The proteome of the presynaptic active zone from mouse brain.

Mol Cell Neurosci

Institute for Cell Biology and Neuroscience, Biologicum, Goethe-University, Frankfurt am Main, Germany. Electronic address:

Published: March 2014

AI Article Synopsis

  • Researchers have developed a method to isolate the presynaptic active zone from individual mouse brains to better understand neurotransmitter release mechanisms.
  • Using an antibody against the protein SV2, they were able to purify synaptic vesicles attached to the presynaptic membrane.
  • Their analysis identified 485 proteins that highlight the active zone's role not just in neurotransmitter release but also in various changes during nerve activity, paving the way for future studies on neurological diseases in mutant mice.

Article Abstract

Neurotransmitter release as well as the structural and functional dynamics of the presynaptic active zone is controlled by proteinaceous components. Here we describe for the first time an experimental approach for the isolation of the presynaptic active zone from individual mouse brains, a prerequisite for understanding the functional inventory of the presynaptic protein network and for the later analysis of changes occurring in mutant mice. Using a monoclonal antibody against the ubiquitous synaptic vesicle protein SV2 we immunopurified synaptic vesicles docked to the presynaptic plasma membrane. Enrichment studies by means of Western blot analysis and mass spectrometry identified 485 proteins belonging to an impressive variety of functional categories. Our data suggest that presynaptic active zones represent focal hot spots that are not only involved in the regulation of neurotransmitter release but also in multiple structural and functional alterations the adult nerve terminal undergoes during neural activity in adult CNS. They furthermore open new avenues for characterizing alterations in the active zone proteome of mutant mice and their corresponding controls, including the various mouse models of neurological diseases.

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http://dx.doi.org/10.1016/j.mcn.2014.02.003DOI Listing

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