Structural and thermodynamic analysis of thrombin:suramin interaction in solution and crystal phases
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
---|---|
Data(s) |
20/10/2012
20/10/2012
2009
|
Resumo |
Suramin is a hexasulfonated naphthylurea which has been recently characterized as a non-competitive inhibitor of human alpha-thrombin activity over fibrinogen, although its binding site and mode of interaction with the enzyme remain elusive. Here, we determined two X-ray structure of the thrombin: suramin complex, refined at 2.4 angstrom resolution. While a single thrombin: suramin complex was found in the asymmetric unit cell of the crystal, some of the crystallographic contacts with symmetrically related molecules are mediated by both the enzyme and the ligand. Molecular dynamics simulations with the 1:1 complex demonstrate a large rearrangement of suramin in the complex, but with the protein scaffold and the more extensive protein-ligand regions keep unchanged. Small-angle X-ray scattering measurements at high micromolar concentration demonstrate a suramin-induced dimerization of the enzyme. These data indicating a dissimilar binding mode in the monomeric and oligomeric states, with a monomeric, 1:1 complex to be more likely to exist at the thrombin physiological, nanomolar concentration range. Collectively, close understanding on the structural basis for interaction is given which might establish a basis for design of suramin analogues targeting thrombin. Crown Copyright (C) 2009 Published by Elsevier B.V. All rights reserved. Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) Nacional de Desenvolvimento Cientifico e Tecnologico Nacional de Desenvolvimento Cientifico e Tecnologico Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ) Fundacao de Amparo a Pesquisa do Estado do Rio de Janeiro Carlos Chagas Filho (FAPERJ) PRONEX, Brazilian Synchrotron Light Laboratory (LNLS) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Brazilian Synchrotron Light Laboratory (LNLS) Fundacao de Amparo a Pesquisa do Estado de SAO Paulo (FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) |
Identificador |
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, v.1794, n.6, p.873-881, 2009 1570-9639 http://producao.usp.br/handle/BDPI/29946 10.1016/j.bbapap.2009.03.011 |
Idioma(s) |
eng |
Publicador |
ELSEVIER SCIENCE BV |
Relação |
Biochimica Et Biophysica Acta-proteins and Proteomics |
Direitos |
restrictedAccess Copyright ELSEVIER SCIENCE BV |
Palavras-Chave | #Thrombin #Suramin #Crystallography #Molecular dynamic simulation #Small-angle X-ray scattering #HUMAN ALPHA-THROMBIN #PROTEIN CRYSTALLOGRAPHY BEAMLINE #PRO-ARG CHLOROMETHYLKETONE #X-RAY-SCATTERING #MOLECULAR-DYNAMICS #SURAMIN ANALOGS #BETA-LACTOGLOBULIN #HEPARIN #HEXOKINASE #BINDING #Biochemistry & Molecular Biology #Biophysics |
Tipo |
article original article publishedVersion |