Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/36988
Title: Heparin Modulates the Endopeptidase Activity of Leishmania mexicana Cysteine Protease Cathepsin L-Like rCPB2.8
Authors: Judice, Wagner A. S.
Manfredi, Marcella A.
Souza, Gerson P.
Sansevero, Thiago M.
Almeida, Paulo C. [UNIFESP]
Shida, Claudio S. [UNIFESP]
Gesteira, Tarsis F.
Juliano, Luiz [UNIFESP]
Westrop, Gareth D.
Sanderson, Sanya J.
Coombs, Graham H.
Tersariol, Ivarne Luis dos Santos [UNIFESP]
Univ Mogi das Cruzes
Universidade Federal de São Paulo (UNIFESP)
Cincinnati Childrens Hosp Med Ctr
Univ Strathclyde
Issue Date: 21-Nov-2013
Publisher: Public Library Science
Citation: Plos One. San Francisco: Public Library Science, v. 8, n. 11, 12 p., 2013.
Abstract: Background: Cysteine protease B is considered crucial for the survival and infectivity of the Leishmania in its human host. Several microorganism pathogens bind to the heparin-like glycosaminoglycans chains of proteoglycans at host-cell surface to promote their attachment and internalization. Here, we have investigated the influence of heparin upon Leishmania mexicana cysteine protease rCPB2.8 activity.Methodology/Principal Findings: the data analysis revealed that the presence of heparin affects all steps of the enzyme reaction: (i) it decreases 3.5-fold the k(1) and 4.0-fold the k(-1), (ii) it affects the acyl-enzyme accumulation with pronounced decrease in k(2) (2.7-fold), and also decrease in k(3) (3.5-fold). the large values of triangle G = 12 kJ/mol for the association and dissociation steps indicate substantial structural strains linked to the formation/dissociation of the ES complex in the presence of heparin, which underscore a conformational change that prevents the diffusion of substrate in the rCPB2.8 active site. Binding to heparin also significantly decreases the alpha-helix content of the rCPB2.8 and perturbs the intrinsic fluorescence emission of the enzyme. the data strongly suggest that heparin is altering the ionization of catalytic (Cys(25))-S-/(His(163))-Im(+) H ion pair of the rCPB2.8. Moreover, the interaction of heparin with the N-terminal pro-region of rCPB2.8 significantly decreased its inhibitory activity against the mature enzyme.Conclusions/Significance: Taken together, depending on their concentration, heparin-like glycosaminoglycans can either stimulate or antagonize the activity of cysteine protease B enzymes during parasite infection, suggesting that this glycoconjugate can anchor parasite cysteine protease at host cell surface.
URI: http://repositorio.unifesp.br/handle/11600/36988
ISSN: 1932-6203
Other Identifiers: http://dx.doi.org/10.1371/journal.pone.0080153
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