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Intrinsically disordered regions (IDRs) are flexible protein domains that modify their conformation in response to environmental changes. Ensemble fluorescence resonance energy transfer (FRET) can estimate protein dimensions under different conditions. We present a FRET approach to assess IDR structural sensitivity in living Saccharomyces cerevisiae cells under hyperosmotic stress.
Intrinsically disordered regions (IDRs) are protein domains that participate in crucial cellular processes. During stress conditions, the physicochemical properties of the cellular environment change, directly impacting the conformational ensemble of IDRs. IDRs are inherently sensitive to environmental perturbations. Studying how the physicochemical properties of the cell regulate the conformational ensemble of IDRs is essential for understanding the environmental control of their function. Here, we describe a step-by-step method for measuring the structural sensitivity of IDRs in living Saccharomyces cerevisiae cells in response to hyperosmotic stress conditions. We present the use of ensemble fluorescence resonance energy transfer (FRET) to estimate how the global dimensions of IDRs change during a progressive increase of hyperosmotic stress imposed on cells with any osmolyte. In addition, we provide a script for processing fluorescence measurements and comparing structural sensitivity for different IDRs. By following this method, researchers can obtain valuable insights into the conformational changes that IDRs undergo in the complex intracellular milieu upon changing environments.
Intrinsically disordered regions (IDRs) are critical components in cellular processes1. In combination with structured domains, IDRs are essential for protein functions. The amino acid composition of IDRs is biased, represented mainly by charged, hydrophilic, and small residues. Because of this property, IDRs are considered low complexity domains2,3. Numerous IDRs have garnered attention, primarily because these regions play a crucial role in pathological conditions, particularly neurodegenerative diseases. Such diseases are characterized by self-assembly and subsequent extracellular or....
1. Plasmid construct
After transforming yeast cells with pDRFLIP38-AtLEA4-5 plasmid, the fluorescence of the positive transformants was observed with a blue light transilluminator and a filter (Figure 1). Preparing the different solutions to induce hyperosmotic stress is time-consuming, so we suggest following the 96-well template of Figure 2. Immediately after the hyperosmotic stress treatment with varying concentrations of sodium chloride, the fluorescence emission spectra were ac.......
The method presented here offers a way to obtain insights into how the global dimensions of the ensemble of IDRs sense and respond to environmental perturbations. This method relies on a genetically encoded construct and requires no additional components beyond a plasmid stable expression in yeast cells, making it adaptable for potential applications in other cell types. Moreover, it is versatile for exploring other physicochemical perturbations that eukaryotic cells experience during their life cycle21.......
We thank members of the Cuevas-Velazquez lab for the critical review of the manuscript. This work was supported by Programa de Apoyo a Proyectos de Investigación e Innovación Tecnológica, Dirección General de Asuntos del Personal Académico, Universidad Nacional Autónoma de México (UNAM-PAPIIT) project number IA203422; Consejo Nacional de Humanidades, Ciencias y Tecnología (CONAHCYT), project number 252952; and Programa de Apoyo a la Investigación y el Posgrado, Facultad de Química, Universidad Nacional Autónoma de México, Grant 5000-9182. CET (CVU 1083636) and CAPD (CVU 1269643) acknowledge CONAHCYT for their....
Name | Company | Catalog Number | Comments |
96-well plate | Greiner Bio-One | 655096 | |
Agar | Sigma-Aldrich | 5040 | |
BglII | New England BioLabs | R0144S | |
BJ5465 cells | American Type Culture Collection | 208289 | |
Buffer MES 50 mM | Sigma-Aldrich | M8250 | |
Buffer Tris-HCl 10 mM | Invitrogen | 15506017 | |
EDTA 1 mM | Merck | 108452 | |
Falcon tubes | Corning | 352057 | |
LB media | Sigma-Aldrich | L2897 | |
Lithium acetate 0.1 M | Sigma-Aldrich | L6883 | |
Low Melt Agarose | GOLDBIO | A-204-25 | |
Microcentrifuge | eppendorf | 5452000010 | |
Miniprep kit | ZymoPure | D4210 | |
NaOH 0.02 M | Merck | 106462 | |
PEG 3,350 40% | Sigma-Aldrich | 1546547 | |
plasmid pDRFLIP38-AtLEA4-5 | addgene | 178189 | |
Plate reader | BMG LABTECH | CLARIOstar Plus | |
SacI | New England BioLabs | R3156S | |
Salmon sperm DNA 2 mg/mL | Thermo Fisher Scientific | 15632011 | |
SD-Ura | Sigma-Aldrich | Y1501 | |
Sodium cloride | Sigma-Aldrich | S9888 | |
Taq polymesare | Promega | M5123 | |
Transiluminator | Accuris instruments | E4000 | |
UV-Visible spectrophotometer | Thermo Fisher Scientific | Biomate3 | |
YPD media | Sigma-Aldrich | Y1500 |
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