Human tissue kallikrein S-1 subsite recognition of non-natural basic amino acids

dc.contributor.authorMelo, R. L.
dc.contributor.authorPozzo, RCB
dc.contributor.authorPimenta, D. C.
dc.contributor.authorPerissutti, E.
dc.contributor.authorCaliendo, G.
dc.contributor.authorSantagada, V
dc.contributor.authorJuliano, L.
dc.contributor.authorJuliano, M. A.
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.contributor.institutionUniv Naples Federico II
dc.date.accessioned2016-01-24T12:31:23Z
dc.date.available2016-01-24T12:31:23Z
dc.date.issued2001-05-01
dc.description.abstractWe explored the unique substrate specificity of the primary S-1 subsite of human urinary kallikrein (hK1), which accepts both Phe and Arg, using internally quenched fluorescent peptides Abz-G-X-S-R-Q-EDDnp and Abz-G-F-S-P-F-X-S-S-R-P-B-EBBnp [Abz is o-aminobenzoic acid, EDDnp is N-(2,4-dinitrophenyl)ethylenediamine], which were based on the human kininogen sequence at the C-terminal region of bradykinin, Position X, which in natural sequence stands for Arg; received the following synthetic basic non-natural amino acids: 4-(aminomethyl)phenylalanine (Amf), 4-guanidine phenylalanine (Gnf), 4-(aminomethyl)-N-isopropylphenylala (Iaf), N-im-(dimethyl)histidine [H(2Me)], 3-pyridylalanine (Pya), 4-piperidinylalanine (Ppa), 4-(atninomethyl)cyclohexylalnnine (Ama), and 4-(aminocyclohexyl)alanine (Aca), Only Abz-F-Amf-S-R-Q-EDDnp and Abz-F-[H(2Me)]-S-R-B-EDDnp were efficiently hydrolyzed, and all others were resistant to hydrolysis. However, Abz-F-Ama-S-R-Q-EBDnp inhibited hK1 with a K-i of 50 nM with high specificity compared to human plasma kallikrein, thrombin, plasmin, and trypsin, the Abz-G-F-S-P-F-X-S-S-R-P-B-EDDnp series were more susceptible to hK1, although the peptides with Gnf, Ppa, and Ama were resistant to it. Unexpectedly, the peptides in which X is His, Lys, H(2Me), Amf, Iaf, Ppa, and Aca were cleaved at amino or at carboxyl sires of these amino acids, indicating that the S-1' subsite has significant preference for basic residues. Human plasma kallikrein did not hydrolyze any peptide of this series except the natural sequence where X is Arg. in conclusion, the Si subsite of hK1 accepts amino acids with combined basic anal aromatic side chain, although for the S-1-P-1 interaction the preference is for aliphatic and basic side chains.en
dc.description.affiliationUNIFESP, Escola Paulista Med, Dept Biofis, BR-04044020 São Paulo, Brazil
dc.description.affiliationUniv Naples Federico II, Dipartimento Chim Farmaceut & Tossicol, I-80131 Naples, Italy
dc.description.affiliationUnifespUNIFESP, Escola Paulista Med, Dept Biofis, BR-04044020 São Paulo, Brazil
dc.description.sourceWeb of Science
dc.format.extent5226-5232
dc.identifierhttp://dx.doi.org/10.1021/bi002003u
dc.identifier.citationBiochemistry. Washington: Amer Chemical Soc, v. 40, n. 17, p. 5226-5232, 2001.
dc.identifier.doi10.1021/bi002003u
dc.identifier.issn0006-2960
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/26546
dc.identifier.wosWOS:000168435100014
dc.language.isoeng
dc.publisherAmer Chemical Soc
dc.relation.ispartofBiochemistry
dc.rightsAcesso restrito
dc.titleHuman tissue kallikrein S-1 subsite recognition of non-natural basic amino acidsen
dc.typeArtigo
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