Publication | Open Access
Distribution of Postsynaptic Density (PSD)-95 and Ca<sup>2+</sup>/Calmodulin-Dependent Protein Kinase II at the PSD
202
Citations
39
References
2003
Year
Protein SecretionSynaptic TransmissionMolecular BiologyNeurotransmissionSynaptic SignalingCellular PhysiologySocial SciencesPsds LabelCell SignalingBiophysicsProtein FunctionMolecular NeuroscienceMolecular PhysiologyProtein TransportCell BiologyStructural BiologyProtein PhosphorylationSynaptic PlasticitySignal TransductionNeurophysiologyPhysiologyCleft SidesNeuroscienceMolecular NeurobiologyIntracellular TraffickingCellular BiochemistryCellular StructureMedicineCleft SidePostsynaptic Density
Postsynaptic densities (PSDs) contain proteins that regulate synaptic transmission. We determined the positions of calcium/calmodulin-dependent protein kinase II (CaMKII) and PSD-95 within the three-dimensional structure of isolated PSDs using immunogold labeling, rotary shadowing, and electron microscopic tomography. The results show that all PSDs contain a central mesh immediately underlying the postsynaptic membrane. Label for PSD-95 is found on both the cytoplasmic and cleft sides of this mesh, averaging 12 nm from the cleft side. All PSDs label for PSD-95. The properties of CaMKII labeling are quite different. Label is virtually absent on the cleft sides of PSDs, but can be heavy on the cytoplasmic side at a mean distance of 25 nm from the cleft. In tomograms, CaMKII holoenzymes can be visualized directly, appearing as labeled, tower-like structures reflecting the 20 nm diameter of the holoenzyme. These towers protrude from the cytoplasmic side of the central mesh. There appears to be a local organization of CaMKII, as judged by fact that the nearest-neighbor distances are nearly invariant over a wide range of labeling density for CaMKII. The average density of CaMKII holoenzymes is highly variable, ranging from zero to values approaching a tightly packed state. This variability is significantly higher than that for PSD-95 and is consistent with an information storage role for CaMKII.
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