eSylites: Synthetic Probes for Visualization and Topographic Mapping of Single Excitatory Synapses

IF 15.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of the American Chemical Society Pub Date : 2025-03-20 DOI:10.1021/jacs.5c00772
Christiane Huhn, Sheng-Yang Ho, Clemens Schulte, Vladimir Khayenko, Katherina Hemmen, Thomas-Otavio Peulen, Anna-Lena Wiessler, Sebastian Bothe, Aritra Bej, Ivan Talucci, Lars Schönemann, Christian Werner, Hermann Schindelin, Kristian Strømgaard, Carmen Villmann, Katrin G. Heinze, Martin Hruska, Johannes W. Hell, Hans M. Maric
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Abstract

The spatiotemporal organization of the postsynaptic density (PSD) is a fundamental determinant of synaptic transmission, information processing, and storage in the brain. The major bottleneck that prevents the direct and precise representation of the nanometer-scaled organization of excitatory glutamatergic synapses is the size of antibodies, nanobodies, and the genetically encoded fluorescent tags. Here, we introduce small, high affinity synthetic probes for simplified, high contrast visualization of excitatory synapses without the limitations of larger biomolecules. In vitro binding quantification together with microscopy-based evaluation identified eSylites, a series of fluorescent bivalent peptides comprising a dye, linker, and sequence composition that show remarkable cellular target selectivity. Applied on primary neurons or brain slices at nanomolar concentrations, eSylites specifically report PSD-95, the key orchestrator of glutamate receptor nanodomains juxtaposed to the presynaptic glutamate release sites that mediate fast synaptic transmission. The eSylite design minimizes a spatial dye offset and thereby enables visualization of PSD-95 with improved localization precision and further time-resolved discrimination. In particular, we find that individual dendritic spines can contain separate nanodomains enriched for either PSD-95 or its closest homologues, PSD-93 or SAP102. Collectively, these data establish eSylites as a broadly applicable tool for simplified excitatory synapse visualization, as well as a high-end microscopy compatible probe for resolving the PSD organization with unprecedented resolution.

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eSylites:用于单个兴奋性突触可视化和地形测绘的合成探针
突触后密度(PSD)的时空组织是大脑突触传递、信息处理和存储的基本决定因素。阻碍直接和精确表征兴奋性谷氨酸突触纳米级组织的主要瓶颈是抗体、纳米体和遗传编码荧光标记的大小。在这里,我们引入了小的,高亲和力的合成探针,用于简化,高对比度的兴奋性突触可视化,而不受较大生物分子的限制。体外结合定量和基于显微镜的评价鉴定了eSylites,这是一系列由染料、连接剂和序列组成的荧光二价肽,具有显著的细胞靶标选择性。eSylites特别报道了PSD-95,它是谷氨酸受体纳米结构域的关键协调者,与介导快速突触传递的突触前谷氨酸释放位点并置于一起。eSylite设计最大限度地减少了空间染料偏移,从而使PSD-95的可视化具有更高的定位精度和进一步的时间分辨能力。特别是,我们发现单个树突棘可以包含单独的纳米结构域,这些纳米结构域富含PSD-95或其最接近的同源物PSD-93或SAP102。总的来说,这些数据使eSylites成为一种广泛适用的简化兴奋性突触可视化工具,以及一种高端显微镜兼容探针,以前所未有的分辨率解决PSD组织。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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