Light-dependent modulation of protein localization and function in living bacteria cells

Most bacteria lack membrane-enclosed organelles and rely on macromolecular scaffolds at different subcellular locations to recruit proteins for specific functions. Here, we demonstrate that the optogenetic CRY2-CIB1 system from Arabidopsis thaliana can be used to rapidly direct proteins to different subcellular locations with varying efficiencies in live Escherichia coli cells, including the nucleoid, the cell pole, the membrane, and the midcell division plane. Such light-induced re-localization can be used to rapidly inhibit cytokinesis in actively dividing E. coli cells. We further show that CRY2-CIBN binding kinetics can be modulated by green light, adding a new dimension of control to the system. Finally, we test this optogenetic system in three additional bacterial species, Bacillus subtilis, Caulobacter crescentus, and Streptococcus pneumoniae, providing important considerations for this system's applicability in bacterial cell biology.

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Publication Details

Journal
Nature Communications
Published
2024-12-30
DOI
https://doi.org/10.1038/s41467-024-54974-9
Citations
6
Primary Topic
Light effects on plants
Type
article
Field-Weighted Citation Impact
3.60

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article

Light-dependent modulation of protein localization and function in living bacteria cells

Ho‐Ching Tiffany Tsui, Malcolm E. Winkler, Joshua W. McCausland, Erin D. Goley et al.
6 citations
Nature Communications
Light effects on plants
3.60
article

Light-dependent modulation of protein localization and function in living bacteria cells

Ho‐Ching Tiffany Tsui, Malcolm E. Winkler, Joshua W. McCausland, Erin D. Goley, Jie Xiao, Ryan McQuillen, Kevin E. Bruce, Amilcar J. Perez, Erika Smith, Sylvia Chareyre, Kumaran S. Ramamurthi, Christopher H. Bohrer, Yin Mon Hla, Xinxing Yang
article en
6 citations

Abstract

Most bacteria lack membrane-enclosed organelles and rely on macromolecular scaffolds at different subcellular locations to recruit proteins for specific functions. Here, we demonstrate that the optogenetic CRY2-CIB1 system from Arabidopsis thaliana can be used to rapidly direct proteins to different subcellular locations with varying efficiencies in live Escherichia coli cells, including the nucleoid, the cell pole, the membrane, and the midcell division plane. Such light-induced re-localization can be used to rapidly inhibit cytokinesis in actively dividing E. coli cells. We further show that CRY2-CIBN binding kinetics can be modulated by green light, adding a new dimension of control to the system. Finally, we test this optogenetic system in three additional bacterial species, Bacillus subtilis, Caulobacter crescentus, and Streptococcus pneumoniae, providing important considerations for this system's applicability in bacterial cell biology.

Nature CommunicationsVol. 15(1)
National Institutes of Health (US), Johns Hopkins University (US), Johns Hopkins Medicine (US), Indiana University Bloomington (US), National Cancer Institute (US)
National Institutes of Health, National Institute of General Medical Sciences
Zero hunger
Openalex Percentile: Top 7%
Light effects on plants
3.60
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