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Intrinsically disordered protein biosensor tracks the physical-chemical effects of osmotic stress on cells.

Published version
Peer-reviewed

Type

Article

Change log

Authors

Cuevas-Velazquez, Cesar L  ORCID logo  https://orcid.org/0000-0002-6629-6444
Vellosillo, Tamara 
Guadalupe, Karina 
Schmidt, Hermann Broder  ORCID logo  https://orcid.org/0000-0002-0750-8419

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.

Description

Funder: Howard Hughes Medical Institute

Keywords

Cell Line, Tumor, Osteoblasts, Humans, Escherichia coli, Saccharomyces cerevisiae, Arabidopsis, Water, Molecular Chaperones, Arabidopsis Proteins, Recombinant Proteins, Fluorescence Resonance Energy Transfer, Biosensing Techniques, Gene Expression, Binding Sites, Protein Conformation, Protein Binding, Kinetics, Osmolar Concentration, Osmotic Pressure, Thermodynamics, Models, Molecular, Protein Interaction Domains and Motifs, Intrinsically Disordered Proteins

Journal Title

Nature communications

Conference Name

Journal ISSN

2041-1723

Volume Title

12

Publisher

Sponsorship
NIGMS NIH HHS (R35 GM137926)