Identification of Broad-Spectrum MMP Inhibitors by Virtual Screening
Aleix Gimeno,
Doretta Cuffaro,
Elisa Nuti,
María José Ojeda-Montes,
Raúl Beltrán-Debón,
Miquel Mulero,
Armando Rossello,
Gerard Pujadas,
Santiago Garcia-Vallvé
Affiliations
Aleix Gimeno
Research Group in Cheminformatics & Nutrition, Departament de Bioquímica i Biotecnologia, Campus de Sescelades, Universitat Rovira i Virgili, 43007 Tarragona, Catalonia, Spain
Doretta Cuffaro
Department of Pharmacy, University of Pisa, Via Bonanno 6, 56126 Pisa, Italy
Elisa Nuti
Department of Pharmacy, University of Pisa, Via Bonanno 6, 56126 Pisa, Italy
María José Ojeda-Montes
Research Group in Cheminformatics & Nutrition, Departament de Bioquímica i Biotecnologia, Campus de Sescelades, Universitat Rovira i Virgili, 43007 Tarragona, Catalonia, Spain
Raúl Beltrán-Debón
Research Group in Cheminformatics & Nutrition, Departament de Bioquímica i Biotecnologia, Campus de Sescelades, Universitat Rovira i Virgili, 43007 Tarragona, Catalonia, Spain
Miquel Mulero
Research Group in Cheminformatics & Nutrition, Departament de Bioquímica i Biotecnologia, Campus de Sescelades, Universitat Rovira i Virgili, 43007 Tarragona, Catalonia, Spain
Armando Rossello
Department of Pharmacy, University of Pisa, Via Bonanno 6, 56126 Pisa, Italy
Gerard Pujadas
Research Group in Cheminformatics & Nutrition, Departament de Bioquímica i Biotecnologia, Campus de Sescelades, Universitat Rovira i Virgili, 43007 Tarragona, Catalonia, Spain
Santiago Garcia-Vallvé
Research Group in Cheminformatics & Nutrition, Departament de Bioquímica i Biotecnologia, Campus de Sescelades, Universitat Rovira i Virgili, 43007 Tarragona, Catalonia, Spain
Matrix metalloproteinases (MMPs) are the family of proteases that are mainly responsible for degrading extracellular matrix (ECM) components. In the skin, the overexpression of MMPs as a result of ultraviolet radiation triggers an imbalance in the ECM turnover in a process called photoaging, which ultimately results in skin wrinkling and premature skin ageing. Therefore, the inhibition of different enzymes of the MMP family at a topical level could have positive implications for photoaging. Considering that the MMP catalytic region is mostly conserved across different enzymes of the MMP family, in this study we aimed to design a virtual screening (VS) workflow to identify broad-spectrum MMP inhibitors that can be used to delay the development of photoaging. Our in silico approach was validated in vitro with 20 VS hits from the Specs library that were not only structurally different from one another but also from known MMP inhibitors. In this bioactivity assay, 18 of the 20 compounds inhibit at least one of the assayed MMPs at 100 μM (with 5 of them showing around 50% inhibition in all the tested MMPs at this concentration). Finally, this VS was used to identify natural products that have the potential to act as broad-spectrum MMP inhibitors and be used as a treatment for photoaging.