Polypharmacological Perturbation of the 14-3-3 Adaptor Protein Interactome Stimulates Neurite Outgrowth. Issue 6 (18th June 2020)
- Record Type:
- Journal Article
- Title:
- Polypharmacological Perturbation of the 14-3-3 Adaptor Protein Interactome Stimulates Neurite Outgrowth. Issue 6 (18th June 2020)
- Main Title:
- Polypharmacological Perturbation of the 14-3-3 Adaptor Protein Interactome Stimulates Neurite Outgrowth
- Authors:
- Kaplan, Andrew
Andrei, Sebastian A.
van Regteren Altena, Anna
Simas, Tristan
Banerjee, Sara L.
Kato, Nobuo
Bisson, Nicolas
Higuchi, Yusuke
Ottmann, Christian
Fournier, Alyson E. - Abstract:
- Summary: Targeting protein-protein interactions (PPIs) is a promising approach in the development of drugs for many indications. 14-3-3 proteins are a family of phosphoprotein-binding molecules with critical functions in dozens of cell signaling networks. 14-3-3s are abundant in the central nervous system, and the small molecule fusicoccin-A (FC-A), a tool compound that can be used to manipulate 14-3-3 PPIs, enhances neurite outgrowth in cultured neurons. New semisynthetic FC-A derivatives with improved binding affinity for 14-3-3 complexes have recently been developed. Here, we use a series of screens that identify these compounds as potent inducers of neurite outgrowth through a polypharmacological mechanism. Using proteomics and X-ray crystallography, we discover that these compounds extensively regulate the 14-3-3 interactome by stabilizing specific PPIs, while disrupting others. These results provide new insights into the development of drugs to target 14-3-3 PPIs, a potential therapeutic strategy for CNS diseases. Graphical Abstract: Highlights: FC-A is a small molecule that modulates 14-3-3 PPIs and induces neurite outgrowth Derivatives with improved potency were identified in a neurite outgrowth screen Interactome analysis reveals regulation of 14-3-3 PPIs enriched in Rap1 network Derivative FC-NCPC can stabilize or competitively inhibit 14-3-3 PPIs Abstract : Kaplan et al. identify a derivative of the small molecule fusicoccin-A (FC-A) that stimulates neuriteSummary: Targeting protein-protein interactions (PPIs) is a promising approach in the development of drugs for many indications. 14-3-3 proteins are a family of phosphoprotein-binding molecules with critical functions in dozens of cell signaling networks. 14-3-3s are abundant in the central nervous system, and the small molecule fusicoccin-A (FC-A), a tool compound that can be used to manipulate 14-3-3 PPIs, enhances neurite outgrowth in cultured neurons. New semisynthetic FC-A derivatives with improved binding affinity for 14-3-3 complexes have recently been developed. Here, we use a series of screens that identify these compounds as potent inducers of neurite outgrowth through a polypharmacological mechanism. Using proteomics and X-ray crystallography, we discover that these compounds extensively regulate the 14-3-3 interactome by stabilizing specific PPIs, while disrupting others. These results provide new insights into the development of drugs to target 14-3-3 PPIs, a potential therapeutic strategy for CNS diseases. Graphical Abstract: Highlights: FC-A is a small molecule that modulates 14-3-3 PPIs and induces neurite outgrowth Derivatives with improved potency were identified in a neurite outgrowth screen Interactome analysis reveals regulation of 14-3-3 PPIs enriched in Rap1 network Derivative FC-NCPC can stabilize or competitively inhibit 14-3-3 PPIs Abstract : Kaplan et al. identify a derivative of the small molecule fusicoccin-A (FC-A) that stimulates neurite outgrowth by regulating dozens of protein-protein interactions (PPIs) in the 14-3-3 adaptor protein interactome. This compound, FC-NCPC, bidirectionally stabilizes and inhibits 14-3-3 PPIs enriched within the Rap1 signaling network, suggesting new targets for CNS indications. … (more)
- Is Part Of:
- Cell chemical biology. Volume 27:Issue 6(2020)
- Journal:
- Cell chemical biology
- Issue:
- Volume 27:Issue 6(2020)
- Issue Display:
- Volume 27, Issue 6 (2020)
- Year:
- 2020
- Volume:
- 27
- Issue:
- 6
- Issue Sort Value:
- 2020-0027-0006-0000
- Page Start:
- 657
- Page End:
- 667.e6
- Publication Date:
- 2020-06-18
- Subjects:
- polypharmacology -- axon -- 14-3-3 -- regeneration -- Rap1 -- spinal cord injury
Biochemistry -- Periodicals
572.05 - Journal URLs:
- http://www.cell.com/cell-chemical-biology/home ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.chembiol.2020.02.010 ↗
- Languages:
- English
- ISSNs:
- 2451-9456
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3097.733000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13353.xml