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无标记二次谐波成像微管的分子机制研究。

Molecular understanding of label-free second harmonic imaging of microtubules.

机构信息

Laboratory for Enteric NeuroScience (LENS), TARGID, Department of Chronic Diseases Metabolism and Ageing, KU Leuven, Leuven, Belgium.

Department of Pathology, GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.

出版信息

Nat Commun. 2019 Aug 6;10(1):3530. doi: 10.1038/s41467-019-11463-8.

Abstract

Microtubules are a vital component of the cell's cytoskeleton and their organization is crucial for healthy cell functioning. The use of label-free SH imaging of microtubules remains limited, as sensitive detection is required and the true molecular origin and main determinants required to generate SH from microtubules are not fully understood. Using advanced correlative imaging techniques, we identified the determinants of the microtubule-dependent SH signal. Microtubule polarity, number and organization determine SH signal intensity in biological samples. At the molecular level, we show that the GTP-bound tubulin dimer conformation is fundamental for microtubules to generate detectable SH signals. We show that SH imaging can be used to study the effects of microtubule-targeting drugs and proteins and to detect changes in tubulin conformations during neuronal maturation. Our data provide a means to interpret and use SH imaging to monitor changes in the microtubule network in a label-free manner.

摘要

微管是细胞骨架的重要组成部分,其组织对于细胞的正常功能至关重要。由于需要敏感的检测,并且对微管产生 SH 的真正分子起源和主要决定因素还不完全了解,因此无标记 SH 成像在微管中的应用仍然有限。本研究使用先进的相关成像技术,确定了微管依赖性 SH 信号的决定因素。微管的极性、数量和组织决定了生物样本中 SH 信号的强度。在分子水平上,我们表明,结合 GTP 的微管二聚体构象是微管产生可检测 SH 信号的基础。我们表明,SH 成像可用于研究微管靶向药物和蛋白质的作用,并检测神经元成熟过程中微管构象的变化。我们的数据提供了一种解释和使用 SH 成像的方法,以无标记的方式监测微管网络的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6de/6684603/d8f1e96075c5/41467_2019_11463_Fig1_HTML.jpg

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