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Fluorescent Protein-Based Autophagy Biosensors

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 biochemi...

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Detalles Bibliográficos
Autores principales: Kim, Heejung, Seong, Jihye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8199620/
https://www.ncbi.nlm.nih.gov/pubmed/34199451
http://dx.doi.org/10.3390/ma14113019
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author Kim, Heejung
Seong, Jihye
author_facet Kim, Heejung
Seong, Jihye
author_sort Kim, Heejung
collection PubMed
description 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.
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spelling pubmed-81996202021-06-14 Fluorescent Protein-Based Autophagy Biosensors Kim, Heejung Seong, Jihye Materials (Basel) Review 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. MDPI 2021-06-02 /pmc/articles/PMC8199620/ /pubmed/34199451 http://dx.doi.org/10.3390/ma14113019 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Kim, Heejung
Seong, Jihye
Fluorescent Protein-Based Autophagy Biosensors
title Fluorescent Protein-Based Autophagy Biosensors
title_full Fluorescent Protein-Based Autophagy Biosensors
title_fullStr Fluorescent Protein-Based Autophagy Biosensors
title_full_unstemmed Fluorescent Protein-Based Autophagy Biosensors
title_short Fluorescent Protein-Based Autophagy Biosensors
title_sort fluorescent protein-based autophagy biosensors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8199620/
https://www.ncbi.nlm.nih.gov/pubmed/34199451
http://dx.doi.org/10.3390/ma14113019
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