| Full text | |
| Author(s): |
de Carvalho, Daniella Romano
[1]
;
Ximenes, Valdecir Farias
[2]
;
Groppo, Milton
[3]
;
Cardoso, Carmen Lucia
[1]
Total Authors: 4
|
| Affiliation: | [1] Univ Sao Paulo, Fac Filosofia Ciencias & Letras Ribeirao Preto, Dept Quim, Grp Cromatog Bioafinidade & Prod Nat, BR-14040901 Ribeirao Preto, SP - Brazil
[2] Univ Estadual Paulista, Fac Ciencias, Dept Quim, BR-17033360 Bauru, SP - Brazil
[3] Univ Sao Paulo, Fac Filosofia Ciencias & Letras Ribeirao Preto, Dept Biol, BR-14040901 Ribeirao Preto, SP - Brazil
Total Affiliations: 3
|
| Document type: | Journal article |
| Source: | Journal of Pharmaceutical and Biomedical Analysis; v. 199, MAY 30 2021. |
| Web of Science Citations: | 0 |
| Abstract | |
Human tissue kallikreins (KLKs) are serine proteases involved in various physiological and pathological conditions, including cancer and neurological disorders. These enzymes constitute attractive drug targets, which has stimulated the search for new KLK inhibitors. In this study, we have covalently immobilized porcine pancreas KLK on an NHS-activated Sepharose matrix, to obtain KLK-Sepharose-NHS. The immobilized enzyme showed high recovered activity and maintained the ability of free KLK to recognize the synthetic substrate Z-Phe-Arg-AMC (K-Mapp = 10.3 +/- 0.9 mu M). As proof of concept, we used leupeptin as a reference inhibitor to perform inhibition studies for KLK-Sepharose-NHS and to determine the halfmaximal inhibitory concentration (IC50 = 0.13 +/- 0.01 mu M), the inhibition constant (K-i = 0.06 mu M), and the leupeptin inhibition mechanism. We evaluated several complex matrixes (plant crude extract) by the same bioassay, to demonstrate their applicability. The species Solanum lycocarpum, Stryphnodendron adstringens, and Psychotria carthagenensis gave the best results. KLK-Sepharose-NHS was fully active after six consecutive reaction cycles and retained about 60 % of its initial activity after being used for at least five months, so the bioassay developed herein is a promising strategy to screen and to identify KLK ligands. (C) 2021 Elsevier B.V. All rights reserved. (AU) | |
| FAPESP's process: | 16/06260-2 - Integrative systematic studies in Neotropical families, with emphasis on Rutaceae, Asteraceae and Rubiaceae |
| Grantee: | Milton Groppo Júnior |
| Support Opportunities: | Regular Research Grants |
| FAPESP's process: | 14/50249-8 - Green chemistry: sustainable synthetic methods employing benign solvents, safer reagents, and bio-renewable feedstock |
| Grantee: | Arlene Gonçalves Corrêa |
| Support Opportunities: | Research Grants - Research Centers in Engineering Program |
| FAPESP's process: | 19/05363-0 - Enzyme ligand screening: an on-flow approach via LC-MS/MS |
| Grantee: | Carmen Lúcia Cardoso |
| Support Opportunities: | Regular Research Grants |