Molecular Dynamics of the Peroxisome Proliferator -Activated Receptor: Association with Ligands and Coregulatory Proteins

• Grant number: 11/22735-7
• Support Opportunities: Scholarships in Brazil - Doctorate
• Start date: March 01, 2012
• End date: August 31, 2015
• Field of knowledge: Physical Sciences and Mathematics - Chemistry - Physical-Chemistry
• Principal Investigator: Munir Salomao Skaf
• Grantee: Melina Mottin
• Host Institution: Instituto de Química (IQ). Universidade Estadual de Campinas (UNICAMP). Campinas , SP, Brazil

Abstract

The Peroxisome Proliferator Activated Receptors gamma (PPAR gamma) is an important nuclear receptor which enhances insulin sensitivity, regulates the levels of plasma glucose and catches/stores lipids in peripheral tissues. Thus, the PPAR gamma consists of a molecular target for developing new drugs for treating type 2 diabetes. Among the ligands of this receptor, the full agonists, cause undesirable side effects such as weight gain, edema and congestive heart failure, although they reduce systemic insulin resistance. Therefore, partial agonists are interesting alternatives, because they retain the therapeutic effects of insulin sensitization without presenting the typical side effects of full agonists. Recent studies show that some structural characteristics are important for the receptor ligand-specific activation. One of these auxiliary factors of the activation is related to the phosphorylation of a serine of the receptor mediated by a protein kinase, CDK5. This is a very promising subject, as it allows integrating PPAR gamma interaction with another protein, CDK5, enabling a global view of the system. Our main objectives in this project aim to understand the molecular mechanisms involved in the phosphorylation reaction of S245 by cdk5 and understand how different ligands can inhibit more (or less) effectively the phosphorylation of this residue. For that goal, we propose using molecular dynamics simulations and hybrid quantum-classical simulations (QM / MM, Quantum Mechanics-Molecular Mechanics) to investigate PPARgamma and its association to Cdk5 and the effect of ligands on this enzyme-protein association.

Scientific publications

(The scientific publications listed on this page originate from the Web of Science or SciELO databases. Their authors have cited FAPESP grant or fellowship project numbers awarded to Principal Investigators or Fellowship Recipients, whether or not they are among the authors. This information is collected automatically and retrieved directly from those bibliometric databases.)

MOTTIN, MELINA; SOUZA, PAULO C. T.; SKAF, MUNIR S.. Molecular Recognition of PPAR gamma by Kinase Cdk5/p25: Insights from a Combination of Protein-Protein Docking and Adaptive Biasing Force Simulations. Journal of Physical Chemistry B, v. 119, n. 26, p. 8330-8339, JUL 2 2015. (13/08293-7, 11/22735-7, 12/24750-6)

MOTTIN, MELINA; SOUZA, PAULO C. T.; RICCI, CLARISSE G.; SKAF, MUNIR S.. CHARMM Force Field Parameterization of Peroxisome Proliferator-Activated Receptor gamma Ligands. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v. 18, n. 1, JAN 2017. (12/24750-6, 11/22735-7, 13/08293-7)

Academic Publications

(References retrieved automatically from State of São Paulo Research Institutions)

MOTTIN, Melina. Molecular dynamics of the peroxissome proliferator-activated receptor gamma: association with ligands and coregulatory proteins. 2015. Doctoral Thesis - Universidade Estadual de Campinas (UNICAMP). Instituto de Química Campinas, SP.