Literature DB >> 241402

Reactivation and aging of diphenyl phosphoryl acetylcholinesterase.

J A Maglothin, P Wins, I B Wilson.   

Abstract

Acetylcholinesterase (acetylcholine hydrolase, EC 3.1.1.7) is readily in hibited by 10(-5) M diphenylphosphorochloridate even though the inhibitor hydrolyzes in a few seconds. The fluoridate is a much weaker inhibitor. The inhibited enzyme, diphenyl phosphoryl enzyme spontaneously recovers only about 50% of its activity with a half time of about 17 min at pH 7.0 and 6 min at pH 8.0. The fact that only 50% of the original activity returns is due to aging. The rates of reactivation and aging can be very greatly increased by a few percent of an organic solvent. Depending on the solvent even 1% may increase the rates by a factor of 5 or 6. The highest increase in rate was 70-fold. Quaternary NH+4 also increases the rates. Organic solvents and NH+4 also accelerate the reactivation of the much more stable diethyl phosphoryl enzyme derivative.

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Year:  1975        PMID: 241402     DOI: 10.1016/0005-2744(75)90066-2

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  4 in total

1.  Kinetics of protein modification, and/or enzyme inactivation, reactions by an unstable modifying agent.

Authors:  E T Rakitzis
Journal:  Biochem J       Date:  1987-09-15       Impact factor: 3.857

Review 2.  Kinetics of protein modification reactions.

Authors:  E T Rakitzis
Journal:  Biochem J       Date:  1984-01-15       Impact factor: 3.857

3.  Kinetics of irreversible enzyme inhibition by an unstable inhibitor.

Authors:  E T Rakitzis
Journal:  Biochem J       Date:  1981-11-01       Impact factor: 3.857

4.  Formation of an unstable covalent intermediate during the inhibition of electric-eel acetylcholinesterase with 1,3,2-dioxaphosphorinane 2-oxides.

Authors:  Y Ashani; H Leader
Journal:  Biochem J       Date:  1979-03-01       Impact factor: 3.857

  4 in total

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