University of Wisconsin Medical School, Department of Neuroscience, Madison, Wisconsin.
University of Wisconsin Medical School, Department of Neuroscience, Madison, Wisconsin.
Biophys J. 2020 Jul 7;119(1):219-231. doi: 10.1016/j.bpj.2020.06.001. Epub 2020 Jun 8.
Amperometry recording reveals the exocytosis of catecholamine from individual vesicles as a sequential process, typically beginning slowly with a prespike foot, accelerating sharply to initiate a spike, reaching a peak, and then decaying. This complex sequence reflects the interplay between diffusion, flux through a fusion pore, and possibly dissociation from a vesicle's dense core. In an effort to evaluate the impacts of these factors, a model was developed that combines diffusion with flux through a static pore. This model accurately recapitulated the rapid phase of a spike but generated relations between spike shape parameters that differed from the relations observed experimentally. To explore the possible role of fusion pore dynamics, a transformation of amperometry current was introduced that yields fusion pore permeability divided by vesicle volume (g/V). Applying this transform to individual fusion events yielded a highly characteristic time course. g/V initially tracks the current, increasing ∼15-fold from the prespike foot to the spike peak. After the peak, g/V unexpectedly declines and settles into a plateau that indicates the presence of a stable postspike pore. g/V of the postspike pore varies greatly between events and has an average that is ∼3.5-fold below the peak value and ∼4.5-fold above the prespike value. The postspike pore persists and is stable for tens of milliseconds, as long as catecholamine flux can be detected. Applying the g/V transform to rare events with two peaks revealed a stepwise increase in g/V during the second peak. The g/V transform offers an interpretation of amperometric current in terms of fusion pore dynamics and provides a, to our knowledge, new frameworkfor analyzing the actions of proteins that alter spike shape. The stable postspike pore follows from predictions of lipid bilayer elasticity and offers an explanation for previous reports of prolonged hormone retention within fusing vesicles.
电流钳位记录揭示了儿茶酚胺从单个囊泡中的胞吐作用是一个顺序过程,通常以一个预脉冲足开始,缓慢加速到起始一个尖峰,达到峰值,然后衰减。这个复杂的序列反映了扩散、通过融合孔的通量和可能与囊泡致密核心的解离之间的相互作用。为了评估这些因素的影响,开发了一个将扩散与通过静态孔的通量相结合的模型。该模型准确地再现了尖峰的快速阶段,但产生的尖峰形状参数之间的关系与实验观察到的关系不同。为了探索融合孔动力学的可能作用,引入了一种对电流的转换,该转换产生融合孔渗透率与囊泡体积的比值 (g/V)。将该转换应用于单个融合事件,得到了一个非常特征性的时程。g/V 最初与电流跟踪,从预脉冲足到尖峰峰值增加约 15 倍。峰值后,g/V 出人意料地下降并稳定在一个平台上,表明存在一个稳定的尖峰后孔。尖峰后孔的 g/V 在事件之间变化很大,平均值比峰值低约 3.5 倍,比预脉冲值高约 4.5 倍。只要儿茶酚胺通量可以检测到,尖峰后孔就会持续存在并保持稳定数十毫秒。将 g/V 转换应用于具有两个峰值的罕见事件揭示了 g/V 在第二个峰值期间的逐步增加。g/V 转换提供了一种基于融合孔动力学的电流解释,并为分析改变尖峰形状的蛋白质的作用提供了一个,据我们所知,新的框架。稳定的尖峰后孔来自于脂质双层弹性的预测,并为以前关于融合囊泡内激素保留时间延长的报告提供了解释。