Murthy Meesala Krishna, Khandayataray Pratima, Samal Dibyaranjan, Pattanayak Rojalin, Mohanty Chandra Sekhar
Department of Allied Health Sciences, Chitkara School of Health Sciences, Chitkara University, Rajpura, Punjab, India.
Department of Biotechnology, Academy of Management and Information Technology, Utkal University, Bhubaneswar, Odisha, India.
Methods Mol Biol. 2025;2879:1-22. doi: 10.1007/7651_2023_508.
Autophagy is a vital cellular process responsible for breaking down faulty cellular components and organelles, ultimately routed through lysosomes for degradation. This intricate mechanism involves the translocation of LC3, a cytoplasmic protein, onto the autophagosome membranes. As a result, it becomes feasible to discern cells engaged in autophagy by employing fluorescent markers designed for LC3 or other indicative autophagy markers. Although a variety of techniques such as immunofluorescence and western blotting serve as indispensable tools for assessing autophagy, the definitive confirmation comes from the visualization of autophagosomes using transmission electron microscopy. While numerous protocols for antibody staining can be found in scientific literature and on antibody suppliers' websites, these procedures often demand significant time and financial resources for setup. This chapter endeavors to provide a user-friendly and cost-effective guide for practitioners seeking proficiency in immunofluorescence staining and western blotting techniques.
自噬是一种重要的细胞过程,负责分解有缺陷的细胞成分和细胞器,最终通过溶酶体进行降解。这种复杂的机制涉及一种细胞质蛋白LC3向自噬体膜的转运。因此,通过使用针对LC3或其他指示性自噬标记物设计的荧光标记物来识别参与自噬的细胞成为可能。尽管诸如免疫荧光和蛋白质印迹等多种技术是评估自噬不可或缺的工具,但最终的确证来自使用透射电子显微镜对自噬体的可视化观察。虽然在科学文献和抗体供应商的网站上可以找到许多抗体染色方案,但这些程序通常需要大量的时间和资金来进行设置。本章旨在为寻求熟练掌握免疫荧光染色和蛋白质印迹技术的从业人员提供一份用户友好且经济高效的指南。