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Synthesis and studies of peptides and analogues involved principally in the renin-angiotensin and kallikrein-kinin system

Abstract

Since we belong to one of the few research groups that not only synthesizes peptides, but has also endeavored to refine this methodology, we have been able to acquire in the last decades, a good level of autonomy in obtaining this relevant class of macromolecules. Peptide analogues have been produced by different strategies, including the use of paramagnetic aminoacids, allowing us good lines of diversification in our research. Based on these considerations, we decided in the present project, to propose a broader line of research and integrated by ten sub-items, weighted principally towards the important physiological systems, renin-angiotensin and kallikrein-kinin. Some peptides present in these systems such as angiotensins, bradykinin and others, together with their analogues containing various alterations, principally of the non-natural type, in their structures, will be examined. The receptors involved in these systems will also be evaluated in different ways, ranging from experiments of site-directed mutations to studies of the difficulties of synthesis, purification and conformational analysis of some of their transmembranar hydrophobic fragments. In addition to classic investigation of the structure-function type, others such as the effect of radiations and of proteolytic enzymes on their structures, as well as the possibility of participation in tumoral processes, will also involve these selected peptides. Complementing these essentially more biological studies, other investigations apparently dissociated from the central theme will also be developed, since all will be inserted, in one way or another, into our continual effort to learn the Chemistry and Physico-Chemistry of peptides. (AU)

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Scientific publications (5)
(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
G PROTEIN-COUPLED RECEPTORS, PT B. Web of Science Citations: 0.
MARTIN, RENAN P.; FILIPPELLI-SILVA, RAFAEL; RODRIGUES, ELIETE S.; NAKAIE, CLOVIS R.; SHIMUTA, SUMA I. A fluorimetric binding assay for angiotensin II and kinin receptors. JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, v. 79, p. 55-59, MAY-JUN 2016. Web of Science Citations: 0.
GARCIA MOLINA WOLGIEN, MARIA DEL CARMEN; COTRIM GUERREIRO DA SILVA, ISMAEL DALE; PINTO NAZARIO, AFONSO CELSO; NAKAIE, CLOVIS RIUCHE; ALVES CORREA-NORONHA, SILVANA APARECIDA; RIBEIRO DE NORONHA, SAMUEL MARCOS; FACINA, GIL. Genetic Association Study of Angiotensin II Receptor Types 1 (A168G) and 2 (T1247G and A5235G) Polymorphisms in Breast Carcinoma among Brazilian Women. BREAST CARE, v. 9, n. 3, p. 176-181, 2014. Web of Science Citations: 5.
VIEIRA, JOAO P. F.; POLETTI, ERICK F.; VIEIRA, RENATA F. F.; VEREDAS, VINICIUS; SANTANA, CESAR C.; NAKAIE, CLOVIS R. Alternative and Simple Normal-Phase HPLC Enantioseparation of a Chiral Amino Acid-Type Spin Label Derivative. Journal of the Brazilian Chemical Society, v. 24, n. 11, p. 1840-1845, Nov. 2013. Web of Science Citations: 0.
BARROS, ALEXANDRE J.; ITO, CHRISTIAN M.; MAKINO, ELAINE N.; CEMBRANELLI, FERNANDO A. M.; MORAES, FRANCISCO C.; SOUZA, SINVAL E. G.; OLIVEIRA, LAERTE; SHIMUTA, SUMA I.; NAKAIE, CLOVIS R. Factors regulating tachyphylaxis triggered by N-terminal-modified angiotensin II analogs. Biological Chemistry, v. 390, n. 12, p. 1265-1270, DEC 2009. Web of Science Citations: 1.

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