Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
izvor podataka: crosbi

Guanidiniocarbonyl-pyrrole -aryl conjugates as inhibitors of human dipeptidyl peptidase III: combined experimental and computational study (CROSBI ID 230941)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Matić, Josipa ; Šupljika, Filip ; Tir, Nora ; Piotrowski, Patryciusz ; Schmuck, Carsten ; Abramić, Marija ; Piantanida, Ivo ; Tomić, Sanja Guanidiniocarbonyl-pyrrole -aryl conjugates as inhibitors of human dipeptidyl peptidase III: combined experimental and computational study // RSC Advances, 6 (2016), 83044-83052. doi: 10.1039/c6ra16966j

Podaci o odgovornosti

Matić, Josipa ; Šupljika, Filip ; Tir, Nora ; Piotrowski, Patryciusz ; Schmuck, Carsten ; Abramić, Marija ; Piantanida, Ivo ; Tomić, Sanja

engleski

Guanidiniocarbonyl-pyrrole -aryl conjugates as inhibitors of human dipeptidyl peptidase III: combined experimental and computational study

Dipeptidyl peptidase III (DPP III) is a zinc dependant peptidase which catalyses hydrolysis of the second peptide bond from the N-termini of its substrates. DPP III is an enzyme of broad substrate specificity and it has been found in many organisms. It has been recognised in several processes of interest for the drug development like pain modulation and defence against oxidative stress. However, its fundamental physiological role is unknown and the specific inhibitors would be of significant help in identifying this role. In this work we combined experimental (UV/Vis, fluorimetry and microcalorimetry experiments) with molecular dynamic simulations to study binding of several newly designed and synthesised guanidiniocarbonyl-pyrrole -aryl conjugates to human DPP III. We found that new compounds bind with micromolar affinity to the enzyme and with various efficiency inhibit hydrolysis of Arg-Arg-2-naphthylamide, the standard synthetic substrate of DPP III. The molecular modelling study revealed multiple binding modes of the guanidiniocarbonyl-pyrrole -aryl conjugates into the active site of human DPP III. In order to elucidate which one is the most favourable we studied the molecular determinants for their binding to DPP III as well as their influence on protein structure. It seems that the main requirements for a good DPP III inhibitor is the bulky aryl-substituent and a linker of proper length and flexibility between it and guanidiniocarbonyl-pyrrole. The obtained results gave directions for future development and improvement of DPP III inhibitors.

dipeptidyl peptidase III ; guanidiniocarbonyl-pyrrole ; phenanthridine ; pyrene ; inhibitor

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

6

2016.

83044-83052

objavljeno

2046-2069

10.1039/c6ra16966j

Povezanost rada

Kemija, Biologija

Poveznice
Indeksiranost