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Mutagenesis and new oximes enable reactivation of tabun-inhibited acetylcholinesterases (CROSBI ID 588005)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Kovarik, Zrinka ; Kalisiak, Jarosław ; Maček, Nikolina ; Katalinić, Maja ; Berend, Suzana ; Radić, Zoran ; Fokin, Valery V. ; Sharpless, Barry K. ; Taylor, Palmer Mutagenesis and new oximes enable reactivation of tabun-inhibited acetylcholinesterases // Book of Abstracts of the FEBS3+ Meeting ˝From molecules to life and back˝, Opatija, Hrvatska / Dumić, Jerka ; Kovarik, Zrinka ; Varljen, Jadranka (ur.). Rijeka: Hrvatsko Društvo za Biotehnologiju, 2012. str. 57-x

Podaci o odgovornosti

Kovarik, Zrinka ; Kalisiak, Jarosław ; Maček, Nikolina ; Katalinić, Maja ; Berend, Suzana ; Radić, Zoran ; Fokin, Valery V. ; Sharpless, Barry K. ; Taylor, Palmer

engleski

Mutagenesis and new oximes enable reactivation of tabun-inhibited acetylcholinesterases

Acetylcholinesterase (AChE, EC 3.1.1.7), an important enzyme in cholinergic neurotransmission, is the primary target of organophosphorus compounds (OP) like pesticides and nerve agents such as tabun. A library of new oximes was screened for the reactivation activity of tabun- inhibited human recombinant AChE. Fifty-three out of 100 oximes reactivated wild type AChE, but only 14 of them restored full activity. Within this series, it appears that an approximate distance equivalent to 8 methylenes between two quaternary nitrogens achieved an optimal level of AChE reactivation. The mutant, Y337A, at the choline binding site was reactivated by more than 80% with only 13 of the oximes. The most efficient reactivators of Y337A appeared to be 2PAM analogs, with maximal reactivation rate constants kmax up to 10 times faster than those determined for the most efficient reactivator of AChE w.t. Although introducing an additional mutation into the Y337A choline binding site in double mutant Y337A/F338A reduced the enhancement observed in the Y337A mutant, the most efficient Y337A/F338A reactivators also contained the 8 methylene equivalence between two quaternary nitrogens as found for the wild type. It seems that, on average, the modification of the active site in the double mutant compromised molecular recognition reflected in the Kox constant, but slightly improved the maximal reactivation rate constant kmax. Since all oximes were designed as reactivators of phosphorylated AChE, a limited reactivation capacity for related butyrylcholinesterase (BChE, EC 3.1.1.8) was expected. However, 37 oximes reactivated tabun- inhibited BChE more efficiently than 2PAM, and five reached maximal reactivation of 70 %. In addition, toxicity and antidotal studies with lead reactivators in mice showed significantly improved protective indexes in therapy upon tabun exposure compared to the standard antidote, 2PAM. Therefore, our findings offer a platform for further development of more potent congenic antidotes in tabun and related phosphoramidate exposure.

reactivation; mutants; oximes; tabun

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Podaci o prilogu

57-x.

2012.

nije evidentirano

objavljeno

978-953-95551-4-4

Podaci o matičnoj publikaciji

Book of Abstracts of the FEBS3+ Meeting ˝From molecules to life and back˝, Opatija, Hrvatska

Dumić, Jerka ; Kovarik, Zrinka ; Varljen, Jadranka

Rijeka: Hrvatsko Društvo za Biotehnologiju

Podaci o skupu

FEBS3+ meeting: From Molecules to life and back

pozvano predavanje

13.06.2012-16.06.2012

Opatija, Hrvatska

Povezanost rada

Kemija