Abstract |
We have used site-directed mutagenesis and molecular modeling to investigate the inactivation of an invertebrate acetylcholinesterase (AChE), ChE2 from amphioxus, by the sulfhydryl reagents 5,5'-dithiobis(2-nitrobenzoic acid) ( DTNB) and N-ethylmaleimide (NEM), creating various mutants, including C310A and C466A, and the double mutants C310A/C466A and C310A/F312I, to assess the relative roles of the two cysteines and a proposal that the increased rate of inactivation in the F312I mutant is due to increased access to Cys310. Our results suggest that both cysteines may be involved in inactivation by sulfhydryl reagents, but that the cysteine in the vicinity of the acyl pocket is more accessible. We speculate that the inactivation of aphid AChEs by sulfhydryl reagents is due to the presence of a cysteine homologous to Cys310. We also investigated the effects of various reversible cholinergic ligands, which bind to different subsites of the active site of the enzyme, on the rate of inactivation by DTNB of wild type ChE2 and ChE2 F312I. For the most part the inhibitors protect the enzymes from inactivation by DTNB. However, a notable exception is the peripheral site ligand propidium, which accelerates inactivation in the wild type ChE2, but retards inactivation in the F312I mutant. We propose that these opposing effects are the result of an altered allosteric signal transduction mechanism in the F312I mutant compared to the wild type ChE2.
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Authors | Leo Pezzementi, Melissa Rowland, Matthew Wolfe, Igor Tsigelny |
Journal | Invertebrate neuroscience : IN
(Invert Neurosci)
Vol. 6
Issue 2
Pg. 47-55
(Jun 2006)
ISSN: 1354-2516 [Print] Germany |
PMID | 16586114
(Publication Type: Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Amphibian Proteins
- Cholinesterase Inhibitors
- Sulfhydryl Reagents
- Dithionitrobenzoic Acid
- cholinesterase 2
- Cholinesterases
- Cysteine
- Ethylmaleimide
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Topics |
- Amphibian Proteins
(metabolism)
- Animals
- COS Cells
(drug effects, metabolism)
- Catalytic Domain
(drug effects)
- Chlorocebus aethiops
- Cholinesterase Inhibitors
(pharmacology)
- Cholinesterases
(metabolism)
- Cysteine
(metabolism)
- Dithionitrobenzoic Acid
(pharmacology)
- Enzyme Activation
(drug effects)
- Ethylmaleimide
(pharmacology)
- Inhibitory Concentration 50
- Models, Molecular
- Mutagenesis, Site-Directed
(methods)
- Sequence Alignment
- Sulfhydryl Reagents
(pharmacology)
- Time Factors
- Transfection
(methods)
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