Pregled bibliografske jedinice broj: 628051
From the laboratory to the field: cholinesterase phosphylation and its subsequent reactivation by oximes in correlation with temperature
From the laboratory to the field: cholinesterase phosphylation and its subsequent reactivation by oximes in correlation with temperature // 14th Medical Chemical Defence Conference 2013: Translation of experimental research for improved treatment of chemical warfare agent poisoning, Munchen, Njemačka, Programm
München, Njemačka, 2013. (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
From the laboratory to the field: cholinesterase phosphylation and its subsequent reactivation by oximes in correlation with temperature
Autori
Katalinić, Maja ; Šinko, Goran ; Kovarik, Zrinka ; Stojan, Jure
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
14th Medical Chemical Defence Conference 2013: Translation of experimental research for improved treatment of chemical warfare agent poisoning, Munchen, Njemačka, Programm
/ - , 2013
Skup
14th Medical Chemical Defence Conference 2013: Translation of experimental research for improved treatment of chemical warfare agent poisoning
Mjesto i datum
München, Njemačka, 23.04.2013. - 25.04.2013
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
thermodynamic characterization; reactivation; oximes
Sažetak
The importance of cholinesterases (AChE, EC 3.1.1.7 and BChE, EC 3.1.1.8) in maintaining the homeostasis of an organism has been investigated and presented ever since their discovery. Even now, many new roles for these enzymes are being considered and described. Since many of the in vitro experiments concerning cholinesterases are performed at a lower temperature than the physiological one, a translation of the obtained experimental results to in vivo conditions presents a great challenge. Namely, activity of cholinesterases as enzymes displays a certain temperature optimum, in other words, all kinetic parameters describing cholinesterase activity and their interactions with ligands are temperature dependent. We focused our study on the thermodynamic characterization of cholinesterase interactions with organophosphorus pesticides and nerve agents, and the subsequent reactivation of phosphylated cholinesterases by oximes. The threat of a misuse of these highly toxic organophosphorus compounds (OPs) is still widely present. On the other hand, oximes as antidotes are characterised as orphan drugs, which further raises a wide array of concerns that should be addressed even in the early phases of antidote development. Therefore, a critical view is required for in vitro obtained experimental results in this area of research. The main goal of our study was to define a temperature-correlated model of cholinesterase phosphylation as well as of oxime-assisted reactivation. Such a model could prove valuable for estimating kinetic data at a desired temperature, for example the physiological one, based on the experiments performed at more convenient temperatures. It would also ensure a better selection of compounds for in vivo experiments. Furthermore, knowing the manner in which the properties of cholinesterases alter within a temperature range could improve the development of cholinesterase-based agents for OP decontamination. Acknowledgment This work was supported by the Croatian-Slovenian bilateral project 2012-2013 (PIs: G. Šinko, J. Stojan).
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
022-0222148-2889 - Interakcije organofosfata, karbamata i određenih liganada s esterazama (Kovarik, Zrinka, MZOS ) ( CroRIS)
Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb