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 Investigaci&#243;n e Innovaci&#243;n Tecnol&#243;gica, Direcci&#243;n General de Asuntos del Personal Acad&#233;mico, Universidad Nacional Aut&#243;noma de M&#233;xico (UNAM-PAPIIT) project number IA203422; Consejo Nacional de Humanidades, Ciencias y Tecnolog&#237;a (CONAHCYT), project number 252952; and Programa de Apoyo a la Investigaci&#243;n y el Posgrado, Facultad de Qu&#237;mica, Universidad Nacional Aut&#243;noma de M&#233;xico, Grant 5000-9182. CET (CVU 1083636) and CAPD (CVU 1269643) acknowledge CONAHCYT for their M.Sc. Scholarship.

1. Plasmid construct
<ol>
	<li>Amplify the open reading frame (ORF) that codes for the desired IDR by polymerase chain reaction (PCR). Do not include the stop codon since the ORF will be flanked by the genes that encode the fluorescent proteins. For the amplification, design primers with the SacI (5&#39;) and BglII (3&#39;) restriction sites. 
	NOTE: For the representative results section, we used AtLEA4-5 as the selected IDR. We amplified the ORF of AtLEA4-5 from the pTrc99A-AtLEA4-5 plasmid12.</li>
	<li>Digest the ORF PCR product by consecutive restriction with SacI and BglII enzymes13.</li>
	<li>Obtain the commercial plasmid pDRFLIP38-AtLEA4-5 (#178189) from Addgene (https://www.addgene.org/178189/).</li>
	<li>Conduct a consecutive restriction using SacI and BglII enzymes to remove the AtLEA4-5 ORF from the pDRFLIP38-AtLEA4-5 plasmid, leaving an open plasmid containing the FRET pair13.</li>
	<li>Purify the digested DNA fragments using gel recovery from an agarose gel electrophoresis14. Ligate the restricted fragments using DNA ligase15.</li>
	<li>Transform the cloning reaction into competent Escherichia coli cells (DH5&#945; or related strains) and select in Luria-Bertani (LB) plates containing 50 &#181;g/mL ampicillin16. Grow overnight (ON) at 37 &#176;C.</li>
	<li>Isolate and grow at least five transformed colonies in a new plate and genotype by PCR17. Purify the plasmid DNA from a positive transformed colony using standard miniprep methods18.</li>
	<li>Verify the extraction and integrity of the plasmid DNA using agarose gel electrophoresis19. Verify the correct cloning of the construct using Sanger sequencing20.</li>
</ol>
2. Plasmid expression in yeast cells
NOTE: Use standard aseptic techniques to perform the following steps. Use a culture laminar flow hood or a lighter.
<ol>
	<li>Inoculate a streak of S. cerevisiae BJ5465 (ATCC: 208289) strain into 3 mL of Yeast Peptone Dextrose (YPD) medium and grow ON&#160;at 30 &#176;C and 200 rpm. 
	NOTE: BJ5465 is a protease-deficient (CH1) strain recommended for working with IDRs. Other S. cerevisiae strains can be tested and used.</li>
	<li>Centrifuge 1 mL of the overnight saturated (OD600 ~ 3-4) yeast culture at 14,000 x g for 1 min. Carefully remove the supernatant by pipetting.</li>
	<li>Resuspend the pellet in 1 mL of Tris-EDTA (TE) buffer (pH 7.5) by gently flicking the tube. Centrifuge at 14,000 x g for 1 min and carefully remove the supernatant.</li>
	<li>Resuspend the pellet in 500 &#181;L of Lazy Bones buffer (40% w/v PEG 3,350; 100&#160;mM lithium acetate; 10 mM Tris-HCl; 1 mM EDTA; pH 7.5) by pipetting. Add 25 &#181;L of boiled (100 &#176;C for 5 min, followed by cooling on ice for 5 min) salmon sperm DNA (2 mg/mL) to the resuspended yeast cells.</li>
	<li>Add 100 ng of the plasmid DNA to the mixture and vortex the mixture for 1 min to ensure thorough mixing. Allow the mixture to stand at room temperature for 1-2 h.</li>
	<li>Heat shock the yeast mixture at 42 &#176;C for 12 min, then cool on ice for another 12 min. Centrifuge the tube at 14 000 x g for 1 min and carefully remove the supernatant.</li>
	<li>Resuspend the pellet in 1 mL of TE buffer (pH 7.5). Plate 100 &#181;L of the transformed cells onto Yeast Synthetic-dropout Medium without uracil (SD-ura) plates supplemented with 15 g/L agar.</li>
	<li>Incubate plates at 30 &#176;C for 2-3 days (Figure 1). Streak at least five yeast transformants in a new plate and grow ON.</li>
</ol>
3. Validation of yeast transformants
<ol>
	<li>Pick a small portion of each transformant candidate by gently scraping and resuspending in 5 &#181;L of 20&#160;mM NaOH into individual PCR tubes.</li>
	<li>Heat the sample at 99 &#176;C for 10 min in a thermal cycler to lyse the cells and release the DNA into the solution. This step is crucial for preparing the DNA template for PCR.</li>
	<li>Transfer 1 &#181;L of the boiled sample to a separate PCR reaction mix containing the appropriate primers and PCR reagents for genotyping. We used the following primers: Forward primer: 5&#180;-AAATATACCCCAGCCTCGATCTAGA-3&#180;. Reverse primer: 5&#180;-GTAATACGACTCACTATAGGGCG-3&#180;.</li>
	<li>Set up a PCR reaction and validate the presence of the correct plasmid using agarose gel electrophoresis. Select one transformant for further experiments.</li>
</ol>
4. Preparation of yeast cell culture for FRET assay
<ol>
	<li>Inoculate a streak of the selected yeast transformant into 3 mL of liquid 1x SD-Ura medium. 
	NOTE: Do this procedure in a laminar flow hood and sterile material.</li>
	<li>Grow at 30 &#176;C, 200 rpm for at least 12 h to reach saturation. Measure the OD600. Growth should fall between OD600 = 1.0-2.0. 
	&#8203;NOTE: If OD600 is lower than 1.0, give cells more incubation time to grow. If OD600 exceeds 2.0, do not proceed and restart from step 4.1.</li>
</ol>
5. Yeast cell preparation for FRET assay
<ol>
	<li>Collect 2 mL of the overnight yeast culture and centrifuge at 14,000 x g at room temperature. Carefully remove the supernatant by pipetting.</li>
	<li>Resuspend the pellet in 1 mL of 50 mM 2-(N-Morpholino) ethanesulfonic acid (MES) buffer (pH 6).</li>
	<li>Centrifuge at 14,000 x g at room temperature. Remove the supernatant.</li>
	<li>Repeat steps 5.2 and 5.3. Resuspend yeast cells in 2 mL of MES buffer, pH 6 and pour the volume into a reagent reservoir.</li>
</ol>
6. Setting up the fluorescence measurements
NOTE: The present scanning is considered to be performed in a microplate reader with fluorescence mode.
<ol>
	<li>For basic settings, set the instrument as follows: Measurement type: Fluorescence Intensity (FI) spectrum; Microplate name: Greiner 96 F-bottom.</li>
	<li>For optic settings, set the instrument as follows: No. of wavelength scan points: 91; Excitation wavelength: 433 nm; Excitation bandwidth: 10 nm; Emission wavelength: 460 - 550; Step width: 1 nm; Emission bandwidth: 10 nm; Focal height obtained by autofocus; Focal height: 5 mm; Wavelength used for gain: 490 nm.</li>
	<li>For general settings, set the instrument as follows: Settling time: 0.1 s; Reading direction: unidirectional, horizontal left to right, top to bottom. 
	&#8203;NOTE: The manually entered gain must be adjusted for every measurement using the well expected to display the highest fluorescence intensity levels throughout the wavelength scan.</li>
</ol>
7. Preparation of hypertonic solutions and fluorescence measurements
<ol>
	<li>Prepare solutions of 0 M, 0.2 M, 0.4 M, 0.6 M, 0.8 M, 1 M, 1.5 M, and 2 M NaCl in a 96-well clear-bottom black plate. The final volume in each well will be 200 &#181;L (150 &#181;L of osmolyte solution + 50 &#181;L of yeast cell suspension). 
	NOTE: Other osmolytes can be used to induce hyperosmotic stress. All the solutions must be prepared in 50 mM MES buffer pH 6.</li>
	<li>Load 150 &#181;L of 50 mM MES buffer, pH 6 in first three wells of row A (A1, A2, A3) and in the subsequent wells, add 150 &#181;L of the corresponding solution in increasing order from left to right (Figure 2). To test all the concentrations suggested, continue the loading in row B. 
	NOTE: This setting considers the measurements of 3 technical replicates for each concentration.</li>
	<li>Use a 12-channel micropipette to transfer 50 &#181;L of washed yeast cells to each well. Yeast cells tend to sediment to the bottom of the reservoir. Make sure to resuspend the yeast suspension thoroughly by pipetting up and down before transferring the cells.</li>
	<li>Load cells into the 96-well plate containing the different solutions and mix well by pipetting up and down at least 4x.</li>
	<li>Measure fluorescence intensity emission spectra immediately for the desired wells in a microplate reader with the specification settings of step 6. Repeat the procedure for every IDR to be tested in the FRET assay.</li>
	<li>Optional step. If available, measure a donor-only construct (pDRFLIP38-mCerulean3) following the steps described here. 
	NOTE: We recommended performing this step to calculate each condition&#39;s FRET efficiency. If the reader cannot perform this step, FRET can be calculated using the FRET ratio method. Both methods for FRET calculations are explained in steps 8 and 9.</li>
	<li>Perform at least three replicates on three independent days for every construct.</li>
</ol>
8. Data processing using the FRET efficiency method
NOTE: For readers with knowledge of the R programming language, we provide a set of R scripts to perform data processing described in this section. Scripts can be found at&#160;https://github.com/Kaz-bits/cuevaslab-procotols/tree/main/FRET. Follow the instructions in the README file.
<ol>
	<li>Export data as .xlsx&#160;files from the microplate reader.</li>
	<li>Normalize fluorescence intensity values at every scan wavelength to the isosbestic point of the FRET pair used. 
	NOTE: This step is necessary for comparing the spectra of all conditions tested. The isosbestic point of mCerulean3 and Citrine FRET pair is 515 nm. For example, obtain the ratio of fluorescence intensity values of 460 nm/515 nm, 461 nm/515 nm, 462 nm/515 nm, and so on.</li>
	<li>Calculate the mean for every technical replicate once the fluorescence values are normalized. In total, there should be a column for every condition of hyperosmotic stress.</li>
	<li>Visualize all the fluorescence intensity spectra in the same plot (Figure 3). Each spectrum should display a combination of the fluorescence emission spectra of individual mCerulean3 and Citrine. In rare cases, where the FRET efficiency is 0, only the donor fluorescence emission spectrum will be observed, or when FRET efficiency is 1, only the acceptor fluorescence will be observed. The fluorescence emission peak for mCerulean3 (donor) is 475 nm, and the fluorescence emission peak for Citrine (acceptor) is 525 nm.</li>
	<li>Determine if the fluorescence measurement displays a typical FRET change in response to hyperosmotic stress. If the conformation of the IDR is sensitive to the treatment, this will reflect as a change in FRET efficiency. A typical change in FRET efficiency will couple a decrease in the fluorescence intensity of the donor with an increase in the fluorescence intensity of the acceptor or vice versa.</li>
	<li>Quantify the FRET efficiency (EFRET). Obtain the donor (mCerulean3) normalized peak values (475 nm/515 nm) for the IDR construct and the donor-only construct for every condition of hyperosmotic stress. Use the mean normalized peak values of the technical replicates. Perform this operation for each of the three independent replicates. Calculate EFRET with the following formula: 
	<img alt="Equation 1" src="/files/ftp_upload/66275/66275eq01.jpg" style="margin: auto;" /> 
	Where IDA is the ratio 475 nm/515 nm from the IDR construct (FRET pair construct), and ID is the ratio 475 nm/515 nm from the donor-only construct.</li>
	<li>Compare FRET efficiencies. Normalize the EFRET values of every hyperosmotic stress condition to the EFRET of the non-stress condition (for example, 0 M NaCl). Make comparisons using a box plot or a smooth curve plot. Perform a One-way ANOVA followed by a post hoc Tukey statistical test (p-values: *p &#60; 0.05, **p &#60; 0.01, ***p &#60; 0.001, ****p &#60; 0.0001).</li>
</ol>
9. Data processing using the FRET ratio method
NOTE: If donor-only measurements cannot be acquired, perform the FRET ratio method. This method compares the FRET ratio across the different hyperosmotic stress conditions. Steps 7.1 to 7.5 should be performed before the steps of this section to validate a typical FRET behavior. For readers with knowledge of the R programming language, we provide a set of R scripts to perform data processing described in this section. Scripts can be found at&#160;https://github.com/Kaz-bits/cuevaslab-procotols/tree/main/FRET. Follow the instructions in the README file.
<ol>
	<li>Extract data at 475 nm and 525 nm from the xlsx&#160;file previously exported from the microplate reader. These values correspond to the fluorescence emission peak for mCerulean3 (donor, DxDm) and the fluorescence emission peak for Citrine (acceptor, DxAm) when the donor fluorophore is excited (433 nm).</li>
	<li>Normalize fluorescence intensity values at 475 nm and 525 nm to the isosbestic point of the FRET pair used. The isosbestic point of mCerulean3 and Citrine FRET pair is 515 nm. Obtain the FRET ratio (DxAm/DxDm).</li>
	<li>Compare FRET ratios. Normalize the DxAm/DxDm values of every hyperosmotic stress condition to the mean DxAm/DxDm of the non-stress condition (for example, 0 M NaCl). Make comparisons using a box plot or a smooth curve plot (Figure 4 and Figure 5). Perform a One-way ANOVA followed by a post hoc Tukey statistical test (p-values: *p &#60; 0.05, **p &#60; 0.01, ***p &#60; 0.001, ****p &#60; 0.0001).</li>
</ol>

FRET Analysis of IDR Structural Sensitivity to Study Hyperosmotic Stress in Yeast

<ol>
	<li>Wright, P. E., Dyson, H. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Intrinsically+disordered+proteins+in+cellular+signalling+and+regulation.">Intrinsically disordered proteins in cellular signalling and regulation.</a> Nat Rev Mol Cell Biol. 16 (1), 18-29 (2015).</li><li>Covarrubias, A. A., Romero-P&#233;rez, P. S., Cuevas-Velazquez, C. L., Rend&#243;n-Luna, D. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+functional+diversity+of+structural+disorder+in+plant+proteins.">The functional diversity of structural disorder in plant proteins.</a> Arch Biochem Biophys. 680, 108229 (2019).</li><li>Ahmed, S. S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Characterization+of+intrinsically+disordered+regions+in+proteins+informed+by+human+genetic+diversity.">Characterization of intrinsically disordered regions in proteins informed by human genetic diversity.</a> PLoS Comput Biol. 18 (3), e1009911 (2022).</li><li>Birol, M., Melo, A. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Untangling+the+conformational+polymorphism+of+disordered+proteins+associated+with+neurodegeneration+at+the+single-molecule+level.">Untangling the conformational polymorphism of disordered proteins associated with neurodegeneration at the single-molecule level.</a> Front Mol Neurosci. 12, 309 (2019).</li><li>Moses, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Revealing+the+hidden+sensitivity+of+intrinsically+disordered+proteins+to+their+chemical+environment.">Revealing the hidden sensitivity of intrinsically disordered proteins to their chemical environment.</a> J Phys Chem Lett. 11 (23), 10131-10136 (2020).</li><li>Cuevas-Velazquez, C. L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Intrinsically+disordered+protein+biosensor+tracks+the+physical-chemical+effects+of+osmotic+stress+on+cells.">Intrinsically disordered protein biosensor tracks the physical-chemical effects of osmotic stress on cells.</a> Nat Commun. 12 (1), 5438 (2021).</li><li>Holehouse, A. S., Sukenik, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Controlling+structural+bias+in+intrinsically+disordered+proteins+using+solution+space+scanning.">Controlling structural bias in intrinsically disordered proteins using solution space scanning.</a> J Chem Theory Comput. 16 (3), 1794-1805 (2020).</li><li>Martin, E. W., Hopkins, J. B., Mittag, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Small-angle+X-ray+scattering+experiments+of+monodisperse+intrinsically+disordered+protein+samples+close+to+the+solubility+limit.">Small-angle X-ray scattering experiments of monodisperse intrinsically disordered protein samples close to the solubility limit.</a> Methods Enzymol. 646, 185-222 (2021).</li><li>Miles, A. J., Drew, E. D., Wallace, B. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=DichroIDP:+a+method+for+analyses+of+intrinsically+disordered+proteins+using+circular+dichroism+spectroscopy.">DichroIDP: a method for analyses of intrinsically disordered proteins using circular dichroism spectroscopy.</a> Commun Biol. 6 (1), 823 (2023).</li><li>Kaminski, C. F., Rees, E. J., Schierle, G. S. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+quantitative+protocol+for+intensity-based+live+cell+FRET+imaging.">A quantitative protocol for intensity-based live cell FRET imaging.</a> Method Mol Biol. 1076, 445-454 (2014).</li><li>Moses, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Structural+biases+in+disordered+proteins+are+prevalent+in+the+cell.">Structural biases in disordered proteins are prevalent in the cell.</a> bioRxiv. , (2022).</li><li>Cuevas-Velazquez, C. L., Saab-Rinc&#243;n, G., Reyes, J. L., Covarrubias, A. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+Unstructured+N-terminal+Region+of+Arabidopsis+Group+4+Late+Embryogenesis+Abundant+(LEA)+Proteins+Is+Required+for+Folding+and+for+Chaperone-like+Activity+under+Water+Deficit.">The Unstructured N-terminal Region of Arabidopsis Group 4 Late Embryogenesis Abundant (LEA) Proteins Is Required for Folding and for Chaperone-like Activity under Water Deficit.</a> J Biol Chem. 291 (20), 10893-10903 (2016).</li><li>JoVE Science Education Database. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Restriction enzyme digests. , (2023).</li><li>JoVE Science Education Database. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Gel purification. , (2023).</li><li>JoVE Science Education Database. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> DNA ligation reactions. , (2023).</li><li>JoVE Science Education Database. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Bacterial transformation using heat Ssock and competent cells. , (2023).</li><li>JoVE Science Education Database. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> PCR: Principle, instrumentation, and applications. , (2023).</li><li>JoVE Science Education Database. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Plasmid purification. , (2023).</li><li>JoVE Science Education Database. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> DNA gel electrophoresis. , (2023).</li><li>JoVE Core Molecular Biology. Sanger/chain termination sequencing using dideoxynucleotides - Concept Available from: <a target="_blank" href="https://app.jove.com/science-education/v/12020/sanger-sequencing">https://app.jove.com/science-education/v/12020/sanger-sequencing</a> (2023)</li><li>Theillet, F. X., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Physicochemical+properties+of+cells+and+their+effects+on+intrinsically+disordered+proteins+(IDPs).">Physicochemical properties of cells and their effects on intrinsically disordered proteins (IDPs).</a> Chem Rev. 114 (13), 6661-6714 (2014).</li><li>Brutscher, B., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=NMR+methods+for+the+study+of+instrinsically+disordered+proteins+structure,+dynamics,+and+interactions:+General+overview+and+practical+guidelines.">NMR methods for the study of instrinsically disordered proteins structure, dynamics, and interactions: General overview and practical guidelines.</a> Adv Exp Med Biol. 870, 49-122 (2015).</li><li>Metskas, L. A., Rhoades, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Single-molecule+FRET+of+intrinsically+disordered+proteins.">Single-molecule FRET of intrinsically disordered proteins.</a> Annu Rev Phys Chem. 71, 391-414 (2020).</li><li>Roebroek, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Simultaneous+readout+of+multiple+FRET+pairs+using+photochromism.">Simultaneous readout of multiple FRET pairs using photochromism.</a> Nat Commun. 12 (1), 2005 (2021).</li><li>Algar, W. R., Hildebrandt, N., Vogel, S. S., Medintz, I. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=FRET+as+a+biomolecular+research+tool+-+understanding+its+potential+while+avoiding+pitfalls.">FRET as a biomolecular research tool - understanding its potential while avoiding pitfalls.</a> Nat Methods. 16 (9), 815-829 (2019).</li><li>Lyon, A. S., Peeples, W. B., Rosen, M. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+framework+for+understanding+the+functions+of+biomolecular+condensates+across+scales.">A framework for understanding the functions of biomolecular condensates across scales.</a> Nat Rev Mol Cell Biol. 22 (3), 215-235 (2021).</li><li>Belott, C., Janis, B., Menze, M. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Liquid-liquid+phase+separation+promotes+animal+desiccation+tolerance.">Liquid-liquid phase separation promotes animal desiccation tolerance.</a> Proc Natl Acad Sci U S A. 117 (44), 27676-27684 (2020).</li><li>Miermont, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Severe+osmotic+compression+triggers+a+slowdown+of+intracellular+signaling,+which+can+be+explained+by+molecular+crowding.">Severe osmotic compression triggers a slowdown of intracellular signaling, which can be explained by molecular crowding.</a> Proc Natl Acad Sci U S A. 110 (14), 5725-5730 (2013).</li><li>Saito, H., Posas, F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Response+to+hyperosmotic+stress.">Response to hyperosmotic stress.</a> Genetics. 192 (2), 289-318 (2012).</li><li>Selenko, P., Wagner, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Looking+into+live+cells+with+in-cell+NMR+spectroscopy.">Looking into live cells with in-cell NMR spectroscopy.</a> J Struct Biol. 158 (2), 244-253 (2007).</li><li>Cattani, J., Subramaniam, V., Drescher, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Room-temperature+in-cell+EPR+spectroscopy:+alpha-Synuclein+disease+variants+remain+intrinsically+disordered+in+the+cell.">Room-temperature in-cell EPR spectroscopy: alpha-Synuclein disease variants remain intrinsically disordered in the cell.</a> Phys Chem Chem Phys. 19 (28), 18147-18151 (2017).</li><li>Beveridge, R., Chappuis, Q., Macphee, C., Barran, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mass+spectrometry+methods+for+intrinsically+disordered+proteins.">Mass spectrometry methods for intrinsically disordered proteins.</a> Analyst. 138 (1), 32-42 (2013).</li><li>Beveridge, R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Ion+mobility+mass+spectrometry+uncovers+the+impact+of+the+patterning+of+oppositely+charged+residues+on+the+conformational+distributions+of+intrinsically+disordered+proteins.">Ion mobility mass spectrometry uncovers the impact of the patterning of oppositely charged residues on the conformational distributions of intrinsically disordered proteins.</a> J Am Chem Soc. 141 (12), 4908-4918 (2019).</li></ol>

The authors declare no conflicts of interest.

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...

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 intracellular deposition of IDRs in neurons4. Examples of such IDRs include amyloid-&#946;&#160;(A&#946;) in Alzheimer&#39;s disease, huntingtin (HTT) in Huntington&#39;s disease, and TAR DNA-binding protein-43 (TDP-43) and fused in sarcoma (FUS) in amyotrophic lateral sclerosis and frontotemporal dementia4. The study of the structural rearrangements of IDRs in the context of disease has been significantly enhanced by spectroscopic methods, including fluorescence resonance energy transfer (FRET).
The hydrophilic and extended nature of IDRs makes them extremely sensitive to changes in the physicochemical properties of the solution environment5. The degree by which the conformational ensemble of IDRs is modified by the environment is called structural sensitivity5,6,7. Different techniques can be used to study the conformation and dynamics of IDRs, including circular dichroism (CD) and small-angle X-ray scattering (SAXS)8,9. Unfortunately, CD and SAXS require large quantities of purified proteins, so they are not appropriate for studies in cells. In contrast, FRET is a technique that measures the fluorescence intensity of two fluorescent molecules that specifically label one IDR, meaning that they can be monitored in complex mixtures such as living cells10. Dynamically measuring the structural sensitivity of IDRs in living cells is necessary for understanding how the environment regulates the conformation and function of the disordered proteome.
FRET is a powerful method for quantifying the structural sensitivity of IDRs, as well as globular and multidomain proteins in living cells. The method requires a construct consisting of an IDR of interest sandwiched between two fluorescent proteins (FP), known as a FRET pair. For this protocol, we suggest the use of mCerulean3 as the donor FP and Citrine as the acceptor FP, because of their large dynamic range, compared to other FPs reported in a previous study about IDRs sensitivity6. FRET has previously been exploited to measure the structural sensitivity of a plant IDR in different cellular contexts6. In addition, this technique has been used to characterize overall protein dimensions of IDRs by different research groups both in vitro and in vivo5,11.
Here, we describe the ensemble FRET method for studying the structural sensitivity of IDRs in living yeast (Saccharomyces cerevisiae) cells. We show representative results that are based in a plant IDR called AtLEA4-5. AtLEA4-5 is disordered in solution, but folds into &#945;-helix when macromolecular crowding is induced in vitro12. AtLEA4-5 is a good reference model for this method because it is relatively small (158 residues), disordered and sensitive to environmental perturbation as reported in silico and in vitro6,12. The method presented here can be scaled for high throughput approaches because yeast cells are easy to grow, and the treatment is applied in small volumes. In addition, small modifications to the protocol can be applied to other cellular systems such as bacteria and plant cells6. The protocol can be performed in any molecular biology laboratory with access to a microplate reader with fluorescence mode, an equipment available in most research institutions.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>96-well plate</td>
			<td>Greiner Bio-One</td>
			<td>655096</td>
			<td></td>
		</tr>
		<tr>
			<td>Agar</td>
			<td>Sigma-Aldrich</td>
			<td>5040</td>
			<td></td>
		</tr>
		<tr>
			<td>BglII</td>
			<td>New England BioLabs</td>
			<td>R0144S</td>
			<td></td>
		</tr>
		<tr>
			<td>BJ5465 cells</td>
			<td>American Type Culture Collection</td>
			<td>208289</td>
			<td></td>
		</tr>
		<tr>
			<td>Buffer MES 50 mM</td>
			<td>Sigma-Aldrich</td>
			<td>M8250</td>
			<td></td>
		</tr>
		<tr>
			<td>Buffer Tris-HCl 10 mM</td>
			<td>Invitrogen</td>
			<td>15506017</td>
			<td></td>
		</tr>
		<tr>
			<td>EDTA 1 mM</td>
			<td>Merck</td>
			<td>108452</td>
			<td></td>
		</tr>
		<tr>
			<td>Falcon tubes</td>
			<td>Corning</td>
			<td>352057</td>
			<td></td>
		</tr>
		<tr>
			<td>LB media</td>
			<td>Sigma-Aldrich</td>
			<td>L2897</td>
			<td></td>
		</tr>
		<tr>
			<td>Lithium acetate 0.1 M</td>
			<td>Sigma-Aldrich</td>
			<td>L6883</td>
			<td></td>
		</tr>
		<tr>
			<td>Low Melt Agarose</td>
			<td>GOLDBIO</td>
			<td>A-204-25</td>
			<td></td>
		</tr>
		<tr>
			<td>Microcentrifuge</td>
			<td>eppendorf</td>
			<td>5452000010</td>
			<td></td>
		</tr>
		<tr>
			<td>Miniprep kit</td>
			<td>ZymoPure</td>
			<td>D4210</td>
			<td></td>
		</tr>
		<tr>
			<td>NaOH 0.02 M</td>
			<td>Merck</td>
			<td>106462</td>
			<td></td>
		</tr>
		<tr>
			<td>PEG 3,350 40%</td>
			<td>Sigma-Aldrich</td>
			<td>1546547</td>
			<td></td>
		</tr>
		<tr>
			<td>plasmid pDRFLIP38-AtLEA4-5</td>
			<td>addgene</td>
			<td>178189</td>
			<td></td>
		</tr>
		<tr>
			<td>Plate reader</td>
			<td>BMG LABTECH</td>
			<td>CLARIOstar Plus</td>
			<td></td>
		</tr>
		<tr>
			<td>SacI</td>
			<td>New England BioLabs</td>
			<td>R3156S</td>
			<td></td>
		</tr>
		<tr>
			<td>Salmon sperm DNA 2 mg/mL</td>
			<td>Thermo Fisher Scientific</td>
			<td>15632011</td>
			<td></td>
		</tr>
		<tr>
			<td>SD-Ura</td>
			<td>Sigma-Aldrich</td>
			<td>Y1501</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium cloride</td>
			<td>Sigma-Aldrich</td>
			<td>S9888</td>
			<td></td>
		</tr>
		<tr>
			<td>Taq polymesare</td>
			<td>Promega</td>
			<td>M5123</td>
			<td></td>
		</tr>
		<tr>
			<td>Transiluminator</td>
			<td>Accuris instruments</td>
			<td>E4000</td>
			<td></td>
		</tr>
		<tr>
			<td>UV-Visible spectrophotometer</td>
			<td>Thermo Fisher Scientific</td>
			<td>Biomate3</td>
			<td></td>
		</tr>
		<tr>
			<td>YPD media</td>
			<td>Sigma-Aldrich</td>
			<td>Y1500</td>
			<td></td>
		</tr>
	</tbody>
</table>

estimation of structural sensitivity of intrinsically disordered regions in response to hyperosmotic stress in living cells using fret

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.

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...

Watch this Scientific Journal Video about Estimation of Structural Sensitivity of Intrinsically Disordered Regions in Response to Hyperosmotic Stress in Living Cells Using FRET at JoVE.com

Author Spotlight: Unlocking the World of Intrinsically Disordered Regions with Cellular Sensing and Responses

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.

Estimation of Structural Sensitivity of Intrinsically Disordered Regions in Response to Hyperosmotic Stress in Living Cells Using FRET

Intrinsically disordered regions (IDRs) are protein domains that participate in crucial cellular processes. During stress conditions, the physicochemical ...

estimation-structural-sensitivity-intrinsically-disordered-regions

Research

JoVE Journal

Biochemistry

871 Views.  Universidad Nacional Autónoma de México. 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.

Video: Author Spotlight: Unlocking the World of Intrinsically Disordered Regions with Cellular Sensing and Responses

Structural Information from Single-molecule FRET Experiments Using the Fast Nano-positioning System

Single-molecule F&#246;rster Resonance Energy Transfer (smFRET) can be used to obtain structural information on biomolecular complexes in real-time. Thereby, multiple smFRET measurements are used to localize an unknown dye position inside a protein complex by means of trilateration. In order to obtain quantitative information, the Nano-Positioning System (NPS) uses probabilistic data analysis to combine structural information from X-ray crystallography with single-molecule fluorescence data to calculate not only the most probable position but the complete three-dimensional probability distribution, termed posterior, which indicates the experimental uncertainty. The concept was generalized for the analysis of smFRET networks containing numerous dye molecules. The latest version of NPS, Fast-NPS, features a new algorithm using Bayesian parameter estimation based on Markov Chain Monte Carlo sampling and parallel tempering that allows for the analysis of large smFRET networks in a comparably short time. Moreover, Fast-NPS allows the calculation of the posterior by choosing one of five different models for each dye, that account for the different spatial and orientational behavior exhibited by the dye molecules due to their local environment.
Here we present a detailed protocol for obtaining smFRET data and applying the Fast-NPS. We provide detailed instructions for the acquisition of the three input parameters of Fast-NPS: the smFRET values, as well as the quantum yield and anisotropy of the dye molecules. Recently, the NPS has been used to elucidate the architecture of an archaeal open promotor complex. This data is used to demonstrate the influence of the five different dye models on the posterior distribution.

We present the setup and experimental procedure to obtain smFRET data from large donor-acceptor networks with a TIRF microscope. The step-by-step analysis of these measurements with the Bayesian inference software Fast-NPS yields high-resolved structural information via the application of adapted dye models.

Single-molecule F&#246;rster Resonance Energy Transfer (smFRET) can be used to obtain structural information on biomolecular complexes in real-time. ...

Using Scaffold Liposomes to Reconstitute Lipid-proximal Protein-protein Interactions In Vitro

Studies of integral membrane proteins in vitro are frequently complicated by the presence of a hydrophobic transmembrane domain. Further complicating these studies, reincorporation of detergent-solubilized membrane proteins into liposomes is a stochastic process where protein topology is impossible to enforce. This paper offers an alternative method to these challenging techniques that utilizes a liposome-based scaffold. Protein solubility is enhanced by deletion of the transmembrane domain, and these amino acids are replaced with a tethering moiety, such as a His-tag. This tether interacts with an anchoring group (Ni2+ coordinated by nitrilotriacetic acid (NTA(Ni2+)) for His-tagged proteins), which enforces a uniform protein topology at the surface of the liposome. An example is presented wherein the interaction between Dynamin-related protein 1 (Drp1) with an integral membrane protein, Mitochondrial Fission Factor (Mff), was investigated using this scaffold liposome method. In this work, we have demonstrated the ability of Mff to efficiently recruit soluble Drp1 to the surface of liposomes, which stimulated its GTPase activity. Moreover, Drp1 was able to tubulate the Mff-decorated lipid template in the presence of specific lipids. This example demonstrates the effectiveness of scaffold liposomes using structural and functional assays and highlights the role of Mff in regulating Drp1 activity.

Using Scaffold Liposomes to Reconstitute Lipid-proximal Protein-protein Interactions In Vitro

This paper describes a method for assessing the interactions and assemblies of integral membrane proteins in vitro with various partner factors in a lipid-proximal environment.

Studies of integral membrane proteins in vitro are frequently complicated by the presence of a hydrophobic transmembrane domain. Further complicating ...

Nuclear Magnetic Resonance Spectroscopy for the Identification of Multiple Phosphorylations of Intrinsically Disordered Proteins

Aggregates of the neuronal Tau protein are found inside neurons of Alzheimer's disease patients. Development of the disease is accompanied by increased, abnormal phosphorylation of Tau. In the course of the molecular investigation of Tau functions and dysfunctions in the disease, nuclear magnetic resonance (NMR) spectroscopy is used to identify the multiple phosphorylations of Tau. We present here detailed protocols of recombinant production of Tau in bacteria, with isotopic enrichment for NMR studies. Purification steps that take advantage of Tau's heat stability and high isoelectric point are described. The protocol for in vitro phosphorylation of Tau by recombinant activated ERK2 allows for generating multiple phosphorylations. The protein sample is ready for data acquisition at the issue of these steps. The parameter setup to start recording on the spectrometer is considered next. Finally, the strategy to identify phosphorylation sites of modified Tau, based on NMR data, is explained. The benefit of this methodology compared to other techniques used to identify phosphorylation sites, such as immuno-detection or mass spectrometry (MS), is discussed.

We describe here a method to identify multiple phosphorylations of an intrinsically disordered protein by Nuclear Magnetic Resonance Spectroscopy (NMR), using Tau protein as a case study. Recombinant Tau is isotopically enriched and modified in vitro by a kinase prior to data acquisition and analysis.

Aggregates of the neuronal Tau protein are found inside neurons of Alzheimer's disease patients. Development of the disease is accompanied by increased, ...

Sample Preparation for Mass Spectrometry-based Identification of RNA-binding Regions

Noncoding RNAs play important roles in several nuclear processes, including regulating gene expression, chromatin structure, and DNA repair. In most cases, the action of noncoding RNAs is mediated by proteins whose functions are in turn regulated by these interactions with noncoding RNAs. Consistent with this, a growing number of proteins involved in nuclear functions have been reported to bind RNA and in a few cases the RNA-binding regions of these proteins have been mapped, often through laborious, candidate-based methods.
Here, we report a detailed protocol to perform a high-throughput, proteome-wide unbiased identification of RNA-binding proteins and their RNA-binding regions. The methodology relies on the incorporation of a photoreactive uridine analog in the cellular RNA, followed by UV-mediated protein-RNA crosslinking, and mass spectrometry analyses to reveal RNA-crosslinked peptides within the proteome. Although we describe the procedure for mouse embryonic stem cells, the protocol should be easily adapted to a variety of cultured cells.

We describe a protocol to identify RNA-binding proteins and map their RNA-binding regions in live cells using UV-mediated photocrosslinking and mass spectrometry.

Noncoding RNAs play important roles in several nuclear processes, including regulating gene expression, chromatin structure, and DNA repair. In most ...

Structural Characterization of Mannan Cell Wall Polysaccharides in Plants Using PACE

Plant cell wall polysaccharides are notoriously difficult to analyze, and most methods require expensive equipment, skilled operators, and large amounts of purified material. Here, we describe a simple method for gaining detailed polysaccharide structural information, including resolution of structural isomers. For polysaccharide analysis by gel electrophoresis (PACE), plant cell wall material is hydrolyzed with glycosyl hydrolases specific to the polysaccharide of interest (e.g., mannanases for mannan). Large format polyacrylamide gels are then used to separate the released oligosaccharides, which have been fluorescently labeled. Gels can be visualized with a modified gel imaging system (see Table of Materials). The resulting oligosaccharide fingerprint can either be compared qualitatively or, with replication, quantitatively. Linkage and branching information can be established using additional glycosyl hydrolases (e.g., mannosidases and galactosidases). Whilst this protocol describes a method for analyzing glucomannan structure, it can be applied to any polysaccharide for which characterized glycosyl hydrolases exist. Alternatively, it can be used to characterize novel glycosyl hydrolases using defined polysaccharide substrates.

A protocol for the structural analysis of polysaccharides by gel electrophoresis (PACE), using mannan as an example, is described.

Plant cell wall polysaccharides are notoriously difficult to analyze, and most methods require expensive equipment, skilled operators, and large amounts ...

Using Three-color Single-molecule FRET to Study the Correlation of Protein Interactions

Single-molecule F&#246;rster resonance energy transfer (smFRET) has become a widely used biophysical technique to study the dynamics of biomolecules. For many molecular machines in a cell proteins have to act together&#160;with interaction partners in a functional cycle to fulfill their task. The extension of two-color to multi-color smFRET makes it possible to simultaneously probe more than one interaction or conformational change. This not only adds a new dimension to smFRET experiments but it also offers the unique possibility to directly study the sequence of events and to detect correlated interactions when using an immobilized sample and a total internal reflection fluorescence microscope (TIRFM). Therefore, multi-color smFRET is a versatile tool for studying biomolecular complexes in a quantitative manner and in a previously unachievable detail.
Here, we demonstrate how to overcome the special challenges of multi-color smFRET experiments on proteins. We present detailed protocols for obtaining the data and for extracting kinetic information. This includes trace selection criteria, state separation, and the recovery of state trajectories from the noisy data using a 3D ensemble Hidden Markov Model (HMM). Compared to other methods, the kinetic information is not recovered from dwell time histograms but directly from the HMM. The maximum likelihood framework allows us to critically evaluate the kinetic model and to provide meaningful uncertainties for the rates.
By applying our method to the heat shock protein 90 (Hsp90), we are able to disentangle the nucleotide binding and the global conformational changes of the protein. This allows us to directly observe the cooperativity between the two nucleotide binding pockets of the Hsp90 dimer.

Here, we present a protocol to obtain three-color smFRET data and its analysis with a 3D ensemble Hidden Markov Model. With this approach, scientists can extract kinetic information from complex protein systems, including cooperativity or correlated interactions.

Single-molecule F&#246;rster resonance energy transfer (smFRET) has become a widely used biophysical technique to study the dynamics of biomolecules. For ...

Dissipative Microgravimetry to Study the Binding Dynamics of the Phospholipid Binding Protein Annexin A2 to Solid-supported Lipid Bilayers Using a Quartz Resonator

The dissipative quartz crystal microbalance technique is a simple and label-free approach to measure simultaneously the mass uptake and viscoelastic properties of the absorbed/immobilized mass on sensor surfaces, allowing the measurements of the interaction of proteins with solid-supported surfaces, such as lipid bilayers, in real-time and with a high sensitivity. Annexins are a highly conserved group of phospholipid-binding proteins that interact reversibly with the negatively charged headgroups via the coordination of calcium ions. Here, we describe a protocol that was employed to quantitatively analyze the binding of annexin A2 (AnxA2) to planar lipid bilayers prepared on the surface of a quartz sensor. This protocol is optimized to obtain robust and reproducible data and includes a detailed step-by-step description. The method can be applied to other membrane-binding proteins and bilayer compositions.

Here, we present an experimental protocol that can be employed to determine the binding affinities and mode of interaction of label-free phospholipid-binding protein annexin A2 with immobilized solid-supported bilayers (SLB) by simultaneously measuring the mass uptake and the viscoelastic properties of the protein annexin A2.

The dissipative quartz crystal microbalance technique is a simple and label-free approach to measure simultaneously the mass uptake and viscoelastic ...

Modifying Baculovirus Expression Vectors to Produce Secreted Plant Proteins in Insect Cells

It has been a challenge for scientists to express recombinant secretory eukaryotic proteins for structural and biochemical studies. The baculovirus-mediated insect cell expression system is one of the systems used to express recombinant eukaryotic secretory proteins with some post-translational modifications. The secretory proteins need to be routed through the secretory pathways for protein glycosylation, disulfide bonds formation, and other post-translational modifications. To improve the existing insect cell expression of secretory plant proteins, a baculovirus expression vector is modified by the addition of either a GP67 or a hemolin signal peptide sequence between the promoter and multiple-cloning sites. This newly designed modified vector system successfully produced a high yield of soluble recombinant secreted plant receptor proteins of Arabidopsis thaliana. Two of the expressed plant proteins, the extracellular domains of Arabidopsis TDR and PRK3 plasma membrane receptors, were crystallized for X-ray crystallographic studies. The modified vector system is an improved tool that can potentially be used for the expression of recombinant secretory proteins in the animal kingdom as well.

Here, we present the protocols for utilizing the insect cell and baculovirus protein expression system to produce large quantities of plant secreted proteins for protein crystallization. A baculovirus expression vector has been modified with either GP67 or insect hemolin signal peptide for plant protein secretion expression in insect cells.

It has been a challenge for scientists to express recombinant secretory eukaryotic proteins for structural and biochemical studies. The ...

Structural Studies of Macromolecules in Solution using Small Angle X-Ray Scattering

Protein-protein interactions involving proteins with multiple globular domains present technical challenges for determining how such complexes form and how the domains are oriented/positioned. Here, a protocol with the potential for elucidating which specific domains mediate interactions in multicomponent system through ab initio modeling is described. A method for calculating solution structures of macromolecules and their assemblies is provided that involves integrating data from small angle X-ray scattering (SAXS), chromatography, and atomic resolution structures together in a hybrid approach. A specific example is that of the complex of full-length nidogen-1, which assembles extracellular matrix proteins and forms an extended, curved nanostructure. One of its globular domains attaches to laminin &#947;-1, which structures the basement membrane. This provides a basis for determining accurate structures of flexible multidomain protein complexes and is enabled by synchrotron sources coupled with automation robotics and size exclusion chromatography systems. This combination allows rapid analysis in which multiple oligomeric states are separated just prior to SAXS data collection. The analysis yields information on the radius of gyration, particle dimension, molecular shape and interdomain pairing. The protocol for generating 3D models of complexes by fitting high-resolution structures of the component proteins is also given.

Here, we present how Small Angle X-Ray Scattering (SAXS) can be utilized to obtain information on low-resolution envelopes representing the macromolecular structures. When used in conjunction with high-resolution structural techniques such as X-Ray Crystallography and Nuclear Magnetic Resonance, SAXS can provide detailed insights into multidomain proteins and macromolecular complexes in-solution.

Protein-protein interactions involving proteins with multiple globular domains present technical challenges for determining how such complexes form and ...

Analysis of Protein Folding, Transport, and Degradation in Living Cells by Radioactive Pulse Chase

Radioactive pulse-chase labeling is a powerful tool for studying the conformational maturation, the transport to their functional cellular location, and the degradation of target proteins in live cells. By using short (pulse) radiolabeling times (&lt;30 min) and tightly controlled chase times, it is possible to label only a small fraction of the total protein pool and follow its folding. When combined with nonreducing/reducing SDS-polyacrylamide gel electrophoresis (SDS-PAGE) and immunoprecipitation with (conformation-specific) antibodies, folding processes can be examined in great detail. This system has been used to analyze the folding of proteins with a huge variation in properties such as soluble proteins, single and multi-pass transmembrane proteins, heavily N- and O-glycosylated proteins, and proteins with and without extensive disulfide bonding. Pulse-chase methods are the basis of kinetic studies into a range of additional features, including co- and posttranslational modifications, oligomerization, and polymerization, essentially allowing the analysis of a protein from birth to death. Pulse-chase studies on protein folding are complementary with other biochemical and biophysical methods for studying proteins in vitro by providing increased temporal resolution and physiological information. The methods as described within this paper are adapted easily to study the folding of almost any protein that can be expressed in mammalian or insect-cell systems.

Here we describe a protocol for a general pulse-chase method that allows the kinetic analysis of folding, transport, and degradation of proteins to be followed in live cells.

Radioactive pulse-chase labeling is a powerful tool for studying the conformational maturation, the transport to their functional cellular location, and ...

Estimation of Structural Sensitivity of Intrinsically Disordered Regions in Response to Hyperosmotic Stress in Living Cells Using FRET

Summary

Explore More Videos

Chapters in this video

Structural Information from Single-molecule FRET Experiments Using the Fast Nano-positioning System

Using Scaffold Liposomes to Reconstitute Lipid-proximal Protein-protein Interactions In Vitro

Nuclear Magnetic Resonance Spectroscopy for the Identification of Multiple Phosphorylations of Intrinsically Disordered Proteins

Sample Preparation for Mass Spectrometry-based Identification of RNA-binding Regions

Structural Characterization of Mannan Cell Wall Polysaccharides in Plants Using PACE

Using Three-color Single-molecule FRET to Study the Correlation of Protein Interactions

Dissipative Microgravimetry to Study the Binding Dynamics of the Phospholipid Binding Protein Annexin A2 to Solid-supported Lipid Bilayers Using a Quartz Resonator

Modifying Baculovirus Expression Vectors to Produce Secreted Plant Proteins in Insect Cells

Structural Studies of Macromolecules in Solution using Small Angle X-Ray Scattering

Analysis of Protein Folding, Transport, and Degradation in Living Cells by Radioactive Pulse Chase