Efficient hydrolysis of the chemical warfare nerve agent tabun by recombinant and purified human and rabbit serum paraoxonase 1
► Reporting for the first time that paraoxonase 1 (PON1) efficiently hydrolyzes tabun. ► Efficiency of tabun hydrolysis by PON1 was compared to that of sarin and soman. ► Demonstrate that hydrolysis of the nerve agents is PON1 specific. ► Evaluated retention of PON1 activity and 3-fold more hydrolys...
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Veröffentlicht in: | Biochemical and biophysical research communications 2010-12, Vol.403 (1), p.97-102 |
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Zusammenfassung: | ► Reporting for the first time that paraoxonase 1 (PON1) efficiently hydrolyzes tabun. ► Efficiency of tabun hydrolysis by PON1 was compared to that of sarin and soman. ► Demonstrate that hydrolysis of the nerve agents is PON1 specific. ► Evaluated retention of PON1 activity and 3-fold more hydrolysis of nerve agents. ► PON1 can be used as a universal bioscavenger against nerve agents.
Paraoxonase 1 (PON1) has been described as an efficient catalytic bioscavenger due to its ability to hydrolyze organophosphates (OPs) and chemical warfare nerve agents (CWNAs). It is the future most promising candidate as prophylactic medical countermeasure against highly toxic OPs and CWNAs. Most of the studies conducted so far have been focused on the hydrolyzing potential of PON1 against nerve agents, sarin, soman, and VX. Here, we investigated the hydrolysis of tabun by PON1 with the objective of comparing the hydrolysis potential of human and rabbit serum purified and recombinant human PON1. The hydrolysis potential of PON1 against tabun, sarin, and soman was evaluated by using an acetylcholinesterase (AChE) back-titration Ellman method. Efficient hydrolysis of tabun (100nM) was observed with ∼25–40mU of PON1, while higher concentration (80–250mU) of the enzyme was required for the complete hydrolysis of sarin (11nM) and soman (3nM). Our data indicate that tabun hydrolysis with PON1 was ∼30–60times and ∼200–260times more efficient than that with sarin and soman, respectively. Moreover, the catalytic activity of PON1 varies from source to source, which also reflects their efficiency of hydrolyzing different types of nerve agents. Thus, efficient hydrolysis of tabun by PON1 suggests its promising potential as a prophylactic treatment against tabun exposure. |
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ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1016/j.bbrc.2010.10.125 |