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光学显微镜监测自噬。

Monitoring Autophagy by Optical Microscopy.

机构信息

Institute of Pharmacology and Toxicology, NHC and CAMS Key Laboratory of Medical Neurobiology, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.

Key Laboratory of Neuropharmacology and Translational Medicine of Zhejiang Province, Zhejiang Chinese Medical University, Hangzhou, China.

出版信息

Adv Exp Med Biol. 2021;1208:117-130. doi: 10.1007/978-981-16-2830-6_8.

Abstract

Thanks to the advances in optical microscope technology and our knowledge of autophagic biomarkers, single-molecule events of autophagy are now accessible to human eyes. Different proteins are involved hierarchically in the biogenesis and maturation of autophagosomes. Detecting these autophagy-related proteins either by immunostaining or fluorescent protein labelling makes the dynamic autophagic process visible. However, low antibody specificity and weak endogenous expression of autophagy-related proteins in certain tissues limit the applicability of immunostaining in autophagy detection. To cope with this, live-cell imaging combined with various fluorescent probes has been developed and employed in monitoring autophagy. As the most widely used autophagic biomarker, LC3 can be used to visualize autophagosomes, and fluorescent probes targeting LC3, i.e., RFP/mCherry-GFP-LC3, and GFP-LC3-RFP-LC3ΔG, can examine autophagy flux dynamically and quantitatively. In addition, the application of novel fluorophores such as Keima helps to detect the temporal and spatial characteristics of autophagy. Furthermore, selective autophagy can be clarified by labelling corresponding substrates and autophagosomes or lysosomes simultaneously. With the help of two-photon microscopy, the process of autophagy in live animals has been uncovered. Here, we summarize the methods for observing autophagy by optical microscopy and the selection of fluorescent markers.

摘要

得益于光学显微镜技术的进步和我们对自噬生物标志物的了解,人类现在可以观察到自噬的单分子事件。不同的蛋白质在自噬体的生物发生和成熟过程中按层次参与。通过免疫染色或荧光蛋白标记检测这些自噬相关蛋白,使动态自噬过程可见。然而,免疫染色在自噬检测中的应用受到抗体特异性低和某些组织中自噬相关蛋白内源性表达弱的限制。为了解决这个问题,已经开发并采用活细胞成像结合各种荧光探针来监测自噬。作为最广泛使用的自噬生物标志物,LC3 可用于可视化自噬体,并且靶向 LC3 的荧光探针,即 RFP/mCherry-GFP-LC3 和 GFP-LC3-RFP-LC3ΔG,可以动态和定量地检查自噬流。此外,新型荧光团如 Keima 的应用有助于检测自噬的时空特征。此外,通过同时标记相应的底物和自噬体或溶酶体,可以阐明选择性自噬。借助双光子显微镜,揭示了活体内动物自噬的过程。在这里,我们总结了通过光学显微镜观察自噬的方法和荧光标记的选择。

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