Pregled bibliografske jedinice broj: 15718
Reversible inhibition of acetylcholinesterase and butyrylcholinesterase by 4,4-bipyridine and by a coumarin derivative
Reversible inhibition of acetylcholinesterase and butyrylcholinesterase by 4,4-bipyridine and by a coumarin derivative // Chemico-biological interactions, 119-120 (1999), 119-128 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 15718 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Reversible inhibition of acetylcholinesterase and butyrylcholinesterase by 4,4-bipyridine and by a coumarin derivative
(Reversible inhibition of acetylcholinesterase and butyrylcholinesterase by 4,4-bipyridine and by coumarin derivative)
Autori
Simeon-Rudolf, Vera ; Kovarik, Zrinka ; Radić, Zoran ; Reiner, Elsa
Izvornik
Chemico-biological interactions (0009-2797) 119-120
(1999);
119-128
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
acetylcholinesterase; butyrylcholinesterase; 4;4-bipyridine; coumarin derivative; reversible inhibition; molecular modelling
Sažetak
Inhibition of recombinant mouse wild type AChE (EC 3.1.1.7) and BChE (EC 3.1.1.8), and AChE peripheral site-directed mutants and human serum BChE variants by 4,4'-bipyridine (4,4'-BP) and the coumarin derivative 3-chloro-7-hydroxy-4-methylcoumarin (CHMC) was studied. The enzyme activity was measured with acetylthiocholine as substrate. Enzyme-inhibitor dissociation constants for the catalytic and peripheral sites were evaluated from the apparent dissociation constants as a function of the substrate concentration. Inhibition by 4,4'-BP of AChE , BChE and the AChE mutant Y72N/Y124Q/W286A, was consistent with inhibitor binding to both catalytic and peripheral sites. The dissociation constants for the peripheral site were about 3.5-times higher than for the catalytic site.The competition between CHMC and substrate displayed two binding sites on the AChE mutants Y72N, Y124Q, W286A and W286R, and on the atypical and fluoride-resistant BChE variants. The dissociation constants for the peripheral site were on average two-times higher than for the catalytic site. CHMC displayed binding only to the catalytic site of Y72N/Y124Q/W286A mutant and only to the peripheral site of w.t. AChE and the human usual BChE. Modelling of the 4,4'-BP and CHMC binding to wild type mouse AChE substantiated the difference between the inhibitors in their mode of binding which was revealed in the kinetic studies.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
00220104
Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb
Citiraj ovu publikaciju:
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
- MEDLINE
Uključenost u ostale bibliografske baze podataka::
- Biological Abstracts
- Excerpta medica
- Chem. Abstracts