Evidence map›Paper›PMID 40417780›Full record

ArticleJournal of neurochemistry2025

A Computational Approach to Identify Novel Protein Targets Uncovers New Potential Mechanisms of Action of Mirtazapine S(+) and R(-) Enantiomers in Rett Syndrome.

Ottavia Maria Roggero, Nicolò Gualandi, Viviana Ciraci, Vittoria Berutto, Emanuele Carosati, Enrico Tongiorgi

Abstract read
In one paragraph

Article in Journal of neurochemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Antibiotics (Basel, Switzerland) · 2026
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Ottavia Maria RoggeroCellular and Developmental Neurobiology Lab-Department of Life Sciences, University of Trieste, Trieste, Italy.ORCID 0000-0002-7159-5262
Nicolò GualandiComputational Genomics Laboratory, Scuola Internazionale Superiore di Studi Avanzati (SISSA), Trieste, Italy.ORCID 0000-0003-0622-6118
Viviana CiraciCellular and Developmental Neurobiology Lab-Department of Life Sciences, University of Trieste, Trieste, Italy.ORCID 0000-0003-1812-3204
Vittoria BeruttoCellular and Developmental Neurobiology Lab-Department of Life Sciences, University of Trieste, Trieste, Italy.ORCID 0009-0003-6764-8450
Emanuele CarosatiDepartment of Chemical and Pharmaceutical Sciences, University of Trieste, Trieste, Italy.ORCID 0000-0003-0657-5035
Enrico TongiorgiCellular and Developmental Neurobiology Lab-Department of Life Sciences, University of Trieste, Trieste, Italy.ORCID 0000-0003-0485-0603

Funding

Fondation Jérôme LejeuneMinistero dell'Università e della Ricerca PRIN - BRAIN n. Prot 2022KL2ECAPro Rett ricerca ONLUS
6 · The paper itself

Abstract

Rett syndrome (RTT) is a progressive neurodevelopmental disorder that affects approximately 1:10000 newborn girls and is primarily caused by mutations in the X-linked gene MECP2. Due to reduced brain monoamine levels in RTT, antidepressants have been explored as potential therapies. In previous studies, we demonstrated that the antidepressant mirtazapine (MTZ) alleviates symptoms in Mecp2-mutant mice and RTT adult patients. However, the mechanism of action of MTZ, a racemic mixture that binds to multiple receptors, remains unclear. This study introduces a computational approach to screen the "human pocketome," comprising over 25 K ligand-bound pockets derived from more than 210 K human protein structures available in the RCSB Protein Data Bank, aiming to identify binding pockets with high affinity for each MTZ enantiomer. Novelty concerns the approach to compare the two enantiomers of MTZ to other drugs experimentally determined as inactive for RTT. This approach introduces a new metric, the ZZscore, which ranks tested proteins and pockets based on their degree of interaction with the tested drugs. This enables the identification of potential drug-protein interactions relevant to the disease and/or phenotypic traits under study. Initial relaxed settings and thresholds parameters suggested over 30 potential targets, among which the RASH/SOS1 complex, but in vitro experiments on cultured hippocampal neurons from Mecp2-KO mice excluded any MTZ effect on it. Thus, we refined the procedure with more stringent parameters and identified 16 protein targets for S(+)MTZ and 14 for R(-)MTZ, with 5 common targets. Pathway enrichment analysis revealed 25 pathways for S(+)MTZ and 24 for R(-)MTZ, with 11 common pathways, many related to MeCP2 functions disrupted in RTT, such as epigenetic chromatin regulation, intracellular signaling, energy metabolism, cholesterol and lipid metabolism, and catecholamine biosynthesis. Overall, the presented computational modeling strategy for target identification allowed us to hypothesize new mechanisms of action for the two MTZ enantiomers.

Indexed as

MirtazapineRett SyndromeAnimalsFemaleHumansMethyl-CpG-Binding Protein 2MiceMolecular Docking SimulationStereoisomerismMethyl-CpG-Binding Protein 2MirtazapineantidepressantsBioGPSdrug‐protein dockingintellectual disabilitymirtazapineRett syndrometarget deconvolution

Identifiers

PMID40417780
PMCPMC12104967

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.