8QSA

Ternary structure of 14-3-3s, C-RAF phosphopeptide (pS259) and compound 86 (1084384)

Summary for 8QSA

• Entry DOI: 10.2210/pdb8qsa/pdb
• Descriptor: 14-3-3 protein sigma, C-RAF peptide, CHLORIDE ION, ... (6 entities in total)
• Functional Keywords: stabilizer, protein-protein interaction, peptide binding protein
• Biological source: Homo sapiens (human); More
• Total number of polymer chains: 2
• Total formula weight: 28299.18

Authors

Konstantinidou, M.,Vickery, H.,Pennings, M.A.M.,Virta, J.,Visser, E.J.,Oetelaar, M.C.M.,Overmans, M.,Neitz, J.,Ottmann, C.,Brunsveld, L.,Arkin, M.R. (deposition date: 2023-10-10, release date: 2025-04-23, Last modification date: 2026-03-04)

Primary citation

Konstantinidou, M.,Vickery, H.R.,Pennings, M.A.M.,Virta, J.M.,Luo, S.Y.,Visser, E.J.,Bannier, S.D.,Srikanth, M.,Cismoski, S.Z.,Young, L.C.,van den Oetelaar, M.C.M.,McCormick, F.,Ottmann, C.,Brunsveld, L.,Arkin, M.R.
Modulation of the 14-3-3 sigma /C-RAF "Auto"inhibited Complex by Molecular Glues.
J.Am.Chem.Soc., 148:4951-4965, 2026

PubMed Abstract: Molecular glues, compounds that bind cooperatively at protein-protein interfaces (PPIs), are revolutionizing chemical biology and drug discovery, allowing the modulation of traditional "undruggable" targets. Here, we focus on a native regulatory PPI between the scaffolding protein 14-3-3 and C-RAF, a key component of the MAPK signaling pathway. Extensive drug discovery efforts have focused on the MAPK pathway due to its central role in oncology and developmental disorders (RASopathies). However, the modulation of its protein complexes is underexplored. C-RAF activity is regulated on multiple levels including dimerization, phosphorylation, and complex formation with 14-3-3, which prevents C-RAF activation by binding to a C-RAF sequence centered on phospho-serine 259. We used a fragment-merging approach to design molecular glues that bound to the composite surface of this 14-3-3/C-RAFpS259 complex. Molecular glues stabilized the inhibitory complex up to 300-fold; their glue-based mechanism of action was confirmed by crystallography and biophysical studies. Selectivity among the other RAF isoforms and other RAF phosphorylation sites was evaluated. The best compounds showed excellent selectivity among a broad panel of 80 14-3-3 clients. Cellular assays demonstrated on-target engagement, enhanced phosphorylation levels of C-RAFpS259, and reduced levels of RAF dimerization and ERK phosphorylation. Overall, this approach enabled chemical biology studies for a C-RAF site that was intrinsically disordered prior to 14-3-3 binding and had not been targeted previously. These molecular glues will be useful chemical probes and starting points for drug discovery efforts to modulate native PPI stabilization in the MAPK pathway with applications in oncology and RASopathies.

PubMed: 41617210
DOI: 10.1021/jacs.5c12622

Experimental method

X-RAY DIFFRACTION (1.8 Å)