dc.contributor | Univ Peruana Cayetano Heredia | |
dc.contributor | Inst Salud Carlos III | |
dc.contributor | Carlsberg Lab | |
dc.contributor | Univ Glasgow | |
dc.contributor | Universidade Federal de São Paulo (UNIFESP) | |
dc.creator | Lanfranco, Maria F. | |
dc.creator | Loayza-Muro, Raul | |
dc.creator | Clark, Daniel | |
dc.creator | Nunez, Regina | |
dc.creator | Zavaleta, Amparo I. | |
dc.creator | Jimenez, Maribel | |
dc.creator | Meldal, Morten | |
dc.creator | Coombs, Graham H. | |
dc.creator | Mottram, Jeremy C. | |
dc.creator | Izidoro, Mario [UNIFESP] | |
dc.creator | Juliano, Maria A. [UNIFESP] | |
dc.creator | Juliano, Luiz [UNIFESP] | |
dc.creator | Arevalo, Jorge | |
dc.date.accessioned | 2016-01-24T13:51:44Z | |
dc.date.available | 2016-01-24T13:51:44Z | |
dc.date.created | 2016-01-24T13:51:44Z | |
dc.date.issued | 2008-10-01 | |
dc.identifier | Molecular and Biochemical Parasitology. Amsterdam: Elsevier B.V., v. 161, n. 2, p. 91-100, 2008. | |
dc.identifier | 0166-6851 | |
dc.identifier | http://repositorio.unifesp.br/handle/11600/30944 | |
dc.identifier | 10.1016/j.molbiopara.2008.06.005 | |
dc.identifier | WOS:000259339400002 | |
dc.description.abstract | The cysteine proteinase B of Leishmania parasites is an important virulence factor. in this study we have expressed, isolated and characterized for the first time a recombinant CPB from Leishmania braziliensis, the causative agent of mucocutaneous leishmaniosis. the mature region of the recombinant CPB shares a high percentage identity with its Leishmania mexicana CPB2.8 (rCPB2.8 Delta CTE) counterpart (76.36%) and has identical amino acid residues at the S(1), catalytic triad and S'(1) subsites. Nevertheless, when the kinetics of substrate hydrolysis was measured using a combinatorial library of internally quenched fluorescent peptides based upon the lead sequence Abz-KLRSSKQ-EDDnp, significant differences were obtained. These results suggest that the differences in substrate utilization observed between the L. mexicana and L braziliensis CPs must be related to amino acid modifications outside the core of the active site cleft. Moreover, a potent inhibitor with Pro at P1 and high affinity for L. braziliensis recombinant CPB showed less affinity to L. mexicana CPB 2.8, which preferred Phe, Leu, and Asn at the same position. (c) 2008 Elsevier B.V. All rights reserved. | |
dc.language | eng | |
dc.publisher | Elsevier B.V. | |
dc.relation | Molecular and Biochemical Parasitology | |
dc.rights | http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy | |
dc.rights | Acesso restrito | |
dc.subject | Leishmania braziliensis | |
dc.subject | recombinant protease | |
dc.subject | cysteine protease B | |
dc.subject | enzyme kinetic parameters | |
dc.subject | fluorogenic peptides | |
dc.subject | peptide inhibitors | |
dc.title | Expression and substrate specificity of a recombinant cysteine proteinase B of Leishmania braziliensis | |
dc.type | Artigo | |