Bennett M K, Scheller R H
Howard Hughes Medical Institute, Beckman Center, Department of Molecular and Cellular Physiology, Stanford University, CA 94305.
Proc Natl Acad Sci U S A. 1993 Apr 1;90(7):2559-63. doi: 10.1073/pnas.90.7.2559.
A variety of approaches have been utilized to identify and characterize the molecules that mediate vesicular trafficking along the secretory pathway. Two approaches that have been particularly fruitful include the genetic dissection of the yeast secretory pathway and the biochemical characterization of proteins involved in the synaptic vesicle membrane trafficking in the mammalian nerve terminal. The recent convergence of these approaches suggests that common mechanisms may underlie a wide variety of vesicle-mediated transport steps. We discuss the results that support this possibility and propose a model for synaptic vesicle docking and fusion that incorporates evolutionarily conserved elements that may be part of a constitutive fusion machinery and specialized elements that may mediate regulatory events that are specific to the process of neurotransmitter release.
人们已经采用了多种方法来识别和表征介导沿分泌途径进行囊泡运输的分子。两种特别有成效的方法包括对酵母分泌途径的遗传学剖析以及对参与哺乳动物神经末梢突触囊泡膜运输的蛋白质进行生化表征。最近这些方法的融合表明,多种囊泡介导的运输步骤可能存在共同机制。我们讨论了支持这种可能性的结果,并提出了一个突触囊泡对接和融合的模型,该模型纳入了可能是组成型融合机制一部分的进化保守元件以及可能介导特定于神经递质释放过程的调节事件的特殊元件。