Gundelfinger Eckart D, Reissner Carsten, Garner Craig C
Department Neurochemistry and Molecular Biology, Leibniz Institute for NeurobiologyMagdeburg, Germany; Center for Behavioral Brain SciencesMagdeburg, Germany; Medical Faculty, Otto von Guericke UniversityMagdeburg, Germany; German Center for Neurodegenerative Diseases (DZNE) Site MagdeburgMagdeburg, Germany.
Institute of Anatomy and Molecular Neurobiology, Westfälische Wilhelms University Münster, Germany.
Front Synaptic Neurosci. 2016 Jan 12;7:19. doi: 10.3389/fnsyn.2015.00019. eCollection 2015.
Bassoon and Piccolo are two very large scaffolding proteins of the cytomatrix assembled at the active zone (CAZ) where neurotransmitter is released. They share regions of high sequence similarity distributed along their entire length and seem to share both overlapping and distinct functions in organizing the CAZ. Here, we survey our present knowledge on protein-protein interactions and recent progress in understanding of molecular functions of these two giant proteins. These include roles in the assembly of active zones (AZ), the localization of voltage-gated Ca(2+) channels (VGCCs) in the vicinity of release sites, synaptic vesicle (SV) priming and in the case of Piccolo, a role in the dynamic assembly of the actin cytoskeleton. Piccolo and Bassoon are also important for the maintenance of presynaptic structure and function, as well as for the assembly of CAZ specializations such as synaptic ribbons. Recent findings suggest that they are also involved in the regulation activity-dependent communication between presynaptic boutons and the neuronal nucleus. Together these observations suggest that Bassoon and Piccolo use their modular structure to organize super-molecular complexes essential for various aspects of presynaptic function.
巴松管蛋白和短笛蛋白是位于活性区(CAZ)的细胞基质中两个非常大的支架蛋白,神经递质在此释放。它们在整个长度上都有高度序列相似性的区域,并且在组织CAZ方面似乎具有重叠和不同的功能。在这里,我们综述了目前关于这两种巨型蛋白的蛋白质-蛋白质相互作用的知识以及在其分子功能理解方面的最新进展。这些功能包括在活性区(AZ)组装中的作用、电压门控钙通道(VGCCs)在释放位点附近的定位、突触小泡(SV)的启动,以及对于短笛蛋白而言,在肌动蛋白细胞骨架动态组装中的作用。巴松管蛋白和短笛蛋白对于突触前结构和功能的维持,以及对于CAZ特化结构如突触带的组装也很重要。最近的研究结果表明,它们还参与调节突触前终扣与神经元细胞核之间的活动依赖性通讯。这些观察结果共同表明,巴松管蛋白和短笛蛋白利用其模块化结构来组织突触前功能各个方面所必需的超分子复合物。