Structural consequences of the polymorphism Q223R in the human leptin receptor: A molecular dynamics study

Jonathan P. Carrillo-Vázquez, Brenda Chimal-Vega, Beatriz Zamora-López, Laurence A. Marchat, Claudia G. Benítez-Cardoza, César A.S. Reyes-López, Absalom Zamorano-Carrillo

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Leptin Receptor (LEPR) is a component of a signaling pathway related to appetite and energy expenditure. Single Nucleotide Polymorphisms (SNP) of Leptin receptor gene (lepr) have been proposed as possible modulator of adipose tissue and body weight. The main phenomenological consequence reported of these SNPs is the modulation of the LEP-LEPR interaction promoting the weight gain. Particularly, Q223R polymorphism has been associated with human obesity in some populations. In this work, we analyze the structural effects of Q223R substitution in a model of the extracellular region of LEPR comparing the stability between LEPR-Q and its Q223R variant (rs1137101) by Molecular Dynamics (MD) simulations. These results showed different behavior between both molecules after one nanosecond (ns) of simulation and significant differences in the secondary structure content were evidenced.

Original languageEnglish
Pages (from-to)239-248
Number of pages10
JournalAmerican Journal of Agricultural and Biological Science
Volume8
Issue number3
DOIs
StatePublished - 23 Sep 2013

Keywords

  • Homology modeling
  • Leptin Receptor
  • Molecular dynamics
  • Obesity
  • Polymorphism

Fingerprint

Dive into the research topics of 'Structural consequences of the polymorphism Q223R in the human leptin receptor: A molecular dynamics study'. Together they form a unique fingerprint.

Cite this