Fluorescent Protein-Based Autophagy Biosensors

被引:6
|
作者
Kim, Heejung [1 ,2 ]
Seong, Jihye [1 ,2 ]
机构
[1] Korea Inst Sci & Technol KIST, Brain Sci Inst, Seoul 02792, South Korea
[2] Kyung Hee Univ, Dept Converging Sci & Technol, Seoul 02453, South Korea
关键词
autophagy; fluorescence imaging; fluorescent protein; biosensors; neurodegenerative diseases; CHAPERONE-MEDIATED AUTOPHAGY; ALPHA-SYNUCLEIN; PARKINSONS-DISEASE; MONOMERIC RED; PH-BIOSENSOR; DEGRADATION; LC3; CYAN; FLUX; MACROAUTOPHAGY;
D O I
10.3390/ma14113019
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Autophagy is an essential cellular process of self-degradation for dysfunctional or unnecessary cytosolic constituents and organelles. Dysregulation of autophagy is thus involved in various diseases such as neurodegenerative diseases. To investigate the complex process of autophagy, various biochemical, chemical assays, and imaging methods have been developed. Here we introduce various methods to study autophagy, in particular focusing on the review of designs, principles, and limitations of the fluorescent protein (FP)-based autophagy biosensors. Different physicochemical properties of FPs, such as pH-sensitivity, stability, brightness, spectral profile, and fluorescence resonance energy transfer (FRET), are considered to design autophagy biosensors. These FP-based biosensors allow for sensitive detection and real-time monitoring of autophagy progression in live cells with high spatiotemporal resolution. We also discuss future directions utilizing an optobiochemical strategy to investigate the in-depth mechanisms of autophagy. These cutting-edge technologies will further help us to develop the treatment strategies of autophagy-related diseases.
引用
收藏
页数:20
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