Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/348493
Type: Artigo
Title: Gaining ligand selectivity in thyroid hormone receptors via entropy
Author: Martínez, Leandro
Nascimento, Alessandro S.
Nunes, Fabio M.
Phillips, Kevin
Aparicio, Ricardo
Dias, Sandra Martha G.
Figueira, Ana Carolina M.
Lin, Jean H.
Nguyen, Phuong
Apriletti, James W.
Neves, Francisco A. R.
Baxter, John D.
Webb, Paul
Skaf, Munir S.
Polikarpov, Igor
Abstract: Nuclear receptors are important targets for pharmaceuticals, but similarities between family members cause difficulties in obtaining highly selective compounds. Synthetic ligands that are selective for thyroid hormone (TH) receptor β (TRβ) vs. TRα reduce cholesterol and fat without effects on heart rate; thus, it is important to understand TRβ-selective binding. Binding of 3 selective ligands (GC-1, KB141, and GC-24) is characterized at the atomic level; preferential binding depends on a nonconserved residue (Asn-331β) in the TRβ ligand-binding cavity (LBC), and GC-24 gains extra selectivity from insertion of a bulky side group into an extension of the LBC that only opens up with this ligand. Here we report that the natural TH 3,5,3′-triodothyroacetic acid (Triac) exhibits a previously unrecognized mechanism of TRβ selectivity. TR x-ray structures reveal better fit of ligand with the TRα LBC. The TRβ LBC, however, expands relative to TRα in the presence of Triac (549 Å3 vs. 461 Å3), and molecular dynamics simulations reveal that water occupies the extra space. Increased solvation compensates for weaker interactions of ligand with TRβ and permits greater flexibility of the Triac carboxylate group in TRβ than in TRα. We propose that this effect results in lower entropic restraint and decreases free energy of interactions between Triac and TRβ, explaining subtype-selective binding. Similar effects could potentially be exploited in nuclear receptor drug design
Subject: Mobilidade
Country: Estados Unidos
Editor: National Academy of Sciences
Rights: Fechado
Identifier DOI: 10.1073/pnas.0911024106
Address: https://www.pnas.org/content/106/49/20717
Date Issue: 2009
Appears in Collections:IQ - Artigos e Outros Documentos

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