Tetra-anionic porphyrin mimics protein-protein interactions between regulatory particles and the catalytic core, allosterically activating human 20S proteasome

Decreased proteasome activity is a hallmark of brain and retinal neurodegenerative diseases (Alzheimer's, Parkinson's diseases, glaucoma) boosting the search for molecules acting as proteasome activators. Based on the hypothesis of an electrostatic key code driving catalytic core particle (20S) activation by regulatory particles (RPs), we identified the tetra-anionic meso-Tetrakis(4-sulphonatophenyl)-porphyrin (H2TPPS) as a new activator of human proteasome. By means of an integrated approach, including bioinformatics, enzymatic kinetic analysis, atomic force microscopy, and dynamic docking simulations, we show how binding of H2TPPS affects the closed/open conformational equilibrium of human 20S to ultimately promote substrate gate opening and proteolytic activity. These outcomes support our hypothesis and pave the way to the rational discovery of new proteasome allosteric modulators able to reproduce the key structural elements of regulatory particles responsible for catalytic activation.

Authors

Institutions

Publication Details

Journal
Journal of Enzyme Inhibition and Medicinal Chemistry
Published
2025-04-07
DOI
https://doi.org/10.1080/14756366.2025.2482892
Citations
2
Primary Topic
Ubiquitin and proteasome pathways
Type
article
Field-Weighted Citation Impact
1.61

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Tetra-anionic porphyrin mimics protein-protein interactions between regulatory particles and the catalytic core, allosterically activating human 20S proteasome

Alessandro D’Urso, Danilo Milardi, A. Cunsolo, Caterina Fattorusso et al.
2 citations
Journal of Enzyme Inhibition and Medicinal Chemistry
Ubiquitin and proteasome pathways
1.61
article

Tetra-anionic porphyrin mimics protein-protein interactions between regulatory particles and the catalytic core, allosterically activating human 20S proteasome

Alessandro D’Urso, Danilo Milardi, A. Cunsolo, Caterina Fattorusso, Marco Persico, Maria Gaczyńska, Roberto Purrello, Paweł A. Osmulski, О. В. Ткачук, Anna Maria Santoro, Massimo Coletta, Diego Sbardella, Grazia Raffaella Tundo
article en
2 citations

Abstract

Decreased proteasome activity is a hallmark of brain and retinal neurodegenerative diseases (Alzheimer's, Parkinson's diseases, glaucoma) boosting the search for molecules acting as proteasome activators. Based on the hypothesis of an electrostatic key code driving catalytic core particle (20S) activation by regulatory particles (RPs), we identified the tetra-anionic meso-Tetrakis(4-sulphonatophenyl)-porphyrin (H2TPPS) as a new activator of human proteasome. By means of an integrated approach, including bioinformatics, enzymatic kinetic analysis, atomic force microscopy, and dynamic docking simulations, we show how binding of H2TPPS affects the closed/open conformational equilibrium of human 20S to ultimately promote substrate gate opening and proteolytic activity. These outcomes support our hypothesis and pave the way to the rational discovery of new proteasome allosteric modulators able to reproduce the key structural elements of regulatory particles responsible for catalytic activation.

Journal of Enzyme Inhibition and Medicinal ChemistryVol. 40(1)
University of Rome Tor Vergata (IT), The University of Texas at San Antonio Health Science Center (US), National Academies of Sciences, Engineering, and Medicine (US), University of Catania (IT), Fondazione G.B. Bietti (IT), Epic Sciences (United States) (US), Institute of Crystallography (IT), The University of Texas at San Antonio (US), University of Naples Federico II (IT)
Ministero dell’Istruzione, dell’Università e della Ricerca
Openalex Percentile: Top 18%
Ubiquitin and proteasome pathways
1.61
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.