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Correlation of neuropathy target esterase activity with specific tritiated di-isopropyl phosphorofluoridate-labelled proteins.
- Source :
-
The Biochemical journal [Biochem J] 1989 Jan 01; Vol. 257 (1), pp. 109-16. - Publication Year :
- 1989
-
Abstract
- Neuropathy target esterase (NTE) is a membrane-bound carboxylesterase activity that has been proposed as the target site for initiation of organophosphate-induced delayed neuropathy. This activity is identified by its resistance to treatment with Paraoxon and sensitivity to co-incubation with Paraoxon and Mipafox. Sucrose-density-gradient centrifugation of membrane-associated proteins isolated from chick-embryo brains identified three proteins, Mr 161,000, 116,500 and 103,000, that were labelled with [3H]di-isopropyl phosphorofluoridate in an NTE-like manner and that co-migrated with NTE. The 161,000-Mr and 116,500-Mr proteins were identified in both adult and embryo brain. One or both of these proteins may therefore contribute to the activity defined as NTE. In addition, a 61,000-Mr protein was identified that does not comigrate with NTE, but that was labelled with [3H]di-isopropyl phosphorofluoridate in a Paraoxon-resistant and Mipafox-sensitive manner. The effect of Mipafox on labelling, however, was reversibly blocked by co-incubation with Paraoxon. This protein, therefore, is not NTE, but has the necessary inhibitor-sensitivity to be the target site for organophosphate-induced delayed neuropathy.
- Subjects :
- Animals
Brain enzymology
Carboxylic Ester Hydrolases antagonists & inhibitors
Carboxylic Ester Hydrolases isolation & purification
Centrifugation, Density Gradient
Chick Embryo
Isoflurophate metabolism
Microsomes enzymology
Carboxylic Ester Hydrolases metabolism
Isoflurophate analogs & derivatives
Membrane Proteins metabolism
Paraoxon metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0264-6021
- Volume :
- 257
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- The Biochemical journal
- Publication Type :
- Academic Journal
- Accession number :
- 2920006
- Full Text :
- https://doi.org/10.1042/bj2570109