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通过糖脂组学图谱解析小鼠大脑空间多样性。

Deciphering mouse brain spatial diversity via glyco-lipidomic mapping.

机构信息

Proteomics Center of Excellence, Chemistry of Life Processes Institute, Northwestern University, Evanston, IL, USA.

Graduate School of Analytical Science & Technology, Chungnam National University, 34134, Daejeon, South Korea.

出版信息

Nat Commun. 2024 Oct 7;15(1):8689. doi: 10.1038/s41467-024-53032-8.

Abstract

Gangliosides in the brain play a crucial role in modulating the integrity of vertebrate central nervous system in a region-specific manner. However, to date, a comprehensive structural elucidation of complex intact ganglioside isomers has not been achieved, resulting in the elusiveness into related molecular mechanism. Here, we present a glycolipidomic approach for isomer-specific and brain region-specific profiling of the mouse brain. Considerable region-specificity and commonality in specific group of regions are highlighted. Notably, we observe a similarity in the abundance of major isomers, GD1a and GD1b, within certain regions, which provides significant biological implications with interpretation through the lens of a theoretical retrosynthetic state-transition network. Furthermore, A glycocentric-omics approaches using gangliosides and N-glycans reveal a remarkable convergence in spatial dynamics, providing valuable insight into molecular interaction network. Collectively, this study uncovers the spatial dynamics of intact glyco-conjugates in the brain, which are relevant to regional function and accelerates the discovery of potential therapeutic targets for brain diseases.

摘要

脑内神经节苷脂以区域特异性方式在调节脊椎动物中枢神经系统的完整性方面发挥着至关重要的作用。然而,迄今为止,尚未实现对复杂完整神经节苷脂异构体的全面结构阐明,这导致相关分子机制难以捉摸。在这里,我们提出了一种用于对小鼠大脑进行异构体特异性和脑区特异性分析的糖脂组学方法。突出显示了相当大的区域特异性和特定区域组的共性。值得注意的是,我们观察到某些区域内 GD1a 和 GD1b 等主要异构体的丰度相似,这通过理论回溯合成状态转换网络的视角提供了重要的生物学意义。此外,使用神经节苷脂和 N-聚糖的糖中心组学方法揭示了空间动态的显著收敛,为分子相互作用网络提供了有价值的见解。总的来说,这项研究揭示了脑内完整糖缀合物的空间动态,这与区域功能有关,并加速了针对脑部疾病的潜在治疗靶点的发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c35/11458762/ca466d999605/41467_2024_53032_Fig1_HTML.jpg

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