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通过冷冻电子断层扫描对神经元分子组织的深入了解。

Insights into the molecular organization of the neuron by cryo-electron tomography.

作者信息

Fernández-Busnadiego Rubén, Schrod Nikolas, Kochovski Zdravko, Asano Shoh, Vanhecke Dimitri, Baumeister Wolfgang, Lucic Vladan

机构信息

Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152 Martinsried, Germany.

出版信息

J Electron Microsc (Tokyo). 2011;60 Suppl 1:S137-48. doi: 10.1093/jmicro/dfr018.

Abstract

Despite great progress in the identification and characterization of the key molecular players in neuronal function, remarkably little is known about their supramolecular organization. Cryo-electron tomography (cryo-ET), providing three-dimensional views of the molecular components of the cell in their native, fully hydrated environment, is uniquely positioned to elucidate the native architecture of the molecular machinery of the neuron. In our laboratory, we employ cryo-ET to study neuronal morphology in a variety of experimental systems and develop methods to extract quantitative and functional information from tomographic data. This approach has allowed us to shed light onto the intricate organization of the molecules of the synaptic cleft and the presynaptic cytomatrix, providing evidence for their functional roles. Also, cryo-ET of cultured neurons is beginning to open new perspectives on neuronal ultrastructure and the architecture of synaptic complexes in situ. Here, we will review these findings and discuss future directions towards the elucidation of the molecular landscape of the neuron.

摘要

尽管在识别和表征神经元功能中的关键分子参与者方面取得了巨大进展,但对于它们的超分子组织却知之甚少。冷冻电子断层扫描(cryo-ET)能够在细胞分子成分的天然、完全水合环境中提供三维视图,在阐明神经元分子机制的天然结构方面具有独特的优势。在我们实验室中,我们利用cryo-ET研究各种实验系统中的神经元形态,并开发从断层扫描数据中提取定量和功能信息的方法。这种方法使我们能够深入了解突触间隙和突触前细胞基质分子的复杂组织,为它们的功能作用提供了证据。此外,培养神经元的cryo-ET开始为原位神经元超微结构和突触复合体的结构开辟新的视角。在这里,我们将回顾这些发现,并讨论阐明神经元分子景观的未来方向。

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