Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/214
Type: Artigo de periódico
Title: Structural basis of GC-1 selectivity for thyroid hormone receptor isoforms
Author: BLEICHER, Lucas
APARICIO, Ricardo
NUNES, Fabio M.
MARTINEZ, Leandro
DIAS, Sandra M. Gomes
FIGUEIRA, Ana Carolina Migliorini
SANTOS, Maria Auxiliadora Morim
VENTURELLI, Walter H.
SILVA, Rosangela da
DONATE, Paulo Marcos
NEVES, Francisco A. R.
SIMEONI, Luiz A.
BAXTER, John D.
WEBB, Paul
SKAF, Munir S.
POLIKARPOV, Igor
Abstract: Background: Thyroid receptors, TRa and TR beta, are involved in important physiological functions such as metabolism, cholesterol level and heart activities. Whereas metabolism increase and cholesterol level lowering could be achieved by TR beta isoform activation, TRa activation affects heart rates. Therefore, beta-selective thyromimetics have been developed as promising drug-candidates for treatment of obesity and elevated cholesterol level. GC-1 [ 3,5-dimethyl-4-(4'-hydroxy- 3'-isopropylbenzyl)-phenoxy acetic acid] has ability to lower LDL cholesterol with 600-to 1400-fold more potency and approximately two-to threefold more efficacy than atorvastatin (Lipitor(C)) in studies in rats, mice and monkeys. Results: To investigate GC-1 specificity, we solved crystal structures and performed molecular dynamics simulations of both isoforms complexed with GC-1. Crystal structures reveal that, in TRa Arg228 is observed in multiple conformations, an effect triggered by the differences in the interactions between GC-1 and Ser277 or the corresponding asparagine (Asn331) of TR beta. The corresponding Arg282 of TR beta is observed in only one single stable conformation, interacting effectively with the ligand. Molecular dynamics support this model: our simulations show that the multiple conformations can be observed for the Arg228 in TR alpha, in which the ligand interacts either strongly with the ligand or with the Ser277 residue. In contrast, a single stable Arg282 conformation is observed for TR beta, in which it strongly interacts with both GC-1 and the Asn331. Conclusion: Our analysis suggests that the key factors for GC-1 selectivity are the presence of an oxyacetic acid ester oxygen and the absence of the amino group relative to T(3). These results shed light into the beta-selectivity of GC-1 and may assist the development of new compounds with potential as drug candidates to the treatment of hypercholesterolemia and obesity.
Country: Inglaterra
Editor: BIOMED CENTRAL LTD
Citation: BMC STRUCTURAL BIOLOGY, v.8, 2008
Rights: aberto
Identifier DOI: 10.1186/1472-6807-8-8
Address: http://dx.doi.org/10.1186/1472-6807-8-8
http://apps.isiknowledge.com/InboundService.do?Func=Frame&product=WOS&action=retrieve&SrcApp=EndNote&UT=000254549600003&Init=Yes&SrcAuth=ResearchSoft&mode=FullRecord
Date Issue: 2008
Appears in Collections:IQ - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
art_BLEICHER_Structural_basis_of_GC-1_selectivity_for_thyroid_2008.pdfpublished version831.26 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.