Atomic-level mechanisms of abnormal activation in NRAS oncogenes from two dimensional free energy landscapes

The NRAS-mutant subset of melanoma is one of the most aggressive and lethal types associated with poor overall survival. Unfortunately, a low understanding of the NRAS-mutant dynamic behavior has lead to the lack of clinically approved therapeutic agents able to directly target NRAS oncogenes. In th...

Descripción completa

Detalles Bibliográficos
Autores: Hu, Zheyao, Martí Rabassa, Jordi|||0000-0002-3721-9634
Tipo de recurso: artículo
Fecha de publicación:2025
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/425634
Acceso en línea:https://hdl.handle.net/2117/425634
https://dx.doi.org/10.1039/D4NR03372H
Access Level:acceso abierto
Palabra clave:Oncogenes
NRAS oncogenes
well-tempered metadynamics
free energy surfaces
Oncogens
Àrees temàtiques de la UPC::Enginyeria química
Àrees temàtiques de la UPC::Ciències de la salut
Descripción
Sumario:The NRAS-mutant subset of melanoma is one of the most aggressive and lethal types associated with poor overall survival. Unfortunately, a low understanding of the NRAS-mutant dynamic behavior has lead to the lack of clinically approved therapeutic agents able to directly target NRAS oncogenes. In this work, accurate local structures of NRAS and its mutants have been fully explored through the corresponding free energy surfaces obtained by microsecond scale well-tempered metadynamics simulations. Free energy calculations are crucial to reveal the precise mechanisms of Q61 mutations at the atomic level. Considering specific atom-atom distances and angles as appropriate reaction coordinates, we have obtained free energy surfaces revealing local and global minima together with their main transitions states, unveiling the mechanisms of abnormal NRAS activation from atomic-level and quantitatively analyzing the corresponding stable states. This will help to advance in our understanding of the basic mechanisms of NRAS mutations, offering new opportunities for the design of potential inhibitors.