Tritiated diisopropylfluorophosphate (DFP) was used to phosphorylate acetylcholinesterase (AChase) in the motor end plate of mouse sternomastoid muscle, and its distribution within the end plate was evaluated quantitatively by electron microscope radioautography. With the use of emulsion layers whose sensitivity to tritium had been calibrated, the density of AChase in different components of the end plate was calculated. The AChase was primarily localized (85%) in the junctional fold region. The concentration of AChase there was more than 20,000 active sites per cubic micron of tissue. The resolution of the technique was not sufficient to determine whether there was some AChase in the nerve end bulb; however, if there is any there, the concentration must be less than 10% of that at the junctional fold region.
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1 February 1967
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February 01 1967
ELECTRON MICROSCOPE RADIOAUTOGRAPHY AS A QUANTITATIVE TOOL IN ENZYME CYTOCHEMISTRY : I. The Distribution of Acetylcholinesterase at Motor End Plates of a Vertebrate Twitch Muscle
Miriam M. Salpeter
Miriam M. Salpeter
From the Department of Engineering Physics and Section of Neurobiology and Behavior, Cornell University, Ithaca, New York
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Miriam M. Salpeter
From the Department of Engineering Physics and Section of Neurobiology and Behavior, Cornell University, Ithaca, New York
Received:
July 29 1966
Online ISSN: 1540-8140
Print ISSN: 0021-9525
Copyright © 1967 by The Rockefeller University Press
1967
J Cell Biol (1967) 32 (2): 379–389.
Article history
Received:
July 29 1966
Citation
Miriam M. Salpeter; ELECTRON MICROSCOPE RADIOAUTOGRAPHY AS A QUANTITATIVE TOOL IN ENZYME CYTOCHEMISTRY : I. The Distribution of Acetylcholinesterase at Motor End Plates of a Vertebrate Twitch Muscle . J Cell Biol 1 February 1967; 32 (2): 379–389. doi: https://doi.org/10.1083/jcb.32.2.379
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