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Interactions of synapsin I with small synaptic vesicles: distinct sites in synapsin I bind to vesicle phospholipids and vesicle proteins

机译:突触素I与小的突触囊泡的相互作用:突触素I中的不同位点结合到囊泡磷脂和囊泡蛋白

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摘要

Synapsin I is a major neuron-specific phosphoprotein that is specifically localized to the cytoplasmic surface of small synaptic vesicles. In the present study, the binding of synapsin I to small synaptic vesicles was characterized in detail. The binding of synapsin I was preserved when synaptic vesicles were solubilized and reconstituted in phosphatidylcholine. After separation of the protein and lipid components of synaptic vesicles under nondenaturing conditions, synapsin I bound to both components. The use of hydrophobic labeling procedures allowed the assessment of interactions between phospholipids and synapsin I in intact synaptic vesicles. Hydrophobic photolabeling followed by cysteine-specific cleavage of synapsin I demonstrated that the head domain of synapsin I penetrates into the hydrophobic core of the bilayer. The purified NH2-terminal fragment, derived from the head domain by cysteine-specific cleavage, bound to synaptic vesicles with high affinity confirming the results obtained from hydrophobic photolabeling. Synapsin I binding to synaptic vesicles could be inhibited by the entire molecule or by the combined presence of the NH2-terminal and tail fragments, but not by an excess of either NH2-terminal or tail fragment alone. The purified tail fragment bound with relatively high affinity to synaptic vesicles, though it did not significantly interact with phospholipids. Binding of the tail fragment was competed by holosynapsin I; was greatly decreased by phosphorylation; and was abolished by high ionic strength conditions or protease treatment of synaptic vesicles. The data suggest the existence of two sites of interaction between synapsin I and small synaptic vesicles: binding of the head domain to vesicle phospholipids and of the tail domain to a protein component of the vesicle membrane. The latter interaction is apparently responsible for the salt and phosphorylation dependency of synapsin I binding to small synaptic vesicles.
机译:突触素I是主要的神经元特异性磷蛋白,特异性定位在小突触小泡的胞质表面。在本研究中,详细描述了突触素I与小突触小泡的结合。当突触囊泡溶解并在磷脂酰胆碱中重构时,突触素I的结合得以保留。在非变性条件下分离突触小泡的蛋白质和脂质成分后,突触素I结合到这两种成分。疏水性标记程序的使用允许完整的突触囊泡中的磷脂和突触素I之间的相互作用的评估。疏水性光标记,然后半胱氨酸特异性切割突触素I,表明突触素I的头部结构域渗透到双层的疏水核中。通过半胱氨酸特异性切割从头部结构域衍生的纯化的NH2末端片段以高亲和力结合到突触小泡,从而证实了从疏水性光标记获得的结果。突触素I与突触小泡的结合可被整个分子或NH 2末端和尾部片段的结合存在抑制,但不被单独的NH 2末端或尾部片段的过量抑制。纯化的尾巴片段与突触小泡的结合相对较高,尽管它与磷脂没有明显的相互作用。尾片段的结合被holosynapsin I竞争。被磷酸化大大降低;并被高离子强度条件或突触小泡的蛋白酶处理所取消。数据表明突触素I和小的突触囊泡之间存在两个相互作用的位点:头部域与囊泡磷脂结合,而尾部域与囊泡膜蛋白成分结合。后者的相互作用显然是突触素I与小突触小泡结合的盐和磷酸化依赖性的原因。

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