Molecular Crowding Tunes Material States of Ribonucleoprotein Condensates

1Ribonucleoprotein (RNP) granules or particles are a diverse group of subcellular compartments that are utilized by eukaryotic cells to spatiotemporally organize various biomolecular processes. These non-membranous assemblies, also termed as membraneless organelles (MLOs), dynamically form, dissolve, and tune their physicochemical microenvironment in response to changing cellular cues. RNP granules are enriched in proteins with low-complexity domains (LCDs) that are structurally disordered, and are assumed to be formed by RNP liquid–liquid phase separation (LLPS). LLPS is a spontaneous physical process that results in the formation of co-existing liquid phases of varying densities from a homogeneous solution. At the molecular level, low-affinity multivalent interactions amongst different LCDs and their partner nucleic acids provide the necessary energetic input to drive the LLPS of RNPs. Furthermore, LCD-mediated promiscuous interactions can act synergistically with sequence-specific interactions in many RNPs, thereby shaping their global phase behavior. Experimentally, it was observed that these promiscuous interactions are tuned by several cellular physicochemical perturbations (e.g., pH, salt concentration, and non-specific interactions with biomacromolecules).

2Unlike in typically utilized in vitro experimental conditions, in cellulo environments are crowded by a plethora of macromolecules that are ubiquitous within the cellular milieu. To effectively capture biomolecular dynamics in a crowded cellular environment, in vitro studies utilizing recombinant proteins employ buffer systems containing inert biocompatible polymers as crowding agents. One of the most widely used crowders is polyethylene glycol (PEG), a neutral hydrophilic polymer with numerous applications in crystallography, biotechnology, and medicine. Macromolecular crowding by PEG and similar polymer agents imparts a significant excluded volume effect (i.e., a space occupied by one molecule cannot be accessed by another) and results in alterations of molecular and mesoscale properties of biomolecules. For example, molecular crowding was shown to affect protein conformation, RNA folding, conformational dynamics of intrinsically disordered proteins, energetics of protein self-association, molecular recognition, and LLPS of globular proteins. However, how macromolecular crowding alters disordered RNP condensation remains underexplored.

3The well-established excluded-volume model of colloid–polymer mixtures predicts that the addition of a polymer chain to a neutral colloidal suspension will trigger inter-colloid attraction. The underlying driving force, known as the depletion interaction, is originated due to a net entropy gain by the system via maximizing the free volume available to the polymer chains. For globular protein–crowder mixtures, this depletion interaction can induce various phase transition processes, including protein crystallization. In a similar vein, for RNP systems containing low-complexity “sticky” domains, a considerable impact of macromolecular crowding on their phase transition is expected. This idea is supported by multiple recent observations such as (i) crowding induces homotypic LLPS of the nucleolar phosphoprotein Npm1 in vitro, (ii) PEG induces a robust liquid phase transition of the Alzheimer’s disease-linked protein Tau, and (iii) macromolecular crowding results in a substantial decrease in protein concentration required for inducing hnRNPA1 phase separation. However, it remains unknown whether molecular crowding impacts the fluid dynamics of RNP condensates.

4The material properties of intracellular RNP granules are important determinants of their function in intracellular storage and signaling. Notably, many RNP condensates are competent to mature into a fiber-like state, which is implicated in several neurological diseases. While the roles of LCD sequence compositions and charge patterns in controlling mesoscale dynamics of the RNP condensates have been the subject of some recent investigations, little is known regarding the effect of generalized thermodynamic forces such as crowding on RNP condensation. Here we conduct an experimental study to evaluate the impact of macromolecular crowding on the RNP liquid–liquid coexistence boundary, condensate fluidity in the micron-scale, and transport property by RNP diffusion in the nano-scale. Utilizing an archetypal RNP, fused in sarcoma (FUS), as well as representatives of the two commonly occurring LCD sequences in eukaryotic RNPs, we demonstrate an important role of crowding in modulating the mesoscale fluid dynamics of RNP condensates.

5Initially, we chose to study the effects of molecular crowding on the phase behavior of FUS using PEG8000 at concentrations that mimic cellular macromolecular density (≥150 mg/mL). FUS is a stress-granule-associated RNP that undergoes LLPS in vitro and in cellulo via attractive inter-protein interactions. Persistent FUS condensates also mature into a solid-like state during aging that is augmented by amyotrophic lateral sclerosis (ALS)-linked mutations. Therefore, FUS serves as an ideal model system for this study. Firstly, we tested the impact of crowding on the liquid–liquid coexistence boundary of the full-length FUS (FUSFL) in a physiologically-relevant buffer (25 mM Tris, 150 mM NaCl; pH 7.5) with variable PEG8000 concentrations. We used solution turbidity measurements in conjunction with optical microscopy to construct a phase diagram of FUSFL–PEG8000 mixtures, which is presented in Figure 1a. We observed that FUSFL formed micron-scale phase-separated droplets in vitro at protein concentrations ≥2 μM without any crowding agents (Figure 1), consistent with the protein’s ability to undergo LLPS at physiologically relevant concentrations. Increasing PEG8000 concentration in the buffer solution from 0 to 150 mg/mL decreased FUSFL phase separation concentration to <1 μM (Figure 1a). These results suggest that crowding by PEG8000 facilitates FUSFL condensation.

6The observed effect of PEG on lowering the RNP liquid–liquid coexistence boundary can be explained by a crowder-mediated depletion force that effectively increases the net inter-RNP attractive interaction with increasing concentrations of the crowder (also see Note S1). If that is the case, we expect that the fluidity of RNP droplets will decrease with increasing macromolecular crowding due to the enhanced inter-molecular network strength within the condensed phase. A similar phenomenon is known to drive colloidal gel formation in polymer–colloid mixtures. In the case of the RNP condensates, we expected a considerable alteration in the mesoscale dynamics, such as the biomolecular diffusion rate, with increasing PEG. Therefore, we next investigated the physical properties of the FUSFL condensates as a function of PEG8000 concentration at a fixed protein concentration (10 μM; Figure 1b–d). We used two complementary methods to probe FUSFL condensate material states: (a) Fluorescence recovery after photobleaching (FRAP), and (b) controlled fusion of suspended droplets using a dual-trap optical tweezer. Using FRAP, we measured the half-time of fluorescence recovery of the fluorescently-tagged RNP (Alexa488-FUS) after photobleaching a circular region at the center of the droplet (Figure 1b,c and Figure S1). Analysis of the and effective bleach radius (re) allowed us to estimate an apparent diffusion coefficient (Dapp) of a fluorescently tagged RNP within the protein-dense phase (see SI methods and Figure S1). The fraction of the mobile phase was also estimated from FRAP data and was used as a relative measure of the viscoelastic properties of FUSFL droplets. With increasing PEG8000, our FRAP data revealed two distinct trends (Figure 1b–d): (i) An increase in the fluorescence recovery half-time and, hence, a concomitant decrease in molecular diffusivity dynamics; and (ii) a decrease in the fraction of the mobile phase. The observed molecular diffusion rate decreased nearly fourfold upon increasing the PEG8000 concentration from 0 to 150 mg/mL. Concurrently, total fluorescence recovery after bleaching decreased from 100% to ~40% for FUSFL droplets. These data suggest that macromolecular crowding mediates a progressive transition of FUSFL droplets from a viscous fluid state to a viscoelastic state, resulting in substantially arrested protein diffusion.

7To gain further insight into the altered physical properties of FUSFL droplets in the presence of macromolecular crowders, we performed quantitative droplet fusion experiments using a dual-trap optical tweezer. In these experiments, we used one laser beam to hold one RNP droplet at a fixed position while another RNP droplet, trapped by a second laser, was moved towards the first droplet at a constant velocity (Figure 2a and Figure S2). As these droplets were brought into proximity, liquid FUSFL droplets coalesced rapidly in the absence of any crowders with a timescale of ~200 ms/μm (Figure 2, top panel; movie S1). In the presence of 150 mg/mL PEG8000, the fusion events of FUSFL droplets were almost arrested (incomplete fusion in Figure 2, bottom panel; movie S3). Instead, we observed that FUSFL droplets clustered at the optical trap under this condition (Figure S3). These observations are consistent with our FRAP results (Figure 1b–d). Taken together, our experimental data suggest that macromolecular crowding by PEG leads to a substantial hardening of FUSFL droplets. We note that the observed alteration in the material properties of FUSFL condensates occurred in the presence of crowding without any conclusive evidence for fiber formation (Figure S4).

8The phase separation of the FUS family of RNPs is assumed to be driven by enthalpy, that is, attractive protein–protein interactions, and, therefore, is sensitive to LCD sequence features that encode essential intermolecular interactions. As such, recent studies focused on elucidating the sequence determinants of LLPS in RNPs, which revealed two major classes of LCDs. These are (i) prion-like LCD (PrD), characterized by an overabundance in polar (S/G/Q) and aromatic (Y/F) residues but largely devoid of charged amino acids; and (ii) arginine-rich polycationic LCD (R-rich LCD), such as the disordered RGG-box sequences present in the RNA-binding domains of many RNPs. In the ribonucleoprotein FUS, both of these LCD types (FUSPrD and FUSRGG) are present as individual domains in the N- and C-termini of the protein, respectively (Figure 3a; Supplementary Table S1). To gain a mechanistic understanding of the impact of crowding on the physical properties of RNP droplets formed by these distinct LCDs, we next studied the phase behavior and physical properties of FUSPrD and FUSRGG condensates independently. FUSPrD is intrinsically disordered, as predicted bioinformatically (Figure 3a) and verified experimentally. FUSPrD is also known to form amyloids in vitro that contain dynamic β-sheet-rich structures, the formation of which is assumed to facilitate the droplet aging process. While FUSPrD has been implicated as the major driver of FUS LLPS, the role of FUSRGG in RNP condensation is only beginning to be explored. Similar disordered RGG-box regions have previously been shown to form homotypic condensates. Here, to study the effect of crowding, we first constructed phase diagrams of PEG–LCD mixtures for these two distinct LCDs separately. Both LCD types underwent concentration-dependent reversible phase separation upon lowering the solution temperature (Figure S5), suggesting that there exists an upper critical solution temperature (UCST) for these two disordered domains, above which a homogeneous phase is energetically favored. The UCST phase behavior for the two LCDs also indicates that their phase separation is driven predominantly by favorable free energy change during self-association via attractive protein–protein interactions. In presence of PEG8000, we observed that the phase separation of both FUS LCDs are facilitated. The isothermal phase diagram (at 22 ± 1 °C) analyses for FUSPrD and FUSRGG as a function of PEG8000 are presented in Figure 3. We observed that PEG decreased the protein condensation critical concentration by approximately fivefold for FUSPrD in response to an increase in the PEG concentration from 0 to 100 mg/mL. A similar trend was also observed for FUSRGG, where the concentration required for the protein to undergo LLPS was decreased by approximately sevenfold in the presence of 100 mg/mL PEG. These results are consistent with the hypothesis that the crowder-mediated depletion force acts synergistically with the homotypic LCD–LCD interactions (see Note S1).

9During the visualization of FUSPrD and FUSRGG condensates using a confocal fluorescence microscope, we noted that the well-dispersed LCD droplets underwent clustering at higher PEG concentrations (Figure S6). This observation indicates a crowding-dependent change of condensate physical properties. Therefore, we next investigated LCD droplet material properties in the presence of macromolecular crowders. Using Alexa488-labeled LCDs, we quantitatively analyzed fluorescence recovery after photobleaching in a well-defined region within FUSPrD/FUSRGG droplets (Figure 4). The recovery of fluorescence was modelled based on the diffusion of LCDs within the respective condensed phases (Figure S1). For FUSPrD droplets, FRAP analyses revealed that the diffusion rate decreased significantly with an increase in the PEG8000 from 0 to 175 mg/mL. Only ~20% fluorescence recovery was observed at ≥150 mg/mL PEG8000 in a timescale of 300 s after bleaching (Figure 4a–c). The FUSRGG droplets showed a similar arrest in protein mobility at a high concentration of PEG8000 (Figure 4d–f), although the changes were observed to be more gradual compared to FUSPrD. We speculate that the differences observed in the FRAP trend between FUSPrD and FUSRGG as a function of crowder concentration is a manifestation of sequence-encoded distinct molecular interactions and polypeptide chain dynamics in respective LCDs. We also note that FUSFL FRAP data (Figure 1b) showed a gradual change with increasing crowder concentration, similar to FUSRGG. Overall, these data suggest that both FUSPrD and FUSRGG droplets undergo progressive hardening with increasing PEG, despite their diverse sequence features and charge patterning.

10Macromolecular crowding in a cell arises from biopolymers with a plethora of sizes and shapes. In order to evaluate the excluded volume effect on RNP LLPS, it is necessary to use polymer crowders with variable chain lengths. Therefore, we next considered the impact of crowders with different molecular weights on the FUSFL condensation. To this end, we employed PEG polymers with molecular weights ranging from 300 to 35,000 gm/mol. FRAP experiments revealed that FUSFL droplets were viscoelastic in the presence of all the crowders tested (crowder concentration = 150 mg/mL), with a significant degree of arrest in the dynamic exchange of the fluorescently tagged RNPs (Figure 5a and Figure S7b). Dextran, another widely utilized molecular crowder with a different chemical identity, also showed similar effects on FUSFL condensates (Figure 5c and Figure S7d). These data collectively suggest that our observed viscoelastic tuning of FUS condensates is generally applicable to a broad range of polymer crowders and, therefore, represents a common effect of depletion interaction as induced by macromolecular crowding.

11Intracellular RNP granules are phase-separated bodies that display characteristic dynamics of complex fluids. The mesoscale physical properties of RNP condensates are important modulators of their functions. Aberrant alterations of the droplet material states, such as age onset loss of granule fluidity and formation of solid-like assemblies, are implicated in various neurological disorders, including ALS and frontotemporal dementia (FTD). Over the past two years, considerable efforts have been dedicated to characterizing RNP sequence-encoded molecular interactions that control the material properties of the RNP condensates. In this study, we considered the role of molecular crowding—a ubiquitous thermodynamic force in the cellular environment—on the RNP condensate dynamics. We experimentally showed that crowding, as mimicked by biocompatible “inert” polymers, not only lowered the LLPS boundary, but also substantially altered the exchange dynamics of the RNP within the condensed phase. We observed that the aforementioned effects of crowding on LCD-driven LLPS, namely facilitating liquid condensation and droplet hardening, were largely independent of respective disordered domain sequences. In other words, while the saturation concentration and the condensate physical properties are governed by polypeptide sequence composition and patterning, their alterations by molecular crowding were observed to be a common effect in both types of LCDs. To provide a mechanistic picture of the observed effect of crowding on the RNP condensation, we consider a thermodynamic model that describes the perturbation of protein–protein interactions by a crowder in light of the well-established excluded volume effect. According to this model, the introduction of a polymer crowder in the RNP–buffer solution leads to an isotropic inter-protein attraction by the depletion force (see Note S1), which acts in tandem with the intrinsic LCD–LCD homotypic attraction. The physical origin of the depletion attraction is the exclusion of the center of mass of a crowder molecule from a region surrounding an RNP molecule, which is typically called the depletion layer (Figure 6). The depletion layer thickness is directly proportional to the hydrodynamic radius of the polymer crowder. This simple thermodynamic model predicts that increasing crowder concentration in the solution will increase the overlap of the RNP depletion layers in order to produce excess free volume available to the polymer crowders (Figure 6). This implies that the net attractive LCD–LCD attraction is enhanced by macromolecular crowding, which lowers the critical concentration of RNP LLPS and results in hardening of RNP condensates. Mathematically speaking, as the concentration of PEG increases, the chemical-potential derivative,, which provides a thermodynamic basis of inter-protein attraction, decreases monotonically (see Equation (4) in Note S1). This quantity defines the spinodal curve, which is the boundary between the stable and unstable regions of the protein–crowder–buffer system (Figure S8). When, the system is stable as a homogeneous solution, whereas it phase-separates into two coexisting liquids if. Therefore, the net effect of the crowder may be physically interpreted as an effective increase in FUS–FUS attraction, manifested by depletion interactions. One key prediction of this model is that RNP partitioning in the dense phase should increase with increasing crowding (Figure S8). An increase in partitioning theoretically means a longer tie line that causes the volume fraction of the RNP in the dense phase to increase with a simultaneous decrease in the RNP volume fraction in the dilute phase. This is directly related to the strength of the inter-protein interaction parameter which increases the curvature of the free energy surface, pushing the coexisting states further apart (Figure S8). This was indeed experimentally verified for FUSFL condensates using confocal fluorescence image analysis, which indicated that the RNP partition increased by about fourfold in response to an increase in the PEG8000 concentration from 0 to 150 mg/mL (Figure 5d). This observed increase in partition coefficient suggests that FUSFL droplets become more dense with increasing crowder concentration. Such an increase in partitioning may also influence the rate at which FUSFL condensates mature into a solid phase, which has been previously shown to accelerate with increasing FUSFL concentration.

12In summary, we demonstrated that depletion interaction, as induced by macromolecular crowding, continuously tunes the physical properties of RNP condensates ranging from purely viscous fluids to viscoelastic gel-like states. Alteration in the material properties of phase-separated membraneless compartments inside cells has been previously observed both in normal physiology and pathology. Our results suggest that the hardening of RNP condensate is considerably influenced by the entropic forces in the crowded cellular environment. Several recent reports focused on identifying key RNP sequence features, post-translational protein modifications, and the role of RNA/protein partner binding that contribute to the gelation of RNP droplets. Based on the data presented here, we postulate that generalized thermodynamic forces that can tune effective RNP homotypic interactions are likely to influence the rate at which physiological condensates mature into a viscoelastic gel.

13Codon optimized wild-type full-length FUS (FUSFL), prion-like domain of FUS (FUSPrD; AA: 1-173), and the RNA-binding domain of FUS without the zinc-finger domain (FUSRGG:211-526Δ422-453) were gene synthesized by GenScript USA Inc. (Piscataway, NJ, USA) and cloned into (cloning site: SspI-BamHI) pET His6 MBP N10 TEV LIC cloning vector (2C-T). The plasmid vector was a gift from Scott Gradia (Addgene plasmid # 29706). TEV-cleaved proteins contained three exogeneous amino acids (SNI) at its N-termini. E. coli cells (BL21(DE3)) were transformed with the plasmids containing FUSFL and its variants in respective cases. Transformed cells were induced with IPTG (0.5 mM final concentration) at OD = 0.6–0.8 and further grown for an additional 3–5 h at 30 °C. Protein extraction was performed using a french press in lysis buffer (50 mM Tris-HCl, 10 mM imidazole, 1 M KCl, pH 8.0) containing protease inhibitor cocktail (Roche). Cell debris were removed by centrifugation. His-tag proteins were purified from the crude cell lysate using Ni-NTA agarose matrix (Qiagen Inc, Valencia, CA, USA) by gravity-flow chromatography following the manufacturer’s protocol with the following modifications: the wash buffer included 1.5 M KCl to disrupt nucleic acid binding to the recombinant protein, which was eluted with elution buffer containing 250 mM imidazole and 150 mM NaCl. The purity of the eluted protein samples was checked using A280/A260 measurements (to rule out presence of nucleic acids), and by polyacrylamide gel electrophoresis (PAGE) and Coomassie blue staining. The eluates (individual or pooled) were dialyzed against 25 mM Tris-HCl, pH 7.5 buffer containing 10% glycerol. The concentration of the protein samples were determined by absorbance at 280 nm using the following extinction coefficients: 103,600 M−1.cm−1 for FUSPrD-MBP, 86,750 M−1·cm−1 for FUSRGG-MBP, and 138,000 M−1·cm−1 for FUSFL-MBP (https://web.expasy.org/protparam). The protein samples were flash frozen in small aliquotes and stored in −80 °C.

14The S86C variant of FUSPrD and A313C variant of the FUSRGG were expressed and purified using an identical protocol as described above for the WT protein, except one modification: all buffers contained 2 mM DTT. The protein samples were fluorescently labeled with Alexa488 dye (C5-maleimide derivative, Molecular Probes) using Cys-maleimide chemistry as described in our earlier work. The labeling efficiency for all samples were observed to be ≥ 90% (UV-Vis absorption measurements), and no additional attempt was made to purifiy them further, given that only labeled protein is observed in the fluorescence experiments.

15All of the protein samples were buffer exchanged into the phase separation buffer (25 mM Tris-HCl, pH 7.5) containing 150 mM NaCl unless otherwise noted. Prior to performing phase separation measurements, the His6-MBP-N10 tag was removed by the action of TEV protease (1:25 ratio) (GenScript USA Inc.) for 1 h at 30 °C. The completion of the cleavage reaction was judged by polyacrylamide gel electrophoresis (PAGE) and Coomassie blue staining.

16Phase diagrams were constructed by turbidity measurements at 350 nm using a NanoDrop oneC UV-Vis spectrophotometer at room temperature (22 ± 1 °C). Desired amounts of PEG solutions were added to the protein solutions from a 35% (w/v) stock in nuclease-free water with appropriate salt concentrations. Each sample was incubated ~120 s prior to turbidity measurements using a 1 mm optical path length. Simultaneously, visualization of protein droplets (or lack thereof) was performed using a Primo-vert inverted iLED microscope (Zeiss), equipped with a Zeiss Axiocam 503 monochrome camera. A global analysis of the turbidity and microscopy data was performed to construct phase diagrams in respective cases based on a simple binary criterion that identifies if droplets were present at a given protein/PEG concentration.

17The fluorescence and DIC imaging were performed using a Zeiss LSM 710 laser scanning confocal microscope, equipped with a 63× oil immersion objective (Plan-Apochromat 63×/1.4 oil DIC M27) and a Zeiss Primovert inverted microscope. Samples were prepared and imaged using tween-coated (20% v/v) Nunc Lab-Tek Chambered Coverglass (ThermoFisher Scientific Inc.) at room temperature (22 ± 1 °C) unless otherwise noted, with ~ 1% labeled protein samples within the mixture of unlabeled proteins. All the samples were allowed to equilibrate in the chambered coverglass for ~30–45 min before imaging. For Alexa488-labeled samples, the excitation and emission wavelengths were 488 nm/503–549 nm; for Alexa594-labeled samples, the excitation and emission wavelengths were 595 nm/602–632 nm. Fluorescence recovery after photobleaching (FRAP) experiments were performed using the same confocal set up. The images and data were analyzed using Fiji software and the FRAP curves were plotted and analyzed using origin software (OriginPro 2018).

18FRAP experiments were performed using Zeiss LSM 710 laser scanning confocal microscope as described above. A circular region of interest (ROI) was bleached with 2–5 iterations of scanning using 100% laser power for a total time of 2–18 s. Fluorescence intensity changes with time were recorded for three different ROIs (bleached droplet, reference droplet, and background) for approximately 300 s or until the bleached ROI recovered and reached an equilibrium state. Data analyses were performed using Fiji software and MATLAB.

19The fluorescence intensities from bleached ROI were corrected for photofading by multiplying with a correction factor obtained from reference ROI as follows:: Initial intensity of reference droplet;: Intensity of reference ROI at time t;: Correction factor;: Intensity of bleached ROI at time t;: Intensity of bleached ROI (corrected for photofading) at time t.

20The corrected itensities were shifted to set the immediate post-bleach point to zero. which were then normalized.

21This normalized intensity post-bleach was plotted vs. time and fitted with a single exponential using MATLAB. Half time of recovery ( was obtained from the fitting parameter. To improve the goodness of the fit, two-exponential fit was also used. Half time of recovery ( was obtained graphically for the latter (Figure S1c,d).

22To account for diffusion during bleaching, instead of simply using user defined bleach radius (rn) for diffusion coefficient calculations, an effective radius (re) from the immediate post bleach frame was calculated by taking a profile across bleached ROI in Fiji. The normalized fluorescence intensities were plotted with distance and fitted with an exponential of a Gaussian laser profile using MATLAB, as previously described. re obtained from the fitting is the effective radius which corresponds to half width at 86 % of bleach depth K (Figure S1a,b).

23The apparent diffusion coefficient was calculated using the following equation:

24The mobile fraction was calculated using the following formula:: Fluorescence intensity after recovery;: Fluorescence intensity immediately after bleach;: Fluorescence intensity before the bleach.

25Controlled fusion assays were conducted to investigate changes in the material properties of the FUSFL condensates as a function of crowder concentration. The samples were injected into a 25 mm × 75 mm × 0.1 mm single chamber custom-made flow cell. Samples at 10 μM protein concentration were prepared with different PEG8000 concentrations and equlibrated for ~30 min at room temperature. The trap-induced fusion was done using a dual-trap optical tweezer system coupled with laser scanning confocal fluorescence microscope (LUMICKSTM C-trap). In a typical fusion experiment, two droplets were trapped with a 1064 nm laser with minimum power to reduce heating effect. The trapping of droplets was acheived due to a difference in the refractive index between the condensate and the dilute phase. After trapping, one droplet is brought into contact with the other droplet at a constant velocity of 40 nm/s. The trap remains traveling at that velocity until the fusion is completed and the final droplet relaxes to a spherical shape. The force on the moving trap was recorded at 78.4 kHz sampling frequency and analyzed using a fusion relaxation model. The following equation was used to fit the force-time curve: where the parameter is the fusion relaxation time. We scaled the fusion time by the average of the radii of the two droplets for every event. The linear term in the model is added to account for the constant trap velocity. First, we did a control experiment on a slow fusion sample and the relaxation times were obtained both from force curves as well as from aspect ratio analysis using fluorescence images. The results were in good quantitative agreement (data not shown). For FUSFL samples, at least 15 droplet fusion events were collected for each PEG concentration and the scaled relaxation times were averaged. An example of a typical normalized force curve with the fitted model is shown in Figure S2.

26Phase separated samples containing appropriate amount of fluorescently tagged protein were placed in a single-chambered custom-made flow cell (see Section 4.7). Droplets were imaged at the surface using laser scanning confocal fluorescence microscope using 60× water-immersion objective (LUMICKSTM, C-trap). Images were analyzed using Fiji software. To calculate the partition coefficient, the mean intensity of the entire droplet was divided by mean background intensity for several droplets per sample for statistical accuracy using Excel. Statistical analysis were carried out using MATLAB.

27To probe for amyloid-like structure formation within FUSFL condensates in presence of PEG8000 (150 mg/mL), we used a well-known amyloid reporter dye-Thioflavin T (ThT). 2–10 μM ThT probe was premixed with the experimental buffer (25 mM Tris. HCl, pH 7.5, 150 mM NaCl) used for FUSFL (10 μM) droplet formation in presence of the crowder. Simultaneous fluorescence imaging of FUS droplets were performed by using Alex594 labeled FUSPrD. Fluorescence imaging was performed using a Zeiss LSM 710 laser scanning confocal microscope. The excitation and emission wavelengths were 458 nm and 490 nm, respectively, with the exictation laser set at the same power as the Alexa594 channel.