Matsubayashi Junpei, Takano Tetsuya
Division of Molecular Systems for Brain Function, Medical Institute of Bioregulation, Kyushu University Institute for Advanced Study, Fukuoka, Japan.
PRESTO, Japan Science and Technology Agency, Saitama, Japan.
Front Cell Neurosci. 2025 Jul 23;19:1638627. doi: 10.3389/fncel.2025.1638627. eCollection 2025.
Synapses are fundamental units of neurotransmission and play a central role in the formation and function of neural circuits. These dynamic structures exhibit morphological and functional plasticity in response to experience and activity, supporting higher brain functions such as learning, memory, and emotion. Their molecular composition includes diverse membrane-associated and cytoskeletal proteins that mediate intercellular signaling, regulate synaptic plasticity, and maintain structural stability. Disruptions in these protein networks, often referred to as synaptopathies, are closely linked to psychiatric and neurological disorders. Such disruptions commonly manifest as region-specific changes in synapse number, morphology, or signaling efficacy. Although a large number of synaptic proteins have been identified through conventional proteomic approaches, our understanding of synaptic specificity and plasticity remains limited. This is primarily due to insufficient spatial resolution, lack of cell-type specificity, and challenges in applying these methods to intact neural circuits . Recent advances in proximity labeling techniques such as BioID and APEX can spatial proteomics limiting cell compartments and cell-type. BioID also enables proteomic analysis within synaptic compartments under both physiological and pathological conditions . These technologies allow unbiased, high-resolution profiling of protein networks in specific synapse types, synaptic clefts, and glial-neuronal interfaces, thereby providing new insights into the molecular basis of synaptic diversity and function. In this short review, we summarize recent developments in synaptic proteomics enabled by proximity labeling. We also discuss how these approaches have advanced our understanding of synapse-specific molecular architecture and their potential to inform the mechanisms of synapse-related brain disorders, as well as the development of targeted diagnostic and therapeutic strategies.
突触是神经传递的基本单位,在神经回路的形成和功能中起着核心作用。这些动态结构会根据经验和活动表现出形态和功能可塑性,支持学习、记忆和情感等高级脑功能。它们的分子组成包括多种与膜相关的和细胞骨架蛋白,这些蛋白介导细胞间信号传导、调节突触可塑性并维持结构稳定性。这些蛋白质网络的破坏,通常被称为突触病变,与精神和神经疾病密切相关。这种破坏通常表现为突触数量、形态或信号传导效率的区域特异性变化。尽管通过传统蛋白质组学方法已经鉴定出大量突触蛋白,但我们对突触特异性和可塑性的理解仍然有限。这主要是由于空间分辨率不足、缺乏细胞类型特异性以及将这些方法应用于完整神经回路时面临的挑战。BioID和APEX等邻近标记技术的最新进展可以对细胞区室和细胞类型进行空间蛋白质组学分析。BioID还能够在生理和病理条件下对突触区室内进行蛋白质组学分析。这些技术允许对特定突触类型、突触间隙和神经胶质-神经元界面中的蛋白质网络进行无偏倚的高分辨率分析,从而为突触多样性和功能的分子基础提供新的见解。在这篇简短的综述中,我们总结了邻近标记技术在突触蛋白质组学方面的最新进展。我们还讨论了这些方法如何推进了我们对突触特异性分子结构的理解,以及它们为了解与突触相关的脑部疾病机制、开发靶向诊断和治疗策略提供信息的潜力。