One of the most important regulatory small molecules in plants is indole-3-acetic acid, also known as auxin. Its dynamic redistribution has an essential role in almost every aspect of plant life, ranging from cell shape and division to organogenesis and responses to light and gravity1,2. So far, it has not been possible to directly determine the spatial and temporal distribution of auxin at a cellular resolution. Instead it is inferred from the visualization of irreversible processes that involve the endogenous auxin-response machinery3,4,5,6,7; however, such a system cannot detect transient changes. Here we report a genetically encoded biosensor for the quantitative in vivo visualization of auxin distribution. The sensor is based on the Escherichia coli tryptophan repressor8, the binding pocket of which is engineered to be specific to auxin. Coupling of the auxin-binding moiety with selected fluorescent proteins enables the use of a fluorescence resonance energy transfer signal as a readout. Unlike previous systems, this sensor enables direct monitoring of the rapid uptake and clearance of auxin by individual cells and within cell compartments in planta. By responding to the graded spatial distribution along the root axis and its perturbation by transport inhibitors—as well as the rapid and reversible redistribution of endogenous auxin in response to changes in gravity vectors—our sensor enables real-time monitoring of auxin concentrations at a (sub)cellular resolution and their spatial and temporal changes during the lifespan of a plant.
The tryptophan-derived metabolite indole-3-acetic acid (IAA) has an important role in plants, triggering a multitude of developmental processes and responses to environmental cues1,2. Much progress has been made towards a mechanistic understanding of the nuclear events that transform auxin perception into transcriptional responses9,10,11. Other studies have investigated the basic machinery involved in the polar and non-vectorial release of auxin from the cell—which occurs through the action of PINFORMED efflux transporters and ABCB transporters— within a tissue context, and have resulted in computer models of how canalized auxin flow mediates developmental or physiological processes12,13,14. By contrast, owing to technical limitations (reviewed in ref. 15), very little is known about the actual distribution of auxin in tissues at single-cell resolution. At present, plant biologists can use only proxies to visualize auxin distribution, such as the auxin-dependent expression of reporter genes (for example, using the systems DR5::GUS3; DR5::ER-GFP4 and DR5::NLS-3xGFP5). However, this indirect approach is characterized by latencies and can be affected by modulation of the auxin signalling machinery. More recently, IAA levels have been inferred from auxin-dependent degradation—and thus signal reduction—of fluorescent proteins linked to domain II of an IAA inhibitory protein (for example, DII-VENUS6 and R2D27). A limitation of these approaches is their irreversibility, which precludes the visualization of transient changes in auxin levels.
The ideal sensor for the visualization of auxin dynamics in planta should have the following features: first, physical interaction of the sensor with auxin should elicit a fluorescent signal in a reversible manner, so that changes in auxin concentration can be monitored; second, the sensitivity of the sensor should be sufficiently high to image the dynamic auxin distribution over time; third, the sensor should be targetable to different subcellular compartments—locations that are out of reach for the conventional proxies, which rely on gene expression or protein degradation; and fourth, the sensor should not contain components that are involved in plant metabolism or regulation, such that both interference with auxin responses and regulation of the sensor by the plant are avoided.
With these boundary conditions in mind, we developed a genetically encoded, fully reversible biosensor for in vivo imaging of auxin gradients with high spatial and temporal resolution, starting from the bacterial tryptophan repressor (TrpR). IAA resembles tryptophan: both contain an indole ring, the 3-position of which is connected to an amino acid moiety in TRP and a carboxyl group in IAA (Fig. 1a). The dimeric TrpR undergoes a conformational change upon binding TRP16,17, and fluorescent proteins fused to TrpR can relay this change, generating a fluorescence resonance energy transfer (FRET) signal as a convenient readout for in vivo measurements18 (Fig. 1b). Furthermore, TrpR exhibits low affinity towards IAA8. This makes TrpR an ideal starting point for developing an auxin-specific, genetically encoded FRET biosensor19. Our design efforts were aimed at improving the affinity and specificity of IAA binding, while abolishing TRP binding. We assumed a comparable binding mode for the indole ring of both TRP and IAA, and focused our design around the TrpR residues in the vicinity of the amino group of TRP (Fig. 1c), aiming to improve the specificity for the carboxyl group of IAA. This selection was later expanded to include adjacent residues. Altogether, 2,000 variants were generated in successive rounds of mutagenesis and were screened for an increase in FRET signal upon the addition of IAA (Fig. 1d, Extended Data Fig. 1). Improved variants were checked for ligand specificity using a library of substances that are similar to IAA and are reportedly present in Arabidopsis (Extended Data Table 1). To confirm improvements in binding affinity, selected TrpR variants were analysed by isothermal titration calorimetry (Extended Data Table 2a). Furthermore, the structures of several variants were elucidated by X-ray crystallography, to guide mutagenesis experiments (Extended Data Table 2b, Supplementary Table 1a–h).
Our structural analysis showed that, when binding to TrpR, IAA is flipped by 180° compared with TRP (Fig. 2a), with the carboxyl group of IAA facing the opening of the TrpR binding pocket (Fig. 2b). TRP is anchored by interactions with the surrounding protein residues, whereas IAA binding shows no such stabilization, which is reflected in the poor binding affinity of this interaction (Extended Data Table 2a). In engineering the auxin sensor, we identified variants that stabilize and favour this IAA-binding mode. Primarily, a serine-to-tyrosine mutation at position 88 (S88Y) was found to entirely block TRP binding owing to the bulky side chain of Y88, while simultaneously favouring IAA binding through interaction of the carboxyl group of IAA with the guanidino group of R84 and the hydroxyl group of Y88 (Fig. 2c). The affinity for IAA was improved further by optimizing hydrophobic interactions of its indole ring with the TrpR binding pocket; to this end, the mutations T44L and T81M were incorporated in the final sensor design (Fig. 2d). During the engineering process, we also monitored the binding of indole-3 acetonitrile (IAN)—which could potentially compete with IAA—to TrpR (Extended Data Table 2a). The binding modes of IAN and IAA are markedly similar (Extended Data Fig. 2a, b); however, mutations such as N87G exert discriminating effects through small changes in the positioning of Y88 (Extended Data Fig. 2c). Finally, we identified mutations that have no favourable effect on IAA affinity but improve the FRET readout—probably through changes in the packing, and therefore the orientation, of the attached fluorescent proteins (Extended Data Fig. 2d). We then optimized the fluorophores and the linker combinations (Extended Data Fig. 3) to yield our final sensor, which we term ‘AuxSen’, with the composition mNeonGreen–TrpR–Aquamarine–TrpR, in which TrpR is TrpR(M42F/T44L/T81M/N87G/S88Y) (Figs. 1d, 2d).
In vitro, the FRET ratio of AuxSen changed by a factor of three upon treatment with 50 μM IAA, which is within the range of cellular auxin concentrations20. The signal was stable at cytosolic pH, and in the presence of reducing or oxidizing environments and all tested salt ions (Extended Data Fig. 4). The specificity of AuxSen for IAA was assessed using other indole derivatives. Among these, AuxSen showed the highest affinity for IAA; although a response was observed for other compounds, their binding affinities were reduced by around one order of magnitude (Extended Data Fig. 5). Of these indole derivatives, only IAN is present in substantial amount in plants (Extended Data Table 1). However, roots show a growth response to treatment with IAN, and modelling suggests that the IAA receptor SCFTIR1 could bind IAN21. Thus, IAN is probably sequestered and is therefore unlikely to interfere with auxin sensing in the plant.
As a first step to confirm the functionality of AuxSen in vivo, we expressed a nuclear-localized version of the sensor transiently from the viral 35S promoter in cell-suspension protoplasts22, and quantified the FRET response by flow cytometry. The FRET ratio increased with the auxin concentration in the medium over four orders of magnitude, starting at 3 μM IAA (Fig. 3a, b, Extended Data Figs. 6, 7), with the baseline FRET signal thought to reflect the endogenous level of auxin in the protoplast population. The sensitivity of the sensor could therefore be sufficient to report endogenous auxin levels.
We generated approximately 250 transgenic Arabidopsis lines bearing a dexamethasone-inducible expression system (pBay-bar-pRPS5a-mGAL4-VP16-GR_UAS_NLS_AuxSen) integrated as a single transgene, and selected 10 lines expressing the sensor stably in the fourth generation. The strong, ubiquitously active promoter RPS5A drives expression of the yeast transcription factor Gal4p, the nuclear uptake of which is induced by dexamethasone, and the binding of Gal4p to the UAS promoter results in the expression of the nuclear-localized auxin sensor. Strongly expressing lines were identified by mNeonGreen fluorescence in the root tips after dexamethasone induction overnight. To examine the response of AuxSen to auxin in planta, we treated seedlings with 10 μM IAA and recorded the FRET signal over time (Fig. 3c–f). After 10 min, the FRET signal in root nuclei had reached a maximum, and then remained constant for another 50 min; by contrast, treatment with the solvent DMSO did not induce any response (Fig. 3c, d). To reveal the speed of nuclear auxin accumulation, we measured the FRET signal over shorter time intervals. The maximum signal was reached within 2 min, with more than 80% achieved after only 1 min (Fig. 3e, f). The uptake of auxin from the extracellular space therefore seems to be highly efficient. We then investigated the reversibility of nuclear accumulation by washing out IAA. After 10 min of incubation of seedlings in 10 μM IAA, which gave the maximum FRET ratio, the medium was changed to DMSO (Fig. 3g, h). The FRET ratio gradually decreased, almost reaching the pre-incubation value 30 min later, which suggests slow IAA efflux from the cells (Fig. 3g, h). We repeated the experiment but extended the IAA incubation time to 1 h. This accelerated IAA efflux such that the FRET ratio decreased to its pre-incubation level within 10 min of IAA withdrawal (Fig. 3g, h). This increased efflux of IAA correlated with two- to threefold higher expression levels of PIN efflux carriers after 1 h compared to 10 min of IAA incubation (Extended Data Fig. 8). In conclusion, this FRET-based sensor can report the dynamics of transient auxin accumulation. Although traditional reporter systems can detect the response to auxin uptake6, the irreversibility of reporter translation or degradation obscures the transient nature of the auxin response. Our data suggest that IAA uptake is a constitutive, fast process, whereas the efflux from the cell occurs on demand, as if auxin regulates its own export.
To explore whether auxin might accumulate in other subcellular compartments—those that cannot be accessed by reporters that are based on gene expression or protein degradation—we targeted AuxSen to the lumen of the endoplasmic reticulum (ER). The localization of PIN and PIN-LIKE putative auxin transporters in the ER membrane has led to speculation that auxin accumulation in the ER could be an ancient mechanism of auxin homeostasis23. Incubating seedlings in 100 μM IAA for 15 min led to a strong increase in the FRET ratio compared with the DMSO control, suggesting that IAA is transported into the ER (Fig. 3i, j). Different cells within the same seedling root displayed different levels of AuxSen accumulation in the ER (Fig. 3i). Nonetheless, the change in FRET ratio upon exposure to IAA did not differ substantially between cells expressing higher or lower levels of AuxSen (Fig. 3j). In conclusion, this FRET-based auxin sensor can faithfully report auxin concentrations from a subcellular compartment such as the ER, which is inaccessible to traditional auxin-response reporters.
The spatial distribution of endogenous auxin in the seedling root has been inferred from the steady-state expression levels of auxin-response reporters such as pDR5:GFP or p35S:DII-VENUS, which display a pronounced maximum at the quiescent centre of the root meristem near the root tip6. Consistent with this, the FRET ratio of our auxin sensor steadily increased towards the root tip, although there was no prominent maximum (Fig. 4a, b). To assess the contribution of transport to the steady-state distribution of auxin, we incubated the seedlings in brefeldin A, which impairs auxin transport by inhibiting the polar recycling of the auxin efflux transporter PIN124. FRET ratios were increased in the tip of treated roots compared to untreated controls (Fig. 4a, b). This increase presumably resulted from ongoing IAA synthesis in the root tip while efflux was impaired, which is consistent with mass spectrometry analysis of IAA biosynthesis in cell-sorted GFP-expressing lines20 and with the expression of auxin-biosynthesis genes in the root tip25. We conclude that AuxSen reports the perturbation of endogenous auxin distribution, which highlights its specificity for the detection of auxin.
The redirection of root growth in response to changes in orientation of the gravity vector is a prime example of rapid auxin signalling, which involves redistribution of endogenous auxin within the root tip26. Relocalization of the auxin efflux transporter PIN3 from the (former) basal to the (former) lateral plasma membrane has been detected 2 min after turning the root to a horizontal position27. However, to our knowledge, no concomitant change in auxin distribution has been reported. The earliest change that has been detected, using the auxin-responsive degradation reporter DII-VENUS, was a reduction in fluorescence in the new lower side 30 min after the onset of gravity stimulation28. We equilibrated seedling roots mounted in a near-vertical position for 1 h, then changed their orientation by 135° and monitored the nuclear FRET ratios over time (Fig. 4c, d). Within 1 min, there was a distinct increase in FRET ratio on the new lower side of the root tip, corresponding to more than 80% of the maximum value reached after 5 min. We then returned the roots to the near-vertical position after 30 min, and detected substantial recovery of the pre-stimulation distribution of FRET signals within 1 min (Fig. 4c, d). Gravistimulation therefore elicits a fast and reversible response of the auxin transport system in the root tip. In conclusion, this auxin sensor reports the rapid and reversible redistribution of endogenous auxin accumulation.
Our design approach has yielded a new sensor, AuxSen, for the pervasive plant signalling molecule auxin. Starting from a tryptophan sensor, we optimized the affinity and specificity for the binding of IAA, and improved the signal intensity through choice of the FRET pair and optimization of the linkers. Our results provide a proof-of-principle that this detection system can visualize the dynamic redistribution of auxin as well as subcellular pools of auxin, which cannot be achieved with the auxin reporters that are currently in use. An example of insights into auxin dynamics that have been made possible by the resolving power of AuxSen is the contrast between the efficient uptake and the slower, conditional efflux of auxin. Furthermore, AuxSen enables changes in auxin distribution to be distinguished from changes in auxin response, which is a prerequisite for investigating the complex regulatory network that underlies the biological effects of this major signalling molecule in plant growth and development.
No statistical methods were used to predetermine sample size. The experiments were not randomized and the investigators were not blinded to allocation during experiments and outcome assessment.
Cloning of in-vitro auxin sensors
The TrpR sensors Trp-CTY and Trp-CTYT were gifts from W. Frommer (Addgene plasmids 13533 and 13534). The fluorophores tested were also donated: Aquamarine by F. Merola (Addgene plasmid 42888), Clover and mRuby2 by K. Beam (Addgene plasmid 49089), mKO1 by K. Thorn (Addgene plasmid 44642) and mCherry by M. Bayer29. eGFP was amplified from pGIIK NLS:3xEGFP30. mNeonGreen, mWasabi and mTFP1 were purchased from Allele Biotechnology and Pharmaceuticals, mKate2 and TagRFP were from Evrogen.
For the initial screening, we first used the Trp-CTY sensor and mutated the residues T44 and S88 individually to all possible amino acids. To this end, we generated primers with 15–16 bp overlaps around the exchanged amino acid codons. We first mutated the amino acids sequence randomly with a degenerate primer and screened 96 clones. Variants not found were then generated by targeted mutagenesis. For example, to generate all T44 variants we first used the primers CCTGATGCTGnnnCCAGATGAGCGCG and CGCGCTCATCTGGnnnCAGCATCAGG, to generate the missing T44C variant we then used the primers CCTGATGCTGtgtCCAGATGAGCGCG and CGCGCTCATCTGGacaCAGCATCAGG. The most promising candidates were introduced by targeted mutagenesis into Trp-CTYT and TrpR without fluorescent proteins, which were analysed by isothermal titration calorimetry (ITC) and structural studies. Trp-CTYT with mutations T44L and S88Y was generated in two steps: we first used the primers CCTGATGCTGctaCCAGATGAGCGCG and CGCGCTCATCTGGtagCAGCATCAGG to generate Trp-CTYT with T44L and then GATTACGCGTGGATCTAACtac-CTGAAAGCCGCGCCC and GGGCGCGGCTTTCAGgtaGTTAGATCCACGCGTAATC to generate Trp-CTYL with the mutations T44L and S88Y. To produce the recombinant proteins, we cloned the TrpR domain into the pET21 expression vector and generated the variants by targeted mutagenesis. This procedure was repeated with the most promising variants after each round. The primer sequences are available upon request.
The final variant was then codon-optimized for Arabidopsis and synthesized by Thermo Fisher Scientific GENEART. To allow an easy exchange of the fluorophores we added restriction enzyme sites at the ends: BamH1 and XhoI around the first fluorophore and ApaI and HindIII around the second. All fluorescent proteins were tested in the fluorophore I–TrpR–fluorophore II–TrpR configuration. Having identified Aquamarine and mNeonGreen as the optimal pair, we introduced all final binding-pocket variants into the backbone by site-directed mutagenesis.
Ligands used for screening and testing
IAA, TRP, IAN, indole-3-carboxaldehyde, indole, indole-3-acetyl alanine, indole-3-acetyl aspartic acid, indole-3-acetamide, indole-3-ethanol, l-kynurenine, 2-oxindole-3-acetic acid, phenylalanine, picloram, tryptamine, (NH4)2SO4, CaCl2, DTT, H2O2, NH4NO3, KNO3 and yucasin were purchased from Sigma-Aldrich; 4-hydroxyindole-3-carbaldehyde and 5-hydroxyindole-3-carboxylic acid from Santa Cruz Biotechnology; 1-naphthaleneacetic acid, KCl and DMSO from Carl-Roth; 2,4-dichlorophenoxyacetic acid (2,4-D) from Alfa Aesar; indole-3-acetyl glucose from TRC; indole-3-butyric acid from Serva; NaCl from Merck; NPA from Supelco; and BFA from Thermo Fisher Scientific.
Trp-CTY variants were generated by site-directed mutagenesis with degenerate or specific oligonucleotides purchased from Sigma-Aldrich. Amplification was carried out using Pfu polymerase (Thermo Fisher Scientific).
More than one thousand oligonucleotides were used; the sequences and resulting vector maps are available upon request. Each variant was sequenced and screened in crude extract of sonicated bacteria for IAA binding; promising candidates were confirmed as purified proteins. The linkers were generated by site-directed mutagenesis, including linkers with 15–16 bp overlap and 3–9 degenerated nucleotides in the middle. To generate linkers shorter than the original ones, parts were deleted, whereas for longer linkers a fixed sequence was inserted into the middle to reduce the risk of generating stop codons by having too many degenerate nucleotides in the sequence.
Protein expression and purification for screening
For protein expression, bacteria were grown in the dark on plates with LB-agar supplemented with ampicillin for 3 days at room temperature. To measure crude extracts, we resuspended the bacteria in 20 mM MOPS pH 7.2, sonicated the suspension with an MS 73 probe (Bandelin) and centrifuged the sample with a tabletop centrifuge (Eppendorf). Protein extraction was performed with His Spin trap columns according to the manufacturer’s instructions (GE Healthcare). We resuspended the bacteria of one Petri dish in 2 ml binding buffer and sonicated with a MS 73 probe. Buffer exchange was performed with illustra NAP-25 columns (GE Healthcare). All measurements were performed in 20 mM MOPS (Sigma-Aldrich) with an Infinite F200 plate reader (Tecan).
Ligands used for crystallization and ITC
IAA, IAN and TRP used for crystallization and ITC were dissolved in 50 mM Tris/300 mM NaCl pH 8 buffer containing 1% DMSO if necessary.
Protein purification for crystallography and ITC
After subcloning to pET21b(+), wild-type TrpR and all variants were expressed in E. coli BL21(DE3) and purified with a NiIMAC column and a subsequent Superdex-S75 gel-filtration column. All purification steps and measurements were based on the above 50 mM Tris/300 mM NaCl pH 8 buffer.
Crystallization, data collection and processing
Crystals of wild-type TrpR and variants with different ligands were obtained by standard vapour diffusion in sitting drop plates. The crystals were cryoprotected if needed and flash-cooled in liquid nitrogen. Data for single crystals were collected at the synchrotron beamline PXII (Swiss Light Source) at 100 K and 0.5 degree images were recorded on a Pilatus 6 M detector. Only variant TrpR(M42F/T44L/T81M/N87G/S88Y)–IAA was recorded at MX Beamlines BL14.1 at BESSY II (Helmholtz-Zentrum Berlin für Materialien und Energie). Data were indexed, integrated and scaled with the program XDS and converted with XDSCONV31. Molecular replacement was performed with Phenix using the coordinates of wild-type TrpR (PDB ID: 1WRP32 or 1TRO33) as search model. Model building was performed using the program Coot34, and refinement was performed using Phenix35. Details on crystallization conditions, data and refinement statistics for all structures are summarized in Extended Data Table 2b and Supplementary Table 1.
ITC was performed using a VP-ITC (MicroCal). The protein concentration was adjusted to 74 μM and 730 μM ligand solutions were prepared using the above buffer containing 1% DMSO. Measurements were performed at 20 °C with a stirring speed of 300 rpm, reference power 15 μcal s−1 and spacing of 300 s between injections. The data were analysed using the MicroCal program. Binding data were derived from sigmoidal fits based on a one-site binding model from two measurements for each variant. Heat-of-dilution baselines for the ligands alone were subtracted from the experimental data as previously described36. The pH dependence of IAA binding to the variant TrpR(M42F/T44L/T81M/N87G/S88Y) (AuxSen) was measured on a NanoITC LV device with a stir rate of 300 rpm, 15 injections with 2 μl and 300 s spacing between injections. The 170 μl cell was overfilled with 400 μl protein to ensure air-free filling. The protein was added at a concentration of 100 μM and the ligand IAA at 1 mM at 20 °C. For each pH the data were recorded in the respective buffer: (i) 50 mM Tris pH 8.5, 300 mM NaCl; (ii) 50 mM Tris pH 8.0, 300 mM NaCl; (iii) 50 mM Tris pH 7.5, 300 mM NaCl; (iv) 50 mM Tris pH 7.0, 300 mM NaCl; (v) 50 mM MES pH 6.5, 300 mM NaCl; (vi) 50 mM MES pH 6.0, 300 mM NaCl; (vii) 50 mM MES pH 5.5, 300 mM NaCl; (viii) 50 mM citrate buffer pH 5.0, 300 mM NaCl; and (ix) 50 mM citrate buffer pH 4.5, 300 mM NaCl.
Test of different FRET pairs
We tested pairs of Aquamarine, mCerulean3, mTFP1 and mTurquoise2 with Clover, Ypet and mNeonGreen; Aquamarine was additionally tested with eGFP and mWasabi, and mTFP1 with TagRFP. Furthermore, we tested mNeonGreen, Clover and Ypet with TagRFP and mRuby2. mKO1 was tested with mCherry, mKate2, mNeonGreen and mWasabi. TagRFP was also tested with mTFP1, mWasabi, mKate2 and mCherry.
Constructs for in-vivo AuxSen experiments
For protoplast expression, we cloned the final version of the sensor into pJIT6022 (pJIT60-2xp35S:NLS:AuxSen).
For expression in transgenic plants, we cloned the in-vitro optimized AuxSen in constructs for conditional two-component expression, using the pBay-bar vector (a gift from M. Bayer37). pRPS5a-mGAL4-VP16-GR-UAS_NLS was amplified from a pGII plasmid and inserted into pBay-bar digested with KpnI and BamHI with Gibson Assembly (In-Fusion Cloning, Takara Bio Europe SAS) according to the manufacturer´s instructions. In a second step, AuxSen and ocs terminator were inserted into pBay-bar pRPS5a-mGAL4-VP16-GR_UAS_NLS digested with BamHI. To obtain the individual spectra, we replaced AuxSen by mNeonGreen or Aquamarine. These constructs were used for transforming plants and as a template for the unmix matrix in Fiji. To generate the ER-localized auxin sensor SP:AuxSen:HDEL, we removed the NLS from the nuclear AuxSen construct and inserted the signal peptide of an Arabidopsis vacuolar basic chitinase and the HDEL ER retention sequence38 in frame with the coding sequence N-terminally and C-terminally, respectively.
Flow cytometry of protoplasts transiently expressing AuxSen
Protoplasts were prepared from suspension cell cultures and transfected as previously described39, using 12-ml PP tubes and 12 μg of construct pJIT60-2xp35S:NLS:AuxSen per 120 μl of protoplasts (3.5 × 106 per ml) per transfection. On the next day, transfected protoplasts were pooled, filtered through 100-μm nylon mesh and split into 200-μl aliquots. Each IAA stock (in DMSO) was added 1:100 with a timing offset to account for the 5-min measurement cycle, ensuring a 1-h treatment for each sample, performed in triplicate. Cytometric analysis was set up on a Beckman Coulter MoFlo XDP (100 μm CytoNozzle, 30.5/30.0 psi, PBS sheath) to excite mNeonGreen at 488 nm (70 mW, elliptical focus) and capture peak FL1 (534/30) and shoulder FL2 (585/29) emission; Aquamarine at 405 nm excitation (100 mW, spherical focus) and capture peak FL9 (465/30) and shoulder FL10 (529/28) emission. Data were collected and processed using Summit 5.5 (Beckman Coulter). The main light-scattering gate was determined by identifying the population expressing the greatest amount of reporter. The FRET response was the ratio mean of FL10/FL9, with the auxin response moving towards FL10, directly calculated in Summit 5.5. Representative plots were drawn with FCS Express v.6.06.0033 (deNovo).
Plant material and growth conditions
Wild-type Arabidopsis thaliana (accession Col-0) plants were used for transformation. Plants were grown on soil at 24 °C, 65% relative humidity under long-day conditions (16-h illumination and 8-h dark period). Seeds were surface-sterilized, stratified for 2 days at 4 °C and grown on half-strength Murashige and Skoog agar plates containing 1% sucrose (0.5MS + S) (Serva). After 1 week plants were transferred to soil.
For imaging, 4-day-old seedlings were transferred to 0.5MS+S 25 μM DEX agar plates, and 16 h later to microscope slides on which they were incubated in 0.5MS+S + IAA or DMSO (control) at the specified concentrations and for the indicated periods of time. To preserve field-of-view and optimal buffer exchange we fixed the cover slip and root with double-sided adhesive tape (Tesa, type 05338, Beiersdorf). To exchange the buffer, we completely emptied the slide on a paper tissue and refilled from the side with the pipette. For BFA treatment, seedlings were transferred to 0.5MS+S 25 μM DEX plates containing either 10 μM BFA or 0.1% (v/v) DMSO (control), and mounted on microscope slides 10 h later.
The imaging of seedling roots was performed with an LSM780 confocal laser scanning microscope, running ZEN 2.3 black SP1 as acquisition software (Zeiss) and using a Zeiss LD C-Apochromat 40×/1,1 W Korr for all experiments except the gravitropism experiments, which were recorded with a Zeiss Plan-Apochromat 20×/0.8. Spectral imaging was performed using the QUASAR detection unit on the same system: Aquamarine was excited for FRET ratio measurement at 405 nm using 5 fluorescent channels (419–455 nm, 454–491 nm, 490–526 nm, 525–562 nm and 561–598 nm); subsequently, mNeonGreen was imaged for segmentation of the regions of interest with excitation at 488 nm and detection of 3 fluorescent channels (490–526 nm, 525–562 nm and 561–598 nm). Gravitropism imaging requiring control over the direction of gravity was performed with a custom-made horizontal imaging kit that can be equipped on most inverted microscope stands for wide-field and confocal imaging. The kit consists of two pieces: a holder for the objective with a mirror for changing the direction of the optical axis of the system from a vertical direction to a horizontal direction (components from Thorlabs). The second piece is a rotatable, vertical sample holder that can be mounted into a standard multiwell plate holder (components from Fischertechnik).
We used spectral FRET40 to be able to control for influences from sources of autofluorescence, which can be abundant in plant tissues41. Spectral FRET therefore also has the advantage that the method can be adapted by adjusting the number of acquisition channels if other sources of autofluorescence are present in different plant tissues.
All analyses were performed using a current version of Fiji42. First, signals generated were linearly unmixed43 using J. Walter’s spectral unmixing plugin (https://imagej.nih.gov/ij/plugins/spectral-unmixing.html). The unmixing matrix was generated with mNeonGreen, and Aquamarine as fluorophore controls and a wild-type Col-0 control for background autofluorescence. After this, the images were manually thresholded on all channels to remove unspecific signals and saturated areas, regions of interest (ROIs) for the cell nuclei were automatically generated based on the 488 nm/490–526 nm-channel data using an adaptive threshold plugin (by Q. Tseng, https://sites.google.com/site/qingzongtseng/adaptivethreshold) and the ‘Watershed’ and ‘Analyze Particles’ functions of ImageJ. We analysed all pixels of the image only for the ER. The FRET ratio was calculated by spectral unmixing of the channels using ‘Spectral Unmix’ version 1.3 (by J. Walter, https://imagej.nih.gov/ij/plugins/spectral-unmixing.html) and a precomputed unmixing matrix (see above) yielding the Aquamarine and mNeonGreen emission for division. Unmixed ROIs were colour-coded using the ‘ROI Color Coder’ plugin (BAR library, by T. Ferreira, http://imagejdocu.tudor.lu/doku.php?id=macro:roi_color_coder). In general, the colour scales were adapted for each experiment best reflecting the differences. Nuclei consisting of areas that were too small or those that had unrealistic high FRET ratios (owing to insufficient Aquamarine signal) were omitted (reflected as black in the colour coding).
Further information on research design is available in the Nature Research Reporting Summary linked to this paper.
All processed data generated or analysed during this study are included in this Article and its Supplementary Information. Imaging (Herud_et_al_2021__figures_3_and_4_raw_data) and in vitro source data (Herud_et_al_2021__suppl_figures_S1_S3-S5_S7_and_table_S2a_raw_data) are available at Zenodo (https://doi.org/10.5281/zenodo.4524537). The data for the FACS measurements in Fig. 3a, b and Extended Data Figs. 6, 7 can be found at https://flowrepository.org (FR-FCM-Z3FL). Coordinates and structure factors for all reported X-ray crystallography structures have been deposited in the PDB under accession codes 6EJW, 6EJZ, 6ENI, 6EKP, 6ENN, 6ELB, 6ELF and 6ELG. Materials (transgenic lines and plasmids) will be made available via the Arabidopsis Biological Resource Center (ABRC) in Columbus (OH, USA) and the Nottingham Arabidopsis Stock Centre (NASC), Nottingham (UK).
The ImageJ macros used to analyse data (Herud_et_al_2021__ImageJ_analysis_macros) are available from Zenodo (https://doi.org/10.5281/zenodo.4524537).
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We thank Addgene for distributing plasmids donated by W. Frommer, F. Merola, K. Beam and K. Thorn; O. Griesbeck, H. Schäfer, A. Holz, A.-C. Barragan-Lopez and C. Brancato for technical assistance; M. Perez Ortega for the initial steps towards the macro script; M. Belkacemi for sequencing of the variants; and M. Bayer for discussions and suggestions. C.F. thanks R. Palmisano and M. Küppers for help with gravitopism kit design. O.H.-S., M.K. and C.F. thank the staff of the Light Microscopy Facility at MPI for Developmental Biology for their support. G.J. thanks R. Hertel for discussions on auxin-related matters. We further thank the beamline staff at the Swiss Light Source and at BESSY for support. B.H. acknowledges the financial support and the allocation of synchrotron beam time by HZB as well as funding by the Deutsche Forschungsgemeinschaft (grant HO 4022/2-3). This study was supported by the Max Planck Society.
Open access funding provided by Max Planck Society.
The authors declare no competing interests.
Peer review information Nature thanks Richard Napier and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Extended data figures and tables
Extended Data Fig. 1 FRET response of several binding-domain variants to increasing substrate concentration.
a, Wild-type TrpR. b–q, Engineered TrpR variants. Each mark indicates a single measurement. Circle, IAA; rhombus, TRP; square, IAN.
a, Structure of IAA in the binding pocket of TrpR(M42F/T44L/T81I/S88Y). b, Structure of IAN bound to the same variant as in a. c, Overlay of IAA in TrpR(T44L/T81M/S88Y) (magenta) and TrpR(T44L/T81M/N87G/S88Y) (green). d, Structural overview of variants TrpR(T44L/T81M/N87G/S88Y) (green), TrpR(T44L/T81M/S88Y) (magenta), and TrpR(M42F/T44L/T81M/N87G/S88Y) (AuxSen, gold). It is apparent that AuxSen differs from the two intermediate structures regarding the overall arrangement of the helices. e–g, The structure of TrpR(S88Y/T44L) and all variant structures based on it show a slight relocation of the backbone of residues 70–90. This is probably due to the fact that all structures based on this variant crystallize in the orthorhombic space group P212121 (f) as opposed to the tetragonal space group P43 found for TrpR–IAA and TrpR(S88Y)–IAA (e). Both geometries have been found in earlier crystal structures of TrpR, for example PDB 1ZT9 (tetragonal) and 2OZ9 (orthorhombic). It seems that the introduction of the T44L mutation strongly favours crystallization in the orthorhombic geometry. In the P212121 space group, crystals form more extensive crystal contacts. The structure overlay (g) shows how several residues are displaced (residues that have symmetry mates within 3 Å are shown in red, and the ligand IAA is shown in green). However, interactions and positioning of the ligands are maintained. Nonetheless, we only compare backbone coordinates between variants of the same space group, to exclude misinterpretations due to crystal contacts.
a, Change in FRET ratio upon IAA treatment plotted against the dissociation constant (Kd) of the same variant as determined by ITC. b, FRET ratio changes do not correlate with the Förster distance. Blue–yellow pairs are marked in green, yellow–red pairs are in orange. Blue–yellow pairs, in general, show a higher FRET ratio change upon IAA treatment, but a similar range of Förster distances as the yellow–red ones. c, FRET ratio changes (in per cent) of several variants tested with two different fluorophore pairs. Variants showing a strong response with one fluorophore pair usually also show a strong response with another pair (correlation coefficient = 0.6). d–j, Effects of mutations in linkers. d, Structure of the construct. The IAA-binding TrpR variants were cloned as tandem repeats into the construct containing donor and acceptor fluorophores, analogous to ref. 18. The positional effect of the fluorescent proteins probably stems from slight rearrangements of the overall backbone in both TrpR subunits. Predominantly, this involves helix E of the reading-head motif, which mediates the DNA interaction in the natural function of TrpR. Because helix E is towards the C-terminal end of the chain, is it thought that fluorescent proteins positioned at this end will experience a larger positional relocation and thus show a more dynamic range of the FRET signal. e–g, First-round linker mutations. All three linkers were mutated, but no pattern for the optimal linker length could be determined. One linker II variant was chosen for further mutations. h, i, Second-round linker mutations. Linkers I and III were mutated in the variant obtained in the first round, with no changes in the optimized linker II. j, Third-round linker mutations. Linker I was further mutated in the variant containing mutations in linkers II and III. The linker length axis indicates the number of amino acid residues.
a, The FRET ratio is slightly affected by changes in the pH, but fully functional in the range of pH values within the plant cell. Red, pH 6.0; blue, pH 6.5; green, pH 7.0; violet, pH 7.5; cyan, pH 8.0. b, The FRET ratio is not strongly affected by salts and changes in the redox potential. Black, control; red, 1 mM (NH4)2SO4; blue, 1 mM CaCl2; green, 10 mM NH4NO3; violet, 10 mM DTT; cyan, 10 mM H2O2; yellow, 10 mM KCl; orange squares, 10 mM KNO3; orange diamonds, 10 mM NaCl. c, ITC data of AuxSen binding to IAA, measured at different pH values. Data are mean ± s.d., derived from 3 technical replicates.
a–j, Compounds with weak affinities; k–v, compounds with no affinity. The change in FRET ratio (y axis) is plotted against increasing concentrations of the individual compounds in μM (x axis). Each mark indicates a single measurement.
Cell-suspension-culture protoplasts were transfected with pJIT60-2xp35SS:NLS:AuxSen and the FRET response was captured by flow cytometry as the ratio of the emission between the Aquamarine peak intensity (FL9) and mNeonGreen peak intensity (FL10) as ‘Log_Height’ (a.u.). a, Normalized excitation and emission spectra for mNeonGreen and Aquamarine. The 405-nm laser line is shown as a vertical bar and bandpass filters are shown as open boxes, as rendered by FPBase44. As FRET occurs, the emission output is shifted from the FL9 to the FL10 bandpass. b, Baseline level of AuxSen FRET response, without exogenous IAA. c, Maximal response level of AuxSen with 10 mM IAA.
Extended Data Fig. 7 Demonstration of relevant population regions and Aquamarine, mNeonGreen and AuxSen fluorescent emission in cell-suspension-culture protoplasts.
Bivariate plots from left to right are as follows: forward versus side-scatter log area ungated; emission peak to shoulder FL1 (534/30) versus FL2 (585/29); forward versus side-scatter log area with cells of interest marked and gated for b–d; emission peak-to-shoulder FL9 (465/30) versus FL10 (529/28). Arrows indicate ‘gating’, meaning that the following plot is restricted to those data points that fall within that particular window. a, Cells only transfected with water. b, Cells transfected with pJIT60-2xp35SS:NLS:Aquamarine. Cells expressing Aquamarine were used to determine which scattering population produced the fluorescent protein. This gate is followed for mNeonGreen emission. c, Cells transfected with pJIT60-2xp35SS:NLS:mNeonGreen. Cells expressing mNeonGreen were used to determine which scattering population produced the fluorescent protein. This gate is followed for Aquamarine emission. d, Cells transfected with pJIT60-2xp35SS:NLS:AuxSen. Cells expressing AuxSen identified by their mNeonGreen emission then restricted to the ‘cells of interest’ scattering population that produced the greatest amount of protein. The FRET-response region was then made to encompass the entire range of possible fluorescence, including the shift in the FL9 to the FL10 bandpasses. See also Supplementary Table 2. Flow cytometry basic gate statistics and FRET-ratios based on (‘FL10-Log_Height’/‘FL9-Log_Height’) ratio are plotted against time for the final gate FRET response.
Extended Data Fig. 8 Quantitative analysis of PIN mRNA accumulation in seedlings treated with 10 μM IAA.
Seedlings were kept in MS medium (control; 0 min, purple) or transferred to a solution containing 10 μM IAA. RNA was extracted from 6 seedlings each after 10 min (blue) or 60 min (orange) and subjected to analysis by quantitative PCR with reverse transcription. Data are mean ± s.d. derived from 3 technical replicates, and black dots represent individual values.
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Herud-Sikimić, O., Stiel, A.C., Kolb, M. et al. A biosensor for the direct visualization of auxin. Nature 592, 768–772 (2021). https://doi.org/10.1038/s41586-021-03425-2
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