Cotman C W, Taylor D
J Cell Biol. 1972 Dec;55(3):696-711. doi: 10.1083/jcb.55.3.696.
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.
已从大鼠脑中分离出富含突触复合体的部分。分离后突触复合体的主要结构成分是由突触间隙连接在一起的突触前和突触后质膜的一个部分,以及位于突触后膜内表面的突触后致密区(PSD)。在其外表面,突触后膜有一系列突起,这些突起延伸到间隙的大约一半处,并沿着PSD的全长出现。高浓度的蛋白水解酶会去除PSD并打开突触间隙;低浓度时,PSD会被选择性破坏。相比之下,PSD的结构完整性对NaCl、EGTA和低浓度尿素的处理具有抗性。在NaCl、EGTA或温和的尿素处理后,突触前和突触后膜也仍由突触间隙连接。高浓度的尿素会导致PSD部分解离。我们得出结论,多肽可能是PSD的主要成分之一,并且PSD的结构完整性取决于多肽,因为这些多肽的共价或疏水键的破坏会导致PSD结构逐渐丧失。