Synaptotagmin VIII play pivotal roles in its functional engagement in the complex process of synaptic vesicle fusion. Calcium chloride is a prime activator of Synaptotagmin VIII, where the influx of calcium ions (Ca2+) directly binds to the C2 domains of the protein, an action that is fundamental for the mediation of vesicle fusion at the presynaptic terminal. This binding prompts a conformational change in Synaptotagmin VIII, which, in conjunction with SNARE proteins, leads to the fusion of synaptic vesicles with the plasma membrane and subsequent neurotransmitter release. Similarly, phosphatidylinositol 4,5-bisphosphate (PIP2), a phospholipid located in the plasma membrane, also engages with Synaptotagmin VIII. The interaction between PIP2 and Synaptotagmin VIII facilitates the protein's membrane association, thereby enhancing its role in neurotransmitter release.
Fatty acids such as eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), arachidonic acid, oleic acid, linoleic acid, and alpha-linolenic acid, contribute to the regulation of synaptic membrane properties. These fatty acids can be integrated into the membrane, altering its fluidity and curvature, which in turn can support the vesicle fusion mediated by Synaptotagmin VIII. The proper integration and balance of these fatty acids are vital for maintaining the physical state of the membrane, thus optimizing the conditions for Synaptotagmin VIII to facilitate vesicle docking and fusion. Additionally, sphingosine and ceramide, components of the lipid signaling pathway, can modulate the structural integrity of the membrane. They play a role in the organization of lipid microdomains which may enable more efficient binding and function of Synaptotagmin VIII in the exocytotic process. Cholesterol and sphingomyelin, by influencing the membrane's fluidity and domain formation, can also contribute to the optimal environment for Synaptotagmin VIII activation and function. Cholesterol, in particular, by affecting the biophysical properties of the synaptic vesicle membrane, can provide a conducive platform for Synaptotagmin VIII to carry out its critical role in neurotransmission.
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