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Enhanced small green fluorescent proteins as a multisensing platform for biosensor development

Engineered light, oxygen, and voltage (LOV)-based proteins are able to fluoresce without oxygen requirement due to the autocatalytic incorporation of exogenous flavin as a chromophore thus allowing for live cell imaging under hypoxic and anaerobic conditions. They were also discovered to have high s...

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Autores principales: Liang, Guo-Teng, Lai, Cuixin, Yue, Zejun, Zhang, Hanbin, Li, Danyang, Chen, Zhong, Lu, Xingyu, Tao, Liang, Subach, Fedor V., Piatkevich, Kiryl D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618808/
https://www.ncbi.nlm.nih.gov/pubmed/36324888
http://dx.doi.org/10.3389/fbioe.2022.1039317
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author Liang, Guo-Teng
Lai, Cuixin
Yue, Zejun
Zhang, Hanbin
Li, Danyang
Chen, Zhong
Lu, Xingyu
Tao, Liang
Subach, Fedor V.
Piatkevich, Kiryl D.
author_facet Liang, Guo-Teng
Lai, Cuixin
Yue, Zejun
Zhang, Hanbin
Li, Danyang
Chen, Zhong
Lu, Xingyu
Tao, Liang
Subach, Fedor V.
Piatkevich, Kiryl D.
author_sort Liang, Guo-Teng
collection PubMed
description Engineered light, oxygen, and voltage (LOV)-based proteins are able to fluoresce without oxygen requirement due to the autocatalytic incorporation of exogenous flavin as a chromophore thus allowing for live cell imaging under hypoxic and anaerobic conditions. They were also discovered to have high sensitivity to transition metal ions and physiological flavin derivatives. These properties make flavin-binding fluorescent proteins (FPs) a perspective platform for biosensor development. However, brightness of currently available flavin-binding FPs is limited compared to GFP-like FPs creating a need for their further enhancement and optimization. In this study, we applied a directed molecular evolution approach to develop a pair of flavin-binding FPs, named miniGFP1 and miniGFP2. The miniGFP proteins are characterized by cyan-green fluorescence with excitation/emission maxima at 450/499 nm and a molecular size of ∼13 kDa. We carried out systematic benchmarking of miniGFPs in Escherichia coli and cultured mammalian cells against spectrally similar FPs including GFP-like FP, bilirubin-binding FP, and bright flavin-binding FPs. The miniGFPs proteins exhibited improved photochemical properties compared to other flavin-binding FPs enabling long-term live cell imaging. We demonstrated the utility of miniGFPs for live cell imaging in bacterial culture under anaerobic conditions and in CHO cells under hypoxia. The miniGFPs’ fluorescence was highly sensitive to Cu(II) ions in solution with K(d) values of 67 and 68 nM for miniGFP1 and miniGFP2, respectively. We also observed fluorescence quenching of miniGFPs by the reduced form of Cu(I) suggesting its potential application as an optical indicator for Cu(I) and Cu(II). In addition, miniGFPs showed the ability to selectively bind exogenous flavin mononucleotide demonstrating a potential for utilization as a selective fluorescent flavin indicator. Altogether, miniGFPs can serve as a multisensing platform for fluorescence biosensor development for in vitro and in-cell applications.
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spelling pubmed-96188082022-11-01 Enhanced small green fluorescent proteins as a multisensing platform for biosensor development Liang, Guo-Teng Lai, Cuixin Yue, Zejun Zhang, Hanbin Li, Danyang Chen, Zhong Lu, Xingyu Tao, Liang Subach, Fedor V. Piatkevich, Kiryl D. Front Bioeng Biotechnol Bioengineering and Biotechnology Engineered light, oxygen, and voltage (LOV)-based proteins are able to fluoresce without oxygen requirement due to the autocatalytic incorporation of exogenous flavin as a chromophore thus allowing for live cell imaging under hypoxic and anaerobic conditions. They were also discovered to have high sensitivity to transition metal ions and physiological flavin derivatives. These properties make flavin-binding fluorescent proteins (FPs) a perspective platform for biosensor development. However, brightness of currently available flavin-binding FPs is limited compared to GFP-like FPs creating a need for their further enhancement and optimization. In this study, we applied a directed molecular evolution approach to develop a pair of flavin-binding FPs, named miniGFP1 and miniGFP2. The miniGFP proteins are characterized by cyan-green fluorescence with excitation/emission maxima at 450/499 nm and a molecular size of ∼13 kDa. We carried out systematic benchmarking of miniGFPs in Escherichia coli and cultured mammalian cells against spectrally similar FPs including GFP-like FP, bilirubin-binding FP, and bright flavin-binding FPs. The miniGFPs proteins exhibited improved photochemical properties compared to other flavin-binding FPs enabling long-term live cell imaging. We demonstrated the utility of miniGFPs for live cell imaging in bacterial culture under anaerobic conditions and in CHO cells under hypoxia. The miniGFPs’ fluorescence was highly sensitive to Cu(II) ions in solution with K(d) values of 67 and 68 nM for miniGFP1 and miniGFP2, respectively. We also observed fluorescence quenching of miniGFPs by the reduced form of Cu(I) suggesting its potential application as an optical indicator for Cu(I) and Cu(II). In addition, miniGFPs showed the ability to selectively bind exogenous flavin mononucleotide demonstrating a potential for utilization as a selective fluorescent flavin indicator. Altogether, miniGFPs can serve as a multisensing platform for fluorescence biosensor development for in vitro and in-cell applications. Frontiers Media S.A. 2022-10-17 /pmc/articles/PMC9618808/ /pubmed/36324888 http://dx.doi.org/10.3389/fbioe.2022.1039317 Text en Copyright © 2022 Liang, Lai, Yue, Zhang, Li, Chen, Lu, Tao, Subach and Piatkevich. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Liang, Guo-Teng
Lai, Cuixin
Yue, Zejun
Zhang, Hanbin
Li, Danyang
Chen, Zhong
Lu, Xingyu
Tao, Liang
Subach, Fedor V.
Piatkevich, Kiryl D.
Enhanced small green fluorescent proteins as a multisensing platform for biosensor development
title Enhanced small green fluorescent proteins as a multisensing platform for biosensor development
title_full Enhanced small green fluorescent proteins as a multisensing platform for biosensor development
title_fullStr Enhanced small green fluorescent proteins as a multisensing platform for biosensor development
title_full_unstemmed Enhanced small green fluorescent proteins as a multisensing platform for biosensor development
title_short Enhanced small green fluorescent proteins as a multisensing platform for biosensor development
title_sort enhanced small green fluorescent proteins as a multisensing platform for biosensor development
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618808/
https://www.ncbi.nlm.nih.gov/pubmed/36324888
http://dx.doi.org/10.3389/fbioe.2022.1039317
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