Theoretical models of staurosporine and analogs uncover detailed structural information in biological solution.


Journal

Journal of molecular graphics & modelling
ISSN: 1873-4243
Titre abrégé: J Mol Graph Model
Pays: United States
ID NLM: 9716237

Informations de publication

Date de publication:
Jan 2024
Historique:
received: 08 08 2023
revised: 12 10 2023
accepted: 12 10 2023
medline: 27 11 2023
pubmed: 6 11 2023
entrez: 3 11 2023
Statut: ppublish

Résumé

Staurosporine and its analogs (STA-analogs) are indolocarbazoles (ICZs) compounds able to inhibit kinase proteins in a non-specific way, while present antimicrobial and cytostatic properties. The knowledge of molecular features associated to the complexation, including the ligand shape in solution and thermodynamics of complexation, is substantial to the development of new bioactive ICZs with improved therapeutic properties. In this context, the empirical approach of GROMOS force field is able to accurately reproduce condensed phase physicochemical properties of molecular systems after parameterization. Hence, through parameterization under GROMOS force field and molecular simulations, we assessed STA-analogs dynamics in aqueous solution, as well as its interaction with water to probe conformational and structural features involved in complexation to therapeutic targets. The coexistence of multiple conformers observed in simulations, and confirmed by metadynamics calculations, expanding the conformational space knowledge of these ligands with potential implications in understanding the ligand conformational selection during complexation. Also, changes in availability to H-bonding concerning the different substituents and water can reflect on effects at complexation free energy due to variation at the desolvation energetic costs. Based on these results, we expect the obtained structural data provide systemic framework for rational chemical modification of STA-analogs.

Identifiants

pubmed: 37922640
pii: S1093-3263(23)00251-6
doi: 10.1016/j.jmgm.2023.108653
pii:
doi:

Substances chimiques

Staurosporine H88EPA0A3N
Ligands 0
Water 059QF0KO0R

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

108653

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Hugo Verli reports financial support was provided by Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPQ). Hugo Verli reports financial support was provided by Sistema Nacional de Processamento de Alto Desempenho (SINAPAD). Hugo Verli reports was provided by Fundação de Amparo a Pesquisa do Estado do Rio Grande do Sul (FAPERGS). Crisciele Fontana reports was provided by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES).

Auteurs

Crisciele Fontana (C)

Universidade Federal do Rio Grande do Sul, Centro de Biotecnologia, Av. Bento Gonçalves, 9500 (Caixa Postal 15005), Porto Alegre, CEP 91501-970, RS, Brazil.

João Luiz de Meirelles (JL)

Universidade Federal do Rio Grande do Sul, Centro de Biotecnologia, Av. Bento Gonçalves, 9500 (Caixa Postal 15005), Porto Alegre, CEP 91501-970, RS, Brazil.

Hugo Verli (H)

Universidade Federal do Rio Grande do Sul, Centro de Biotecnologia, Av. Bento Gonçalves, 9500 (Caixa Postal 15005), Porto Alegre, CEP 91501-970, RS, Brazil. Electronic address: hugoverli@gmail.com.

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Classifications MeSH