Dosemeci Ayse, Tao-Cheng Jung-Hwa
Structural Cell Biology Section, National Institutes of Health, Bethesda, MD, 20892, USA.
NINDS Electron Microscopy Facility National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, 20892, USA.
Mol Brain. 2025 May 30;18(1):47. doi: 10.1186/s13041-025-01217-7.
In the synaptic junction, pre-and post compartments are anchored to each other through trans-synaptic bridges spanning the synaptic cleft. Here we demonstrate that mild mechanical disturbance through sonication dissociates the synaptic cleft, and releases PSDs adjoined to the postsynaptic membrane, but devoid of presynaptic elements. It is the first time, to our knowledge, that dissection of the synaptic cleft has been achieved without the use of chemical/enzymatic treatments. This observation suggests that some of the protein-protein interactions involved in the anchoring of pre- and postsynaptic compartments are relatively weak non-covalent associations. We describe a method for the further fractionation of PSDs with the associated postsynaptic membrane. This PSD preparation provides a valuable tool for studies of postsynaptic membrane components, such as glutamatergic receptors, in an environment closer to their native state.
在突触连接处,突触前和突触后部分通过跨越突触间隙的跨突触桥相互锚定。在此我们证明,通过超声处理进行的轻度机械干扰会使突触间隙分离,并释放与突触后膜相连但不含突触前成分的突触后致密物(PSD)。据我们所知,这是首次在不使用化学/酶处理的情况下实现对突触间隙的分离。这一观察结果表明,参与突触前和突触后部分锚定的一些蛋白质-蛋白质相互作用是相对较弱的非共价结合。我们描述了一种对PSD及其相关突触后膜进行进一步分级分离的方法。这种PSD制剂为在更接近其天然状态的环境中研究突触后膜成分(如谷氨酸能受体)提供了一个有价值的工具。