Articles producció científica> Bioquímica i Biotecnologia

Understanding the variability of the S1' pocket to improve matrix metalloproteinase inhibitor selectivity profiles

  • Dades identificatives

    Identificador:  imarina:5873566
    Autors:  Gimeno, Aleix; Beltran-Debon, Raul; Mulero, Miguel; Pujadas, Gerard; Garcia-Vallve, Santiago
    Resum:
    Matrix metalloproteinases (MMPs) are a family of proteins involved in a range of pathologies. Given that MMP broad-spectrum inhibition is associated with severe adverse effects, selectivity has become a priority in the design of MMP inhibitors, and is often achieved by targeting the variable S1' pocket. However, the specific characteristics of the S1' pocket that determine inhibitor selectivity are often not described and, in many cases, challenging to identify. In this review, we investigate the variability of the S1' pocket across the MMP family, and propose explanations for the selectivity of previously described inhibitors. These analyses provide valuable insights into how to design novel inhibitors selective for a given MMP.Copyright © 2019 Elsevier Ltd. All rights reserved.
  • Altres:

    Autor segons l'article: Gimeno, Aleix; Beltran-Debon, Raul; Mulero, Miguel; Pujadas, Gerard; Garcia-Vallve, Santiago
    Departament: Bioquímica i Biotecnologia
    Autor/s de la URV: Beltrán Debón, Raúl Alejandro / Garcia Vallve, Santiago / Gimeno Vives, Aleix / Mulero Abellán, Miguel / Pujadas Anguiano, Gerard
    Paraules clau: Amino acid sequence; Animals; Binding sites; Biological evaluation; Cancer; Chelating inhibitors; Crystal-structures; Design; Fragment-based discovery; Highly potent; Humans; Inflammatory-bowel-disease; Matrix metalloproteinase inhibitors; Matrix metalloproteinases; Mmp inhibition; Zinc-binding group
    Resum: Matrix metalloproteinases (MMPs) are a family of proteins involved in a range of pathologies. Given that MMP broad-spectrum inhibition is associated with severe adverse effects, selectivity has become a priority in the design of MMP inhibitors, and is often achieved by targeting the variable S1' pocket. However, the specific characteristics of the S1' pocket that determine inhibitor selectivity are often not described and, in many cases, challenging to identify. In this review, we investigate the variability of the S1' pocket across the MMP family, and propose explanations for the selectivity of previously described inhibitors. These analyses provide valuable insights into how to design novel inhibitors selective for a given MMP.Copyright © 2019 Elsevier Ltd. All rights reserved.
    Àrees temàtiques: Astronomia / física; Biochemistry & molecular biology; Biotecnología; Ciências biológicas i; Ciências biológicas ii; Ciências biológicas iii; Drug discovery; Interdisciplinar; Medicina i; Medicina ii; Medicina veterinaria; Pharmacology; Pharmacology & pharmacy; Química
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    Adreça de correu electrònic de l'autor: raul.beltran@urv.cat; gerard.pujadas@urv.cat; santi.garcia-vallve@urv.cat; miquel.mulero@urv.cat; aleix.gimeno@urv.cat; aleix.gimeno@urv.cat
    ISSN: 13596446
    Data d'alta del registre: 2025-03-22
    Versió de l'article dipositat: info:eu-repo/semantics/submittedVersion
    Enllaç font original: https://www.sciencedirect.com/science/article/abs/pii/S1359644619303411?via%3Dihub
    Referència a l'article segons font original: Drug Discovery Today. 25 (1): 38-57
    Referència de l'ítem segons les normes APA: Gimeno, Aleix; Beltran-Debon, Raul; Mulero, Miguel; Pujadas, Gerard; Garcia-Vallve, Santiago (2020). Understanding the variability of the S1' pocket to improve matrix metalloproteinase inhibitor selectivity profiles. Drug Discovery Today, 25(1), 38-57. DOI: 10.1016/j.drudis.2019.07.013
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    DOI de l'article: 10.1016/j.drudis.2019.07.013
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2020
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Biochemistry & Molecular Biology,Drug Discovery,Pharmacology,Pharmacology & Pharmacy
    Amino acid sequence
    Animals
    Binding sites
    Biological evaluation
    Cancer
    Chelating inhibitors
    Crystal-structures
    Design
    Fragment-based discovery
    Highly potent
    Humans
    Inflammatory-bowel-disease
    Matrix metalloproteinase inhibitors
    Matrix metalloproteinases
    Mmp inhibition
    Zinc-binding group
    Astronomia / física
    Biochemistry & molecular biology
    Biotecnología
    Ciências biológicas i
    Ciências biológicas ii
    Ciências biológicas iii
    Drug discovery
    Interdisciplinar
    Medicina i
    Medicina ii
    Medicina veterinaria
    Pharmacology
    Pharmacology & pharmacy
    Química
    13596446
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