Literature DB >> 6870792

Intramolecular group transfer is a characteristic of neurotoxic esterase and is independent of the tissue source of the enzyme. A comparison of the aging behaviour of di-isopropyl phosphorofluoridate-labelled proteins in brain, spinal cord, liver, kidney and spleen from hen and in human placenta.

D G Williams.   

Abstract

Neurotoxic esterase activity was measured in homogenates of human placenta and hen brain, spinal cord, liver, kidney and spleen. The activity in liver comprised less than 20% of the Paraoxon-resistant esterases, but in the other tissues neurotoxic esterase accounted for over 50%. The same tissues were labelled with [3H]di-isopropyl phosphorofluoridate, and any isopropyl group transferred on to protein during 'aging' of the labelled enzymes (alkali-volatilizable tritium) was measured. No Paraoxon-sensitive labelled sites were found to age in this way in any tissue. In brain, the Paraoxon-resistant alkali-volatilizable-tritium-labelled sites correlated with the number of neurotoxic esterase labelled sites, indicating that 'aging' and isopropyl group transfer were 100% efficient. The site receiving the transferred isopropyl group was characterized by analysing the distribution of radiolabelled proteins on gel-filtration chromatography in the presence of SDS. In particulate preparations from each tissue, the protein-bound alkali-volatilizable tritium (transferred isopropyl group) was attached to a polypeptide of Mr 178 000. This same polypeptide also bore the isopropyl-phosphoryl group of neurotoxic esterase, indicating that aging of neurotoxic esterase is an intramolecular group transfer. The apparent turnover number for the enzyme (average 1.6 X 10(5) min-1) was approximately the same in each hen tissue, confirming that closely similar enzymes were present in brain, spinal cord, liver and spleen. The apparent turnover for the human enzyme was 1.8-fold higher than that for the hen enzyme. The concentration of the neurotoxic esterase phosphorylated subunit in brain, spinal cord, spleen, placenta and liver was 14.6, 3.8, 7.4, 3.3 and 3.8 pmol/g of tissue. The evidence indicated that neurotoxic esterase is present in each tissue except kidney, and that isopropyl group transfer on 'aging' occurs on this enzyme only. This process is an intramolecular transfer of the group within the same polypeptide.

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Year:  1983        PMID: 6870792      PMCID: PMC1154162          DOI: 10.1042/bj2090817

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  9 in total

1.  The reaction of chymotrypsin and diisopropylphosphorofluoridate. I. Isolation and analysis of diisopropylphosphoryl-peptides.

Authors:  R A OOSTERBAAN; P KUNST; J VAN ROTTERDAM; J A COHEN
Journal:  Biochim Biophys Acta       Date:  1958-03

Review 2.  Control mechanisms in the synthesis of saturated fatty acids.

Authors:  K Bloch; D Vance
Journal:  Annu Rev Biochem       Date:  1977       Impact factor: 23.643

3.  The primary biochemical lesion leading to the delayed neurotoxic effects of some organophosphorus esters.

Authors:  M K Johnson
Journal:  J Neurochem       Date:  1974-10       Impact factor: 5.372

4.  A phosphorylation site in brain and the delayed neurotoxic effect of some organophosphorus compounds.

Authors:  M K Johnson
Journal:  Biochem J       Date:  1969-02       Impact factor: 3.857

5.  Organophosphorus and other inhibitors of brain 'neurotoxic esterase' and the development of delayed neurotoxicity in hens.

Authors:  M K Johnson
Journal:  Biochem J       Date:  1970-12       Impact factor: 3.857

6.  Rapid aging of neurotoxic esterase after inhibition by di-isopropyl phosphorofluoridate.

Authors:  B Clothier; M K Johnson
Journal:  Biochem J       Date:  1979-02-01       Impact factor: 3.857

7.  Interaction of the hinge region of human immunoglobulin G with a murine lymphocyte membrane receptor. Relevance to the problem of antiglobulin induction in rheumatoid arthritis.

Authors:  P M Johnson; M Papamichail; C Gutierrez; E J Holborow
Journal:  Immunology       Date:  1975-05       Impact factor: 7.397

8.  Gel-electrophoretic identification of hen brain neurotoxic esterase, labelled with tritiated di-isopropyl phosphorofluoridate.

Authors:  D G Williams; M K Johnson
Journal:  Biochem J       Date:  1981-11-01       Impact factor: 3.857

9.  The delayed neurotoxic effect of some organophosphorus compounds. Identification of the phosphorylation site as an esterase.

Authors:  M K Johnson
Journal:  Biochem J       Date:  1969-10       Impact factor: 3.857

  9 in total
  8 in total

1.  Kinetics of substrate hydrolysis and inhibition by mipafox of paraoxon-preinhibited hen brain esterase activity.

Authors:  C D Carrington; M B Abou-Donia
Journal:  Biochem J       Date:  1986-06-01       Impact factor: 3.857

2.  Effect of over-expression of neuropathy target esterase on mammalian cell proliferation.

Authors:  P-A Chang; Ch-Y Liu; R Chen; Y-J Wu
Journal:  Cell Prolif       Date:  2006-10       Impact factor: 6.831

3.  The role of cell cycle-dependent neuropathy target esterase in cell proliferation.

Authors:  Ping-An Chang; Yu-ying Chen; Wen-zhen Qin; Ding-Xin Long; Yi-Jun Wu
Journal:  Mol Biol Rep       Date:  2010-03-21       Impact factor: 2.316

Review 4.  Prophylaxis and the mechanism for the initiation of organophosphorous compound-induced delayed neurotoxicity.

Authors:  C D Carrington
Journal:  Arch Toxicol       Date:  1989       Impact factor: 5.153

5.  Functional pathways altered after silencing Pnpla6 (the codifying gene of neuropathy target esterase) in mouse embryonic stem cells under differentiation.

Authors:  David Pamies; Eugenio Vilanova; Miguel A Sogorb
Journal:  In Vitro Cell Dev Biol Anim       Date:  2013-10-19       Impact factor: 2.416

6.  Characterization of [3H]di-isopropyl phosphorofluoridate-binding proteins in hen brain. Rates of phosphorylation and sensitivity to neurotoxic and non-neurotoxic organophosphorus compounds.

Authors:  C D Carrington; M B Abou-Donia
Journal:  Biochem J       Date:  1985-06-15       Impact factor: 3.857

7.  CREB is required for cAMP/PKA signals upregulating neuropathy target esterase expression.

Authors:  Jia-Xiang Chen; Yi-Jun Wu
Journal:  DNA Cell Biol       Date:  2013-03-21       Impact factor: 3.311

8.  Target size of neurotoxic esterase and acetylcholinesterase as determined by radiation inactivation.

Authors:  C D Carrington; D J Fluke; M B Abou-Donia
Journal:  Biochem J       Date:  1985-11-01       Impact factor: 3.857

  8 in total

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