Author
Listed:
- Cesar L. Cuevas-Velazquez
(Stanford University
Carnegie Institution for Science
Instituto de Biotecnología, Universidad Nacional Autónoma de México
Facultad de Química, Universidad Nacional Autónoma de México)
- Tamara Vellosillo
(Stanford University
Carnegie Institution for Science)
- Karina Guadalupe
(Center for Cellular and Biomolecular Machines (CCBM), University of California
Chemistry and Chemical Biology Program, University of California)
- Hermann Broder Schmidt
(Stanford University School of Medicine)
- Feng Yu
(Center for Cellular and Biomolecular Machines (CCBM), University of California
Quantitative Systems Biology Program, University of California)
- David Moses
(Center for Cellular and Biomolecular Machines (CCBM), University of California
Chemistry and Chemical Biology Program, University of California)
- Jennifer A. N. Brophy
(Stanford University
Carnegie Institution for Science)
- Dante Cosio-Acosta
(Instituto de Biotecnología, Universidad Nacional Autónoma de México)
- Alakananda Das
(Stanford University)
- Lingxin Wang
(Stanford University)
- Alexander M. Jones
(Sainsbury Laboratory, Cambridge University)
- Alejandra A. Covarrubias
(Instituto de Biotecnología, Universidad Nacional Autónoma de México)
- Shahar Sukenik
(Center for Cellular and Biomolecular Machines (CCBM), University of California
Chemistry and Chemical Biology Program, University of California
Quantitative Systems Biology Program, University of California)
- José R. Dinneny
(Stanford University
Carnegie Institution for Science)
Abstract
Cell homeostasis is perturbed when dramatic shifts in the external environment cause the physical-chemical properties inside the cell to change. Experimental approaches for dynamically monitoring these intracellular effects are currently lacking. Here, we leverage the environmental sensitivity and structural plasticity of intrinsically disordered protein regions (IDRs) to develop a FRET biosensor capable of monitoring rapid intracellular changes caused by osmotic stress. The biosensor, named SED1, utilizes the Arabidopsis intrinsically disordered AtLEA4-5 protein expressed in plants under water deficit. Computational modeling and in vitro studies reveal that SED1 is highly sensitive to macromolecular crowding. SED1 exhibits large and near-linear osmolarity-dependent changes in FRET inside living bacteria, yeast, plant, and human cells, demonstrating the broad utility of this tool for studying water-associated stress. This study demonstrates the remarkable ability of IDRs to sense the cellular environment across the tree of life and provides a blueprint for their use as environmentally-responsive molecular tools.
Suggested Citation
Cesar L. Cuevas-Velazquez & Tamara Vellosillo & Karina Guadalupe & Hermann Broder Schmidt & Feng Yu & David Moses & Jennifer A. N. Brophy & Dante Cosio-Acosta & Alakananda Das & Lingxin Wang & Alexand, 2021.
"Intrinsically disordered protein biosensor tracks the physical-chemical effects of osmotic stress on cells,"
Nature Communications, Nature, vol. 12(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-25736-8
DOI: 10.1038/s41467-021-25736-8
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