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Specific Interaction of Postsynaptic Densities With Membrane Rafts Isolated From Synaptic Plasma Membranes

机译:突触后密度与隔离从突触血浆膜的膜筏的特定相互作用。

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Postsynaptic membrane rafts are believed to play important roles in synaptic signaling, plasticity, and maintenance. We recently demonstrated the presence, at the electron microscopic level, of complexes consisting of membrane rafts and postsynaptic densities (PSDs) in detergent-resistant membranes (DRMs) prepared from synaptic plasma membranes (SPMs) (Suzuki et al., 2011, J Neurochem, 119, 64-11). To further explore these complexes, here we investigated the nature of the binding between purified SPM-DRMs and PSDs in vitro. In binding experiments, we used SPM-DRMs prepared after treating SPMs with n-octyl-beta-D-glucoside, because at concentrations of 1.0% or higher it completely separates SPM-DRMs and PSDs, providing substantially PSD-free unique SPM-DRMs as well as DRM-free PSDs. PSD binding to PSD-free DRMs was identified by mass spectrometry, Western blotting, and electron microscopy. PSD proteins were not incorporated into SPMs, and significantly less PSD proteins were incorporated into DRMs prepared from liver membranes, providing in vitro evidence that binding of PSDs to DRMs is specific and suggestion of the presence of specific interacting molecules. These specific interactions may have important roles in synaptic development, function, and plasticity in vivo. In addition, the binding system we developed may be a good tool to search for binding molecules and binding mechanisms between PSDs and rafts.
机译:认为突触后膜筏在突触信号传导,可塑性和维持中起重要作用。我们最近在电子显微镜下证明了由突触质膜(SPM)制备的去污剂抗性膜(DRM)中由膜筏和突触后密度(PSD)组成的复合物的存在(Suzuki等人,2011,J Neurochem ,119,64-11)。为了进一步探索这些复合物,我们在这里研究了体外纯化的SPM-DRM和PSD之间结合的性质。在结合实验中,我们使用在用正辛基-β-D-葡萄糖苷处理SPM之后制备的SPM-DRM,因为在1.0%或更高的浓度下,它会完全分离SPM-DRM和PSD,从而提供了基本上不含PSD的独特SPM-DRM以及无DRM的PSD。通过质谱,Western印迹和电子显微镜鉴定了PSD与无PSD DRM的结合。 PSD蛋白未掺入SPM中,而从肝膜制备的DRM中掺入的PSD蛋白却少得多,这提供了PSD与DRM结合具有特异性的体外证据,并暗示存在特定相互作用分子。这些特定的相互作用可能在体内的突触发育,功能和可塑性中具有重要作用。此外,我们开发的结合系统可能是搜索PSD和筏之间的结合分子和结合机制的好工具。

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