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Pregled bibliografske jedinice broj: 830373

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


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 (međunarodna recenzija, članak, znanstveni)


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

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

Izvornik
RSC Advances (2046-2069) 6 (2016); 83044-83052

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Dipeptidyl peptidase III ; guanidiniocarbonyl-pyrrole ; phenanthridine ; pyrene ; inhibitor

Sažetak
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.

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Biologija



POVEZANOST RADA


Projekt / tema
HRZZ-IP-2013-11-1477 - Višenamjensko očitavanje DNA / RNA sekundarne strukture molekularnim kemijskim senzorima (Ivo Piantanida, )
HRZZ-IP-2013-11-7235 - Povezanost fleksibilnosti, aktivnosti i strukture u porodici dipeptidil-peptidaza III (Sanja Tomić, )

Ustanove
Institut "Ruđer Bošković", Zagreb

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus


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