Abstract
A fraction enriched in synaptic complexes has been isolated from rat brain. The major structural elements of synaptic complexes after isolation are a sector of pre- and postsynaptic plasma membranes joined together by a synaptic cleft and a postsynaptic density (PSD) located on the inner surface of the postsynaptic membrane. On its outer surface, the postsynaptic membrane has a series of projections which extend about halfway into the cleft and which occur along the entire length of the PSD. Proteolytic enzymes at high concentrations remove the PSD and open the synaptic cleft; at low concentrations the PSD is selectively destroyed. By contrast, the structural integrity of the PSD is resistant to treatment with NaCl, EGTA, and low concentrations of urea. Pre- and postsynaptic membranes also remain joined by the synaptic cleft after NaCl, EGTA, or mild urea treatment. High concentrations of urea cause the partial dissociation of the PSD. We conclude that polypeptides are probably one of the major components of the PSD and that the structural integrity of the PSD depends on polypeptides because disruption of the covalent or hydrophobic bonding of these polypeptides leads to a progressive loss of PSD structure.
MeSH Terms
Acetates/pharmacology
Animals
Brain/cytology,drug effects
Brain Chemistry
Cell Fractionation
Centrifugation, Density Gradient
Chymotrypsin/pharmacology
Glycols/pharmacology
Male
Microscopy, Electron
Nerve Tissue Proteins/analysis
Rats
Sodium Chloride/pharmacology
Surface-Active Agents
Synaptic Membranes/analysis,drug effects
Trypsin/pharmacology
Urea/pharmacology
Chemicals
Acetates
Glycols
Nerve Tissue Proteins
Surface-Active Agents
Sodium Chloride
Urea
Chymotrypsin
Trypsin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Cotman C W
Taylor D
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20 references, click to expand
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