胞吐
蒙克-18
突触蛋白1
细胞生物学
快照25
囊泡融合
分泌物
脂质双层融合
圈套复合体
小泡
高尔基体
生物
STX1A型
激活剂(遗传学)
分泌泡
细胞外
化学
突触融合蛋白
受体
突触小泡
生物化学
膜
内质网
标识
DOI:10.1016/j.tem.2005.02.002
摘要
Secretory vesicles formed at the trans-Golgi network of neuroendocrine and endocrine cells must undergo several steps, such as translocation, docking and priming, before they are ready to fuse with the plasma membrane and deliver their cargo into the extracellular space. This process is called regulated exocytosis and is controlled by Ca(2+) (using synaptotagmin) and mediated by SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptors) proteins. Recent studies from three leading laboratories reveal novel details about the mechanism by which Ca(2+) and SNAREs regulate this complex process. These findings highlight the roles of both SNAP25 (synaptosome-associated protein of 25kD), one of the SNARE proteins, and CAPS (Ca(2+)-dependent activator protein for secretion), a Ca(2+)-sensor protein, in vesicle priming, depriming and fusion.
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