- Open Access
Self-assembly/disassembly hysteresis of nanoparticles composed of marginally soluble, short elastin-like polypeptides
© The Author(s) 2018
- Received: 27 November 2017
- Accepted: 9 February 2018
- Published: 17 February 2018
Elastin-like polypeptides (ELPs) are a fascinating biomaterial that has undergone copious development for a variety of therapeutic applications including as a nanoscale drug delivery vehicle. A comprehensive understanding of ELP self-assembly is lacking and this knowledge gap impedes the advancement of ELP-based biomaterials into the clinical realm. The systematic examination of leucine-containing ELPs endeavors to expand existing knowledge about fundamental assembly–disassembly behaviours.
It was observed that these marginally soluble, short ELPs tend to behave consistently with previous observations related to assembly-related ELP phase transitions but deviated in their disassembly. It was found that chain length, concentration and overall sequence hydrophobicity may influence the irreversible formation of sub-micron particles as well as the formation of multi-micron scale, colloidally unstable aggregates. Amino acid composition affected surface charge and packing density of the particles. Particle stability upon dilution was found to vary depending upon chain length and hydrophobicity, with particles composed of longer and/or more hydrophobic ELPs being more resistant to disassembly upon isothermal dilution.
Taken together, these results suggest marginally soluble ELPs may self-assemble but not disassemble as expected and that parameters including particle size, zeta potential and dilution resistance would benefit from widespread systematic evaluations. This information has the potential to reveal novel preparation methods capable of expanding the utility of all existing ELP-based biomaterials.
- Elastin-like polypeptides
- Dynamic light scattering
- Inverse temperature transition
- Dilution stability
Elastin-like polypeptides (ELPs) are a fascinating biomaterial resulting from the fusion of the fields of biology, biochemistry and engineering. Based upon a highly repetitive sequence derived from mammalian elastin, ELPs are a versatile, customizable, stimuli-responsive biopolymer capable of self-assembling into a variety of architectures . The most common ELP is composed of any number of repeats of the pentapeptide sequence valine–proline–glycine–X–glycine (VPGXG) where X can be any amino acid except proline . This sequence can undergo a reversible phase transition in response to environmental stimuli and self-assemble into nano or micron-scale structures. There are a variety of stimuli capable of triggering this assembly including temperature, salt concentration, pH, light and the binding of a ligand, though temperature is the most commonly employed [3, 4]. The sequence and architecture of the ELP construct itself contributes substantially to the exact conditions required to trigger the phase transition, resulting in a flexible and programmable platform technology [5–8]. It is in part due to the relative ease of modification of the ELP family that it is a system under vigorous development for a wide variety of applications. ELPs are being developed for recombinant protein purification, tissue engineering and nanoscale targeted drug delivery [9–11]. There are numerous reviews in the literature detailing the myriad of ways in which ELPs are being engineered for specific applications [11–17].
Despite the widespread development of ELP-based biomaterials, the behaviour of ELPs is still not fully understood. For instance, the mechanism responsible for the reversible phase transition of ELPs is still an area of active investigation. The most recent models suggest that ELPs are intrinsically disordered and capable of momentarily adopting local beta-turn and polyproline structures both below and above their transition temperatures and that sudden decreased backbone solvation may cause ELP aggregation without affecting the structural fluidity of the individual ELP chains [18–24]. Some systematic studies have been carried out examining the effects of guest amino acid, chain length, concentration and pH on the transition temperature (Tt) of ELPs but the scopes of these studies have been limited either by the limited fidelity of early ELP synthetic techniques or by a focus on a narrow range of ELP constructs and particle characteristics [5, 25–33]. While this information may be somewhat useful for designing a construct for a specific temperature or pH trigger using the studied characteristics, these models are still limited in scope and there are other key parameters for which there is no systematic understanding.
Two properties of critical importance to the successful transition of ELP biomaterials to clinical applications like drug delivery include controlling particle size and zeta potential . These parameters are key factors in determining their biological fate and therapeutic efficacy, though no systematic observations have been made on how ELP sequence affects these parameters [34, 35]. Another factor critical to the success of ELPs as a delivery vehicle is their stability upon dilution . Concentration has been shown to affect transition conditions and as clinical administration usually involves diluting these materials within the blood compartment, it is important to understand their disassembly conditions. Other poorly understood aspects of ELP behaviour include whether existing trends in amino acid content, chain length and concentration effects on ELP Tt apply to increasingly hydrophobic constructs, the role of temperature treatment profiles in assembly characteristics, as well as a generalized understanding of ELP behaviour upon cooling.
This study begins to address these unknown parameters while simultaneously expanding upon the existing body of knowledge regarding systematically-studied behaviour of ELPs. The effects of chain length, amino acid chemistry and protein concentration were re-examined using a novel suite of short, highly hydrophobic ELPs developed by our group . ELPs composed of 20, 40, 80 or 160 pentapeptide repeats with leucine in the guest amino acid position, as well as a valine-containing 40-mer control, were studied across a range of concentrations and temperatures using dynamic light scattering (DLS), zeta-potential and transmission electron microscopy (TEM). ELP particle stability upon isothermal dilution was also investigated. The systematic approach undertaken herein allowed for the deconvolution of the effects concentration, guest amino acid chemistry and chain length have on assembly, disassembly and particle characteristics such as size, stability and ELP behaviour as well as advancing the body of evidence supporting clinical therapeutic use of ELPs.
ELPs were synthesized according to Bahniuk et al. . Briefly, the initial ELP genes were purchased through Integrated DNA Technologies (Coralville, IA, USA) and were concatemerized together in a pUC-19 cloning vector (Bio Basic, Ontario, Canada) using a modified recursive directional ligation procedure. The restriction enzymes PflMI and BglI (New England Biolabs, Ipswich, MA, USA) were used to create ELP inserts and vectors which were recombined multiple times to form ELP genes of various lengths. Additional digestions, gel purifications and dephosphorylation reactions were employed to ensure a minimum number of Escherichia coli (E. coli) XL10-Gold (Agilent Technologies, Santa Clara, CA, USA) needed to be screened.
ELP genes were inserted into a pET-25b(+) expression vector containing the N and C-terminal sequences for the ELP genes as well as a tobacco etch virus protease cut site and polyhistidine tag. The expression vector also contained two SfiI (New England Biolabs, Ipswich, MA, USA) restriction enzyme recognition sites with a spacer sequence in order to facilitate efficient vector linearization before ELP gene insertion. As with the concatemerization, additional restriction digests, gel purifications and dephosphorylation reactions ensured the cloning was as efficient as possible. DNA sequencing was carried out at the Molecular Biology Service Unit at the University of Alberta to confirm the ELP genes were correct then the expression plasmids were transformed into OneTouch E. coli BL21 (DE3) (Invitrogen, Carlsbad, Ca, USA).
ELP expression was performed by growing the E. coli in Terrific Broth (Thermo Fisher Scientific, Waltham, MA, USA) at 37 °C containing 100 µg/mL ampicillin (Thermo Fisher Scientific) and 10 mM l-proline (Sigma-Aldrich, St. Louis, MO, USA) and inducing expression with 2 mM isopropyl β-d-1-thiogalactopyranoside (Thermo Fisher Scientific) once the OD600 of the culture reached 0.8. Upon induction, the cells were left to grow at 37 °C, 225 rpm for 24 h. Cells were pelleted and frozen in liquid nitrogen before being subjected to denaturing metal-affinity chromatography purification. Buffered 8 M urea was used to lyse the cells and fully solubilize any ELP before binding them to nickel beads at 4 °C. After extensive washing the ELPs were eluted using a buffered imidazole step gradient. ELP-containing eluents were subjected to one round of inverse temperature cycling to complete the purification. When necessary, solid NaCl up to 1.5 M and/or temperatures of 37 °C were employed to trigger the phase transition of the ELPs. Exact conditions depended greatly on the construct and its concentration upon expression. No protease digestion was performed on the purified ELPs. Polyacrylamide gel electrophoresis was used to confirm the success of the purifications and sample concentrations were quantified using UV absorbance at 280 nm. The complete amino acid sequence for each ELP construct can be found in Additional file 1: Table S1.
ELP concentration values
ELP concentrations were normalized by mass in part to control the number of pentameric ELP subunits between samples and also due to technical limitations at both high and low molarities. The lower molarity limit for each ELP sample was dictated by the 0.01 mg/mL minimum sensitivity of the DLS instrument. Given the breadth of ELP lengths studied herein, this meant that the lowest reliably measurable molarity for L20 would be much higher than that of L160. Additionally, attempts to match the highest molarities of shorter constructs using longer ELPs were impeded by the requisite high mass concentrations and difficulties associated with concentrating ELPs to those levels and the resulting instability of the protein solutions, even at low temperatures.
ELP temperature trend DLS measurements
Thermal behavior of five ELP constructs (V40, L20, L40, L80 and L160) at concentrations of 0.05, 0.1, 0.5 and 1.0 mg/mL was studied using DLS (Malvern Zetasizer Nano ZS, Malvern Instruments Ltd, Malvern UK). Frozen ELP aliquots were thawed and diluted on ice with PBS pH 7.4 to the desired concentration. 100 µL of sample was placed in a 40 µL minimum volume DLS cuvette and kept cold on ice until measurement. ELP samples were equilibrated within the zetasizer at 5 °C before starting measurements. Samples were heated from 5 to 50 °C and subsequently cooled back to 5 °C. Size was measured at 5 °C intervals. A 2 min interval at each measurement temperature was programmed to allow for thermal equilibration of the sample. Two measurements, each with > 10 subruns were recorded at each temperature during heating and cooling. L20 samples at 0.5 and 1.0 mg/mL were sonicated on ice for 30 min prior to the temperature trend measurements to ensure that no particles carried over from the concentrated stock solution or had inadvertently formed during sample preparation. Absorbance, refractive index and viscosity of the PBS and ELP were calculated using Malvern’s zetasizer software 7.03. Protein analysis mode was used for all measurements. Measurement settings were automatically optimized at each temperature interval. Unless otherwise stated, all DLS data represents the peak position of the distribution of particle sizes. All aggregate distributions had polydispersity index (PDI) values < 0.2 unless the samples were actively undergoing a substantial change in particle diameter or the sample had been affected by particle precipitation.
ELP zeta potential measurements
Zeta potential of five ELP constructs (V40, L20, L40, L80 and L160) at concentrations of 0.05, 0.1, 0.5 and 1.0 mg/mL was determined using a Malvern Zetasizer Nano ZS. All measurements were performed at 5 and 37 °C. Frozen ELP aliquots were thawed in water then placed on ice immediately after thawing. ELPs were diluted with cold PBS pH 7.4 to make two 50 µL aliquots of each concentration. Note that L20 samples at 0.5 and 1.0 mg/mL were sonicated on ice before use as explained previously. All samples were kept on ice until use and ELP solutions, PBS buffer and sample cuvettes were equilibrated at 5 or 37 °C as needed before measurements were taken. A 40 V electrical potential was used to measure all samples. Three measurements of each sample were taken to ensure reproducibility. Each measurement had a minimum of 10 subruns, with a maximum of 60 subruns at 37 °C and 100 subruns at 5 °C. The diffusion barrier technique, details of which are available on the Malvern website, was used for all measurements. 35 µL of ELP was loaded into the bottom of a folded capillary zeta cell (Malvern Instruments Ltd, Malvern UK) already filled with PBS. The sample was then loaded in the instrument and measured immediately to minimize diffusion of the ELP. Absorbance, refractive index, viscosity and dielectric constant of the PBS and ELPs were calculated using Malvern’s zetasizer software 7.03.
ELP dilution DLS measurements
Nanoparticle size upon dilution of all ELP constructs (V40, L20, L40, L80 and L160) was measured using DLS (Malvern Zetasizer Nano ZS, Malvern Instruments Ltd, Malvern UK). Frozen ELP aliquots were thawed and diluted on ice with PBS pH 7.4 to a starting concentration of 1.0 mg/mL. 100 µL was pipetted into a 40 µL minimum volume DLS cuvette and allowed to equilibrate for 20 min at 37 °C in the zetasizer. Five repeats were collected, each with > 10 subruns used to collect the overall data. This ELP solution was then diluted to 0.5 mg/mL in the DLS cuvette with PBS (isotonic) pH 7.4 kept at 37 °C (isothermal) in a heat block. The sample was then allowed to equilibrate at 37 °C for 10 min before taking 5 measurements. The sample was subsequently diluted to 0.10 mg/mL and then 0.05 mg/mL using this process, taking five measurements at each concentration and allowing 10 min between dilutions. L20 was sonicated on ice for 30 min before measurement in order to ensure no nanoparticles were carried over from the concentrated stock solution or inadvertently formed during sample preparation. Absorbance, refractive index, and viscosity of the PBS and ELP were calculated using Malvern’s Zetasizer Software 7.03.
Transmission electron microscopy
Transmission electron microscopy (TEM) was carried out at the Cell Imaging Center at the University of Alberta. Samples for TEM were prepared as they were for temperature trend DLS measurements. The samples were heated in a Mastercycler gradient thermocycler (Eppendorf, Hamburg, Germany) under conditions identical to those during the temperature trend. 400 mesh carbon-coated copper grids (Ted Pella, Redding, CA, USA) were subjected to glow discharge in a Pelco easiGlow™ system (Ted Pella, Redding, CA, USA) at 0.4 mBar, 15 mAmp and positive polarity for 45 s. 10 µL samples were immediately placed on charged grids for 3 min incubations on an appropriately warmed heatblock (VWR International, Radnor, Pennsylvania, USA), before two rounds of washing in pre-warmed ultrapure MilliQ water (EMD Millipore, Etobicoke, Ontario, Canada) on the same heated surface. Unstained samples were then directly taken for TEM imaging on a Hitachi H-7650 TEM using a 60 kV accelerating voltage. Images were acquired using a 16 megapixel EMCCD camera (Advanced Microscopy Techniques) and processed using the AMT Image Capture Engine software version 602.576.
An unpaired Student’s t-test was used to evaluate the significance of differences between various results. The minimum level of significance was set to α = 0.05.
Increasing the concentration of L20 from 0.10 to 0.50 mg/mL changed the ELP behaviour considerably. Upon heating to 20 °C a drastic increase in particle size was observed (Fig. 1c), with results that were beyond the range of the DLS instrument (> 10 µm). Diameters at higher temperature suggested a particle size in the 2 µm range before decreasing to below 500 nm at 45 °C. Visual examination of the DLS cuvette after reaching 50 °C showed precipitation had occurred during the course of the temperature-dependent measurements. Cooling the sample down to 5 °C did not result in a resolubilization of the precipitated ELPs; supported by the fact that DLS results showed particle diameters did not decrease to < 10 nm. The numerical values for L20 diameters at and above the size shift temperature for the heating as well as the entire cooling may have been affected by the settling of larger particles and the upper sensitivity of the instrument. As such, the data from Panel C should only be interpreted to show that L20 at 0.50 mg/mL had a size shift at 20 °C after which very large aggregates formed and the ELP suspension became unstable. Cooling the sample back to 5 °C did not result in aggregate dissolution. The L20, 1.0 mg/mL system showed a large change in particle size at 15 °C and upon further heating, micron sized aggregates formed that, like the 0.50 mg/mL sample, grew too large to be reliably measured using DLS (Fig. 1d). This sample also displayed instability and precipitated protein was observed after heating to 40 °C and this remained even after cooling back to 5 °C. As such, the data obtained from heating at 45 and 50 °C and the subsequent cooling profile may have been affected by the sample instability.
Generally speaking, when a charge was observed, all ELPs were negative. This is consistent with the average charge of an individual ELP chain being slightly negative. In all cases increasing the temperature from 5 to 37 °C, that is, from below to above Tt for each ELP system resulted in an increase of the magnitude of the zeta potential decrease in the total surface charge of each sample regardless of concentration. This change in zeta potential was found to be statistically significant in many cases with the exceptions of L80 and V40 at 1.0 mg/mL. Concentration likely affected the zeta potential for soluble ELPs, where three of the five constructs tested showed an increasing negative charge. At 37 °C there did not appear to be any discernable relationship between ELP concentration and the zeta potential magnitude.
Overall the majority of the constructs tended to decrease in diameter as they were diluted from 1.0 to 0.05 mg/mL, the extent of which varied depending on the construct. Only L20 appeared to form larger, irreversibly precipitated particles as the sample became more dilute. Complete particle breakdown was not observed for any system as no diameters below 10 nm were observed; though the PDI for L40 became large enough to suggest some instability in that system upon a 20-fold dilution.
Transmission electron microscopy was carried out as a secondary assessment of ELP particle morphology and diameter. Each construct was examined at 0.10 mg/mL after heating in a manner consistent with previously discussed variable-temperature DLS experiments up to 35 °C. These conditions were chosen as all constructs were stable throughout their heating and cooling at this concentration and the temperature is in the range of biological significance. Additional samples were prepared for L20 and V40 at 1.0 mg/mL after heating to 50 °C in order to visualize the structures formed during precipitation.
ELP V40 particles at 0.10 mg/mL and 35 °C (Fig. 8) or 1.0 mg/mL and 50 °C (Fig. 9) were similar to the L-series: spherical structures were observed though they did not appear as electron dense as the L-series. At 0.10 mg/mL and 35 °C, the diameters of the V40 particles generally matched those measured with DLS, though the deviations from the mean size appeared larger for the TEM samples. This may be because the standard deviation value reported by the DLS instrument only represents the variance in the mean diameter over multiple measurements, rather than the total width of each measured size distribution. The lower overall charge of V40 particles may have also played a role in that their structures may have been stabilized less by the oppositely charged EM grid than the L-series and, consequently, may have been prone to greater variation in their size once sampled on the EM grid. At 1.0 mg/mL and 50 °C, the V40 structures on the TEM showed the lowest electron density of any sample and the structures resembled spheres that possibly were formed from lamellae of protein. Regardless of formation mechanisms these structures were unlike all other samples.
As explained in the “Methods” section, mass concentration was used to normalize the amount of ELP in each sample due in part to technical limitations. While this allowed for equivalent amounts of ELP pentamers to be present in samples of the same mass concentration, this does not take into account the effect of molarity. As such, considerations of molarity may be used to explain some of the observed behaviours when mass concentration cannot.
With only 20 repeats of the VPGLG amino acid sequence, the L20 ELP is the shortest construct examined with the relatively hydrophobic leucine in the guest amino acid position. Generally speaking, the concentration of L20 did affect the size of the particles formed above the transition temperatures. At a concentration of 0.05 or 0.10 mg/mL, particle size reached a maximum of approximately 650 nm during heating before decreasing to about 500 nm in diameter. At 0.10 mg/mL this decrease in particle diameter while heating as well as the reverse during cooling were found to be statistically significant (p < 0.0001). Increasing the L20 concentration to 0.50 or 1.0 mg/mL resulted in the formation of micron-scale aggregates which were not stable in solution and did not resolubilize upon cooling. The ELP concentration may have some effect on the transition temperature as it varied from 15 to 20 °C depending on the sample conditions, but there was no clear trend with this data set, possibly due to the 5 °C temperature resolution of the DLS program. L20 particle dissolution was not observed at any of the tested concentrations which implies the system exhibits some considerable hysteresis, in the range of 15–20 °C, though it cannot be fully quantified. The diameters of these particles were consistent across DLS and TEM samples. That L20, regardless of concentration, particle size or stability, did not disassemble seriously challenges the fundamental assumption that all ELP phase changes are reversible and that they fully disassemble upon cooling. The irreversible precipitation of L20 was also observed when examining the dilution stability, so the initial concentration-based precipitation is not reversed by sample dilution. This is unlike observations made in this study for V40 under an identical dilution treatment, nor is it consistent with turbidimetric analysis of dilutions performed on particles composed of repeats of elastin exons 20–24 . This property of irreversible precipitation was also seen during routine L20 purifications. Inverse temperature cycling-based purifications of L20 using standard procedures resulted in permanently precipitated samples when ELP concentrations were > 0.40 mg/mL. Additionally, stock solutions of L20 at these high concentrations were found to contain micron-sized aggregates immediately upon thawing (data not shown). These irreversible precipitates could only be successfully resolubilized by minimizing the time they were heated above their Tt during purification and subjecting samples to bath sonication on ice. There is no evidence to suggest that surface charge plays a role in the formation of large L20 aggregates, as zeta-potential values for the system above its transition temperature were all in the range of − 10.5 mV.
Increasing the ELP length from 20 to 40 repeats lead to some differences in the ELP temperature response and assembly behaviour. The concentration of L40 was shown to affect the size of the particles both in the heating and cooling phases. During the heating phase the average particle sizes increased from ~ 350 to 650 nm as the ELP concentration increased while during cooling the average size remained in the 400–450 nm range over the range of the tested concentrations. At no point were micron-sized particles observed. This can also be inferred by comparing the particle size measurements at 50 °C. For L40 the diameters for both heating and cooling are in good agreement, unlike cases when the sample underwent precipitation (i.e. L20 and V40). The Tt was also affected by the ELP concentration. At 0.05 mg/mL the L40 underwent its transition at 20 °C but at 0.10–1.0 mg/mL the ELPs transitioned at 15 °C. Hysteresis of the assembly/disassembly transition temperature was observed for all samples. As the 0.50 and 1.0 mg/mL samples did not fully disassemble upon cooling, a numerical value cannot be determined. For the 0.05 and 0.10 mg/mL samples the values for hysteresis were ~ 15 and 10 °C, respectively. As the more concentrated samples did not disassemble, there may be a concentration-dependence for the dissolution of the L40 system. Particle diameters measured using TEM agreed with DLS results for identical conditions. The zeta potential for L40 when heated above its Tt displayed some concentration dependence, with lower concentration samples having stronger charges. Dilution stability testing did not decisively show particle breakup, though increasing PDI values at 0.05 and 0.10 mg/mL dilutions suggest instability upon further dilution may be possible. This instability upon dilution is not consistent with the behaviour of any of the other ELPs tested herein. While studies of ELP particle stability upon dilution are severely lacking in the literature, Osborne et al. reported that an ELP construct composed of repeats of elastin exons 20–24 demonstrated particle dissolution upon dilution using turbidimetric methods, though the degree of dilution was not reported . ELP L40 behaviour upon dilution appears to fall between the results reported by Osborne and those made here using related L-series constructs.
L80 constructs self-assembled when heated to 10–15 °C to form 200 to 600 nm diameter particles, with both the Tt and particle size dependent upon ELP concentration. Lower concentrations generally resulted in smaller particles, though heating a 1.0 mg/mL solution to greater than 35 °C resulted in a statistically significant (p < 0.0001) decrease in particle size from ~ 500 to ~ 320 nm. Upon cooling, the particle diameters tended to remain steady and upon reaching 5 °C every tested concentration of L80 was shown to fully disassemble. Concentration dependence was observed for the L80 transition temperature during assembly but not disassembly. At 0.05 and 0.10 mg/mL the Tt was 15 °C and at higher concentrations the Tt decreased to 10 °C. Hysteresis was observed under all sample conditions except for 1.0 mg/mL, with a value ranging from 5 to 10 °C. Surface charge and dilution stability data suggest this was a stable construct in general, with no tendency to precipitate or destabilize upon dilution. TEM results confirm the sizes determined using other methods in that L80 presents as a spherical, electron dense particle that was well dispersed and not prone to aggregation.
ELP L160 was the largest tested construct (77 kDa) and in general, the concentration of L160 appears to have some effect on the diameter of the particles formed upon heating. Samples with lower concentrations of ELPs formed smaller diameter particles upon heating, with average diameters in the 250–300 nm range for 0.05 and 0.10 mg/mL samples and diameters in the 500–600 nm range for more concentrated samples. This same trend can be observed for the particle sizes when the samples were being cooled. As with other constructs, some statistically significant (p < 0.0001) decrease in particle diameter was observed for the 1.0 mg/mL sample upon heating above 35 °C. At a concentration of 0.50 mg/mL, L160 formed particles upon heating to 10 °C. The particle diameter remained consistent at ~ 200 nm until the sample temperature reached 25 °C, whereupon the particle diameters steadily increased to a maximum of ~ 625 nm. Cooling the L160 samples back to 5 °C resulted in very little variation in particle diameter until disassembly was observed at 5 °C for all ELP concentrations. Unlike other ELP constructs, each of the L160 samples did show complete disassembly upon cooling in a concentration independent manner. Concentration clearly affected the assembly Tt for this system. Transition temperatures ranged from 10 to 20 °C with more concentrated samples having lower transitions. Hysteresis was observed at 0.05 and 0.10 mg/mL and the value of the hysteresis ranged from 5 to 10 °C. The zeta potential values for this construct above its Tt ranged from − 10 to − 16 mV which suggests these particles should be colloidally stable. This was the only construct to show a greater zeta potential value at 37 °C as the concentration of L160 was increased. Additionally, diluting a sample of L160 particles from 1.0 to 0.05 mg/mL did not result in any meaningful fluctuations of diameter or large standard deviations indicative of decreased particle stability. Electron microscopy was consistent with the observations made with other techniques in that the particles at 35 °C and 0.10 mg/mL roughly matched the DLS observations and resulted in the formation of spherical, electron dense and well-dispersed structures. Previous studies suggested the uniform intensity observed for all L-series ELPs indicated the formation of a micelle-like structure .
ELP V40 underwent a phase transition upon heating to 30–35 °C, with higher concentration samples requiring less heating to elicit a response. Once above their transition temperature, V40 formed particles ranging in size from 200 nm to microns in diameter. TEM images suggested that the V40 was not as electron dense as leucine-containing ELPs, which may indicate that guest amino acid hydrophobicity influences packing density. Previous studies have shown that the packing density of assembled ELP above their Tt can be influenced by the phase transition of individual blocks in a block copolymer ELP, solution salt concentration and the distribution of hydrophilic and hydrophobic guest amino acids throughout a multiblock copolymer [27, 38, 39]. The results herein suggest that the role of guest amino acid hydrophobicity in ELP homopolymers may be another avenue by which to engineer the packing density of ELP particles for the needs of specific applications. While there was no clear relationship between ELP concentration and diameter for this system, it was evident that at concentrations of 0.50 and 1.0 mg/mL very large aggregates were formed quickly and precipitation was observed once the samples had been heated to 50 °C. This is consistent with the disagreement between sample diameters at 50 °C during heating and cooling. While this precipitation matches the behaviour for L20, unlike L20 the V40 precipitates resolubilized upon cooling to 5 °C and visible settling was no longer apparent. That this construct readily resolubilized was consistent with its observed behaviour during purification. Inverse temperature cycling procedures were able to precipitate and resolubilize the V40 normally, just like L40, L80 and L160. At 0.05 mg/mL the V40 particle size appeared to continually increase as the sample was heated and the reverse was observed upon cooling. Of all the V40 samples tested, 0.10 mg/mL most resembled the leucine-containing ELPs during its temperature trend. Upon assembly this sample formed structures 400–500 nm in diameter which significantly (p < 0.0001) decreased in size to ~ 175 nm upon heating to 45 °C. As also observed at 0.05 mg/mL, this behaviour was reversed during sample cooling. It appeared that regardless of sample concentration or particle size and solubility, cooling V40 down to as low as 5 °C resulted in complete ELP resolubilization, though large hysteresis values were observed for 0.10 mg/mL and especially 0.05 mg/mL V40. Compared to the leucine-containing ELPs, V40 had lower overall zeta potential values. Above its transition temperature, V40 only had a zeta potential of about − 6.5 mV which did not vary in conjunction with sample concentration. This charge value is low enough that sample precipitation would not be unexpected though precipitation was only observed for the more concentrated samples during the up to 3 h sample testing periods. As with L20 it appears that surface charge is not the only factor that contributes to the development of micron-scale aggregates and subsequent precipitation of ELPs. V40 also demonstrated further unusual behaviour relative to other tested constructs when its stability upon dilution was examined. This construct started off with a diameter of just over 1 μm at 1.0 mg/mL and steadily decreased in size with dilution to a final size of about 300 nm at 0.05 mg/mL, with the first dilution producing a significant decrease in particle diameter (p < 0.0001). Further dilution may result in observations consistent with previously examined ELPs . No other construct demonstrated such a large decrease in diameter. Interestingly, unlike the L20 which precipitated during this procedure, the dilution of V40 appeared to have reversed the growth of the aggregates and prevented their precipitation as no visible settling was observed for this construct. This may be related to the ease with which precipitated V40 can be resolubilized simply by cooling but L20 cannot.
Summaries of ELP assembly and disassembly behaviour upon heating and cooling as observed with DLS in 1X PBS pH 7.4 with heating and cooling in 5 °C increments
Tt heating (°C)
Tt cooling (°C)
Hysteresis (∆ °C)
Zeta potential (5 °C, mV)
Zeta potential (37 °C, mV)
− 0.882 ± 0.8
− 11.3 ± 0.6
No disassembly observed
− 1.27 ± 0.4***a
− 11.4 ± 1.0
No disassembly observed
− 7.04 ± 0.1***a
− 10.1 ± 0.4
Not all diameters quantifiable
− 7.04 ± 0.5
− 9.52 ± 0.8
Not all diameters quantifiable
− 3.47 ± 4.0
− 14.0 ± 0.5
− 6.10 ± 1.9
− 14.1 ± 1.4*b
− 0.233 ± 4.4
− 10.4 ± 0.2*b
No disassembly observed
− 5.38 ± 0.2
− 10.4 ± 0.9
No disassembly observed
− 9.53 ± 3.4
− 12.2 ± 0.8
− 5.25 ± 4.4
− 13.5 ± 2.5
− 4.22 ± 0.5*c
− 13.3 ± 1.6
− 8.89 ± 1.4*c
− 12.5 ± 1.9
− 0.242 ± 2.8**d
− 10.2 ± 1.1
− 1.71 ± 1.8
− 10.4 ± 2.6*e
− 2.37 ± 8.0
− 15.8 ± 1.1*e
− 8.06 ± 0.2**d
− 13.6 ± 0.6
0.344 ± 3.5
− 6.94 ± 1.6
− 0.834 ± 1.2
− 7.00 ± 0.14
− 1.37 ± 1.1*f
− 5.73 ± 0.3
Not all diameters quantifiable
− 3.90 ± 0.6*f
− 5.61 ± 0.9
Not all diameters quantifiable
By comparing the responses of L20, L40, L80 and L160 at equivalent mass concentrations, the effect of chain length for hydrophobic, short ELPs was elucidated. Consistent with previous reports in the literature, transition temperatures decreased with longer chain lengths, holding all other parameters constant . One of the most interesting results was that chain length may affect the size and stability of particles formed in solution and that the relationship between chain length and particle size is inverse. Longer ELPs were found to form smaller diameter particles when, given identical mass concentrations, there were equal amounts of ELP pentapeptide sequences between samples. The relationship between ELP chain length and particle diameter and the role of the quantity of ELP pentapeptides compared to the number of ELP molecules has never been explored in the literature previously. Longer ELPs appeared to more readily disassemble upon cooling compared to the shorter constructs, with L20 resolubilization not observed under any of the current tested conditions, limited by the lower mass sensitivity of the DLS instrument. The lack of observable L20 resolubilization herein may be explained by the relatively high molarity of the L20 samples compared to the longer ELP constructs. Some hysteresis was present during sample cooling, with larger discrepancies between assembly and disassembly temperatures for the shorter ELPs. The dilution stability results suggested that longer ELPs tended to retain their size better than shorter ones, though the precipitation of L20 during the dilution test limits the range of lengths that could be successfully tested in this manner. There were no discernable relationships between ELP chain length and surface charge, regardless of sample temperature, nor did there appear to be a correlation between length and ELP behaviour in response to cooling. All construct diameters remained stable until cooled to 5 °C. L20 was found to form larger particles in general and, at high concentrations, micron-scale structures which precipitated out of solution. L40, L80 and L160, composed of identical but longer sequences, consistently formed particles with sub-micron diameters without any solution stability issues over the course of the 3 h measurements. TEM observations were consistent with sizes measured using DLS and support the notion that chain length showed an inverse relationship with particle size for the leucine-containing ELPs.
A comparison of the responses of L40 and V40 can be used to extrapolate generalizations regarding the influence of guest amino acid residues. Clearly the more hydrophilic V40 had a higher Tt than the L40. This is generally in agreement with predictions described in previous literature, though there are some variations due to the different lengths of ELPs tested . V40 was also observed to form significantly larger particles upon heating compared to L40. So much so that the V40 even precipitated at 0.50 and 1.0 mg/mL while the L40 formed sub-micron particles with no observed stability issues during the ~ 3 h temperature trend testing. At concentrations where precipitation was not a concern, L40 tended to present as more consistently-sized particles while being heated. While being cooled, V40 sizes resembled those measured during the corresponding heating size trends while L40 particles had a relatively steady diameter with an abrupt change in size at ~ 5 °C. V40 also appeared to have larger hysteresis values than L40 when precipitation was not observed, with differences as large as 25 °C for V40 but only 15 °C for L40. There was no clear relationship between particle size and guest amino acid residue observed. Zeta potential of assembled particles, that is at 37 °C, did appear to be affected by the guest amino acid with the more hydrophobic L40 displaying a stronger negative charge at all concentrations compared to V40. TEM analysis revealed that the V40 construct was less electron dense that L40 which implies that a greater hydrophobicity may result in tighter packing of ELP chains .
The systematic analysis of a family of ELPs with varying guest amino acid hydrophobicity and/or chain length at several equivalent concentrations over a range of temperatures allowed for the deconvolution of the influence these various sample parameters have upon particle assembly behaviour and characteristics. This information can be broadly applied to the design of all future ELP-based materials and also can be used to expand the utility of existing ELP constructs. This novel family of hydrophobic ELPs behaved consistently with previously reported observations regarding the effects of guest amino acid chemistry, chain length and concentration on ELP assembly transition temperatures. The disassembly and hysteresis behaviour of this family of ELPs challenges the generalization that VPGXG-type ELPs disassemble and resolubilize upon cooling. Systematic experimentation revealed that chain length, concentration and guest amino acid hydrophobicity may all influence this irreversible assembly. The surface charge of the systems was shown to be influenced by the solubility state of the ELPs as controlled by temperature and also by the guest amino acid hydrophobicity. More hydrophobic guest resides may result in a greater density of ELP molecules per particle, as suggested by the electron densities seen in TEM. The size of the ELP particles was influenced by sample concentration, with higher concentrations associated with larger particles and, in some cases, micron-scale aggregate formation and precipitation. More concentrated samples also showed more dynamic diameters upon heating, with samples at 1.0 mg/mL showing significant decreases in diameter with heating. Chain length also played a role, with shorter chain lengths resulting in larger particles overall and greater tendencies for precipitation. ELP precipitation was observed for two separate constructs and potentially influenced by both guest amino acid hydrophobicity and chain length. More hydrophobic guest amino acids may allow for greater stability for shorter ELP sequences and may also result in a less reversible particle formation and/or precipitation depending on sample concentration. Hysteresis was observed in all samples and, due to its relationship with the Tt, varied with ELP concentration. Additionally, hysteresis was found to be more pronounced overall for constructs with shorter chain lengths. These short ELPs also were not found to disassemble as reliably as their longer counterparts, with sample concentration also influencing measurable resolubilization. Hysteresis has been sparingly observed in other ELP systems, with constructs composed of elastin exons 20–24 or of crosslinked valine-containing ELP microgels both exhibiting minor hysteresis (< Δ10 °C) behaviour [28, 40]. A pronounced ~ 15 °C hysteresis was observed for a VPAVG-derived ELP at 32.1 mg/mL, with structural studies revealing that the additional methyl group on the third amino acid caused less bound water to be associated with the protein when heated above its transition temperature which stabilized the particles and impeded their redissolution [41–43]. It is possible that a similar mechanism is responsible for the hysteresis observed for some leucine-containing ELPs reported herein, as these constructs also contain an additional methyl group and result in a more hydrophobic sequence overall, though further study would be required to demonstrate this. This mechanism may also be responsible for the irreversible assembly observed herein, as a pronounced 15–20 °C hysteresis alongside low temperature heating transition temperatures may have resulted in disassembly transition temperature below the freezing point of water and the operating temperature of the DLS instrument. Novel dilution stability testing suggested that pre-formed ELP particles composed of longer chain lengths were more stable when subjected to isothermal and isotonic dilution. Guest amino acid chemistry may also affect dilution stability with more hydrophobic residues showing smaller variations in diameter.
The roles of temperature and concentration on ELP behaviour have not been systematically analyzed and the results reported herein, in addition to the design guidelines presented above, suggest that existing ELP constructs may be used to form particles of varying diameters, depending upon solution conditions and temperature treatments. This may be a resourceful and cost-effective way of expanding upon the utility of individual ELP constructs without resorting to further sequence modifications.
In this study, leucine-containing ELPs composed of 20, 40, 80 or 160 repeats of the VPGLG sequence as well as a 40 repeat valine-containing construct were evaluated for their assembly, disassembly, particle size, charge and dilution stability characteristics. These experiments were performed at four distinct concentrations in order to deconvolute the role of sample concentration. Additional analysis allowed for the elucidation of the roles of guest amino acid chemistry and chain length on ELP behaviours.
Leucine-containing ELPs showed assembly transition temperatures dependent upon sample concentration and chain length consistent with other more hydrophilic constructs studied in the literature. Chain length was found to have an inverse relationship with particle diameter, with L20, the shortest construct, forming micron-scale aggregates and precipitating out of solution at high concentrations. This behaviour was also observed for the valine-containing V40 construct despite it being twice the length of L20. The guest amino acid chemistry was found to potentially influence the zeta potential, with more hydrophobic constructs showing greater charge and electron densities suggesting a corresponding effect on packing density. Temperature-mediated disassembly behaviour was also found to vary with chain length whereby the shortest constructs tended to resist disassembly upon cooling as low as 5 °C. L40 demonstrated that sample concentration also played a role in disassembly resistance, as more concentrated samples did not completely resolubilize, while less concentrated samples did fully disassemble. No resistance to disassembly was observed in the valine-containing construct. Dilution-mediated disassembly testing indicated that pre-formed ELP particles could be subjected to isothermal and isotonic dilution up to 20-fold their original concentration.
MSB and LDU contributed to the conception of the study. MSB, AKA and SVE contributed to the development, analysis and execution of the experiments. The manuscript was written through contributions of all authors. All authors read and approved the final manuscript.
The authors would like to acknowledge the technical assistance provided by Lavina Hsiao Wei Ng and Owais Khalid for dynamic light scattering, as well as Woo Jung Cho and the Cell Imaging Center at the University of Alberta for equipment access, training and technical expertise.
The authors declare that they have no competing interests.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Consent for publication
Ethics approval and consent to participate
This work was supported by the Natural Sciences and Engineering Research Council of Canada Discovery Grant #RES0011279. MSB was supported by Alberta Innovates Technology Futures Graduate Student Scholarship in Nanotechnology #200801440. AKA was the recipient of the Ministry of Higher Education and King Saud University Scholarship, Saudi Arabia. SVE was the recipient of a Natural Sciences and Engineering Research Council of Canada Undergraduate Student Research Award. Funding bodies did not play any role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
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