Literature DB >> 181084

On the location of active serines of membrane acetylcholinesterase studied by the ESR method.

M Sentjurc, A Stalc, A O Zupancic.   

Abstract

1. An attempt was made to find out the causes of the discrepancy between the ESR spectra of membrane acetylcholinesterase (EC 3.1.1.7) obtained by Morrisett and co-workers and those obtained by the present authors. 2. In order to see whether the discrepancy was due to the different spin-labeling procedures, the same membrane acetylcholinesterase preparations were spin-labeled with the same compound, using the two different spin-labeling procedures. The enzyme activity was determined with pH-static titration and the ESR spectra recorded. 3. It was found that after spin-labeling according to Morrisett and co-workers, there were from 10-100 times more spin-label molecules bound to the enzyme preparations than there were active serines in them. 4. Using the method of Morrisett and co-workers, the majority of spin-label molecules was found to be bound to sites outside the active serines whereas the spin-labeling procedures of the present authors proved to be selective for active serines; the discrepancy in ESR spectra is explained.

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Year:  1976        PMID: 181084     DOI: 10.1016/0005-2744(76)90229-1

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


  2 in total

1.  Comparative study on the therapeutic ultrasound effects on erythrocyte membrane-bound and free acetylcholinesterase.

Authors:  F I Braginskaya; O M Zorina
Journal:  Radiat Environ Biophys       Date:  1987       Impact factor: 1.925

2.  Allosteric effects of phenyltrimethylammonium and propidium on acetylcholinesterase active site.

Authors:  A Stalc; M Sentjurc; S Pecar
Journal:  Pflugers Arch       Date:  1996       Impact factor: 3.657

  2 in total

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