Transient inactivation of hypothalamic hormone release to prevent post-traumatic stress sensitization

Informations projet

SECRET-DOCK

N° de convention de subvention: 101082277

DOI

10.3030/101082277

Projet clôturé

Date de signature de la CE 8 Juillet 2022

Date de début 1 Septembre 2022

Date de fin 29 Février 2024

Financé au titre de

• European Research Council (ERC)

Coût total

Aucune donnée

Contribution de l’UE

€ 150 000,00

Coordonné par

MEDIZINISCHE UNIVERSITAET WIEN
Austria

Periodic Reporting for period 1 - SECRET-DOCK (Transient inactivation of hypothalamic hormone release to prevent post-traumatic stress sensitization)

Période du rapport: 2022-09-01 au 2024-02-29

Résumé du contexte et des objectifs généraux du projet

Stress is the foremost consequence of human life, and became a pressing societal burden through the many sensory and societal pressures that have evolved during the past decades. Severe stress induces maladaptive changes in the brain that clinically manifest as post-traumatic stress disorder (PTSD). Despite ~4% of the population presenting PTSD, only symptomatic therapies are available. In the ’SECRET-CELLS’ ERC award, we have identified a multimodal neurocircuit that induces brain-wide sensitization to stress through the sequential recruitment of corticotropin releasing hormone (CRH)-containing neuroendocrine command cells in the hypothalamus and cortically-projecting norepinephrinergic neurons. Particularly, we developed mouse models to interrogate molecular underpinnings of fast, pulsatile hormone release from the hypothalamus into the blood stream. By using unbiased proteomics in combination with reverse single-cell transcriptomics to identify protein interactors, we have mapped probable druggable targets of an intracellular signaling cascade to inhibit the initiation and/or execution of hormone exocytosis. The 'SECRET-DOCK' project was aimed at evaluating the hypothesis that the inhibition of protein-protein interactions at hormone release sites could lead to the transient and reversible cessation of CRh release and peripheral sensitisation to stress.

Travail effectué depuis le début du projet jusqu’à la fin de la période considérée dans le rapport et principaux résultats atteints jusqu’à présent

We have first tested biochemical parameters (dynamics, stoichiometry) of direct protein-protein interactions by using recombinant proteins in vitro. Subsequently, we used X-ray crystallography to define the structure of druggable candidates in complex, with particular focus on their interaction sites/surfaces. Thereafter, a high-throughput screen was established to identify inhibitors. Templates were then used for small-molecule inhibitor discovery, in silico optimization, and the synthesis of derivatives. Finally, the candidates’ pharmacology and cytotoxicity were profiled in cells in vitro.

Progrès au-delà de l’état des connaissances et impact potentiel prévu (y compris l’impact socio-économique et les conséquences sociétales plus larges du projet jusqu’à présent)

We discovered novel protein-protein interactions that participate in the control of vesicle entry into and recycling within release terminals of hypothalamic neurons. Using a reverse template-inhibition screen, we have identified original compounds and their derivatives (179 in total), which significantly inhibited protein-protein interactions of biological relevance. Thereafter, we have synthesised 81 analogues of 4 lead compounds for structure-based optimisation. Finally, we have performed in-cell evaluation, including the assessment of general cytotoxicity and biological activity, on three cell lines (derived from human, rat and mouse, and with different cellular origins and characteristics), and scheduled hit-characterisation for the top 2 candidates. Thus, we have succeeded in 1) producing a novel biological theory, 2) defining the strucutural basis of this theory, 3) using the foreground knowledge to develop a screening platform, and 4) identifying, selecting, optimising, and testing for basic safety the lead compounds that could be amenable to reversibly inhibiting protein interactions, thus acutely reducing hormone release. Demonstration of biological activity, specificity for the site of action, and tolerability in model organisms will be necessary for IPR protection, investor identification, and commercialisation.

Residue conservation on the surface of secretagogin

Coexistence of target proteins in the endocrine pancreas