this approach by designing cytokine mimics which can be dissociated within seconds from their receptors.
- Citations
- 29
- FWCI
- 8.01
- Field percentile
- top 1%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Protein-ligand binding kinetics are primarily controlled by the protein, not the ligand.
Bharath Srinivasan, Ana Corrionero, … Peter J. Tonge·bioRxiv·May 22, 2026
- Analysis of the dynamics of a complex, multipathway reaction: Insulin dimer dissociation
Kwanghoon Jeong, Spencer C. Guo, … Aaron R. Dinner·The Journal of Physical Chemistry BPeer-reviewed·Dec 13, 2024
- Force-dependent facilitated dissociation can generate protein-DNA catch bonds
K. Dahlke, J. Zhao, … E. J. Banigan·bioRxiv·Jul 9, 2019
- De novo design of allosterically switchable protein assemblies
- Rational design of proteins that exchange on functional timescales
J. A. Davey, A. M. Damry, … R. A. Chica·bioRxiv·Mar 3, 2017
- Dissection of ligand-CDK8/CycC unbinding free energy barriers and kinetics by molecular simulations
Z. Tang, S.-H. Chen, C.-e. A. Chang·bioRxiv·Jun 22, 2019