Patent Application
20150202651
The present invention is directed to a method of forming recombinant spider silk protein films and more particularly, the present invention is directed to methodology for synthesizing the film and uses of the film in various industries.
The use of recombinant spider silk proteins is well recognized in the art and has been set forth in U.S. Pat. No. 7,056,023, issued Jun. 6, 2006, to Islam et al., the contents of which is incorporated herein by reference. Generally, the disclosure explains methods and apparatuses for spinning silk protein fibers from recombinant proteins. The methods are primarily useful for spinning fibers of spider silk or silkworm silk proteins from recombinant mammalian cells and may be used to spin such fibers for use in the manufacture of industrial and commercial products.
Further examples of advancements in the art include that which is taught in U.S. Pat. No. 7,754,851, issued Jul. 13, 2010. In this reference, Scheibel et al. explain spider silk proteins, nucleic acids, coding for these recombinant spider silk proteins, as well as hosts suitable for expressing those nucleic acids. Further, there are discussions centred on a method of aggregation of spider silk proteins and the use of the proteins in the field of biotechnology and/or medicine and other industrial fields, particularly in the manufacture of automotive parts, in the aircraft construction, in the processing of textiles and leather, as well as in the manufacture and processing of paper. In United States Patent Application Publication US 2009/0263430, published Oct. 22, 2009, Scheibel et al., discuss a method of forming multilayer silk protein films and a multilayer film obtained therefrom. Various materials, products and compositions containing the multilayer film are also taught as well as the use of the film in several applications.
Other examples of the progress in this area of technology include developments evinced in U.S. Pat. Nos. 7,521,228; 5,989,894; 7,521,228; 5,989,894; 5,733,771; 5,756,677; 5,733,771; 5,756,677; 5,994,099 and 7,723,109 inter alia.
One object of one embodiment of the present invention is to provide an improved recombinant spider silk protein film.
Another object of one embodiment of the present invention is to provide a new protocol for forming a recombinant spider silk protein film.
A still further object of one embodiment of the present invention ids to provide a method of forming silk protein film comprising the steps of:
Another object of one embodiment of the present invention is to provide a method of forming silk protein film comprising the steps of:
A still further object of one embodiment of the present invention is to provide a method for modifying mechanical property of a recombinant spider silk protein film, comprising:
A further object of one embodiment of the present invention is to provide a method for modifying mechanical property of a recombinant spider silk protein film, comprising:
Another object of the present invention is to provide a method for modifying mechanical property of a recombinant spider silk protein film, comprising:
These objects are solved by the subject-matter of the independent claims. Preferred embodiments are set forth in the dependent claims.
Having thus generally described the invention, reference will now be made to the accompanying drawings, illustrating preferred embodiments.
Similar numerals employed in the drawings denote similar elements.
Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.
The importance of spider silk for industrial applications cannot be overstated. It has ubiquitous utility in the processing of paper, cosmetics, food, electronic devices, drug delivery and in the automotive industry particularly for airbags and tires. Airbags, as is well known, are designed to push the passenger back into the seat without absorbing the full impact of the force. Employing spider silk in airbags, would provide more flexibility and absorb more energy. This could make airbags a more effective lifesaver.
In respect of tires, currently, tires have Kevlar cords on the inside which makes the tires strong and reliable. The problem with Kevlar it that it has a tendency to blow up, that is the reason why tires explode. Fibers made with spider silk in the tires would allow the tire to absorb more impact, making explosions unlikely.
Particularly convenient is the fact that the film can be combined with a innumerable examples of substrates such as a cosmetic composition, a pharmaceutical or medical composition, drug delivery system, artificial cell, contact lens coating, sustained-release drug delivery system, artificial skin graft; food composition; automotive part; aeronautic component; computer or data storage device, building material, textile, filter material, membrane material, nanomaterial, electronic component and combinations thereof.
With the degree of activity in this area of technology and despite the voluminous amount of prior art that has been created, there still exists a need for expedient protocols for recombinant spider silk protein film synthesis for use in a wide variety of industries as well as a film synthesized in accordance with the protocols having superior mechanical properties. This would lead to use of the synthesized film material into the automotive, pharmacological, medical, manufacturing, food, clothing, electronics, inter alia.
Advantageously, the present invention in its many facets now presents an elegant synthesis protocol and product to address the void in this technology area.
Prior to a presentation of the synthesis of films using the spider silk protein, one possible route for the formulation of the protein is discussed below for general background.
Recombinant spider silk proteins, rSSPs, are conventionally dissolved in a very harsh organic solvent, 1,1,1,3,3,3-hexafluoroisopropanol (HFIP), to create “dopes” that can be used to create fibers, films, gels and foams. HFIP has been widely used and accepted as it is the only solvent that: 1) dissolves rSSPs at high concentrations (30% w/v) providing uniformity between various groups testing data; 2) is sufficiently volatile and miscible to be removed rapidly from the forming fiber; and 3) leaves little to no residue behind that could interfere with fiber formation. In addition, rSSPs generally are insoluble in aqueous solutions after purification, necessitating an organic solvent that meets the criteria outlined in points 1 through 3. However, there are significant problems with solvating rSSPs in HFIP or other organic solvents.
Dissolving rSSP in HFIP and then using pressure to extrude the dope into a coagulation bath does not allow the appropriate structures to form (notably fl-sheets) to an extent that the fibers or films have to be post-spin processed multiple times to achieve protein structures that result in appreciable mechanical properties. For reference purposes, Lazaris et al. discuss Spider Sik Fibers Spun from Soluble Recombinant Sik Produced in Mammalian Cells, Science 295, 472-476 (2002) (herein after “Lazaris”); and Teule et al., Modifications of spider silk sequences in an attempt to control the mechanical properties of the synthetic fibers, J. Mater Sci, 42, 8974-8985 (2007) (herein after “Teule”).
Such fiber processing methodologies include extruding the fiber into a coagulation bath that may include pure isopropanol or a mixture of isopropanol:water. The fiber may then be stretched (1.5 to 6 times) in a second bath generally containing a mixture of isopropanol and water. A third bath may also be employed that contains pure water or a majority of water, and a second stretch applied in that bath (Lazaris). Water is the recurrent theme in these baths and it is the water that converts the helical structures present due to HFIP into strength providing fl-sheets (“Teule”).
The cost of purchase and subsequent disposal of HFIP may be restrictive or prohibitive in an industrial setting of mass production. The cost to purchase HFIP is approximately $1,000/100 mls of HFIP and 100 ml of HFIP would likely be capable of solvating 20-30 g of rSSP (20-30% w/v). Water is inexpensive even in its purest form. Referencing the MSDS published on Sigma Aldrich's web-site, disposal of HFIP requires; “Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber,” a process that inherently has costs associated with it. Excess water can be evaporated or recycled and reused. Worker safety when utilizing such harsh, volatile solvents is also a consideration.
Further referring to the MSDS; “Material is extremely destructive to tissue of the mucous membranes and upper respiratory tract, eyes, and skin. Cough, Shortness of breath, Headache, Nausea” (SIC). Water has no such requirements. Finally, the process of producing rSSP products could not be considered “green” using HFIP. rSSPs are largely insoluble in water. There are a few notable exceptions: Teule describes a series of proteins (Y1S8 and A2S8) that were produced in bacteria and purified via Ni++ chromatography. Short fibers were pulled straight from the eluted, pure rSSP fraction. Lazaris describes ADF-3 (Araneus diadematus MaSp1) produced in mammalian cell culture. Water soluble ADF-3 was concentrated in the presence of glycine and extruded into a coagulation bath. A final example is a series of recombinant aciniform-like synthetic proteins that were able to be spun from an aqueous solution very similar to Teule 2007 (Xu 2012). Reference can be made to Xu et al., Recombinant Minimalist Spider Wrapping Silk Proteins Capable of Native-Like Fiber Formation. PloS-One 7(11): e50227. Doi: 10.1371/journal.pone.0050227 (2012). However, outside of this small sub-set of rSSPs, water solubility is elusive. Noteworthy is that the majority of these proteins were much smaller than the natural proteins and thus are unlikely to make mechanically useful fibers.
United States Patent Application Publication No. 2011/0230911, published Sep. 22, 2011, utilizes a top down approach using genetic manipulations and expression system manipulations to try and create water soluble silk proteins. Unfortunately, such processes are costly both in time to create the manipulations/cell lines and also the proteins appear to be expressed in mammalian cell cultures. The culture conditions for such cell lines are not only personnel and time intensive, but also the ingredients and equipment required are substantially more expensive than the more traditional bacterial expression systems. In addition, such methods are limiting as there are not that many iterations of various spider silk repeats that can be expressed in this manner that will result in a water soluble protein having appreciable mechanical properties.
To address these and other challenges, this discussion sets forth new and novel methods for solubilizing rSSPs in aqueous solutions and then creating resulting spider silk compositions therefrom. The methods and compositions described herein in embodiments create aqueous dopes from rSSPs that are otherwise not soluble in water. The methods and compositions described herein may be applied to proteins expressed by any organism, reducing the cost of production and also possibly improving the mechanical properties of the fibers, films, gels and foams by the inclusion of water in the dope.
In certain embodiments, methods of preparing aqueous dopes of rSSP may include the following steps: mixing rSSP, water, and optional additives; optionally sonicating the mixture; microwaving the mixture; and optionally centrifuging the microwaved mixture.
rSSP and water are combined to create a doping mixture of greater than about 2% w/v (e.g. 0.02 g SSpS:1 mL H2O). In embodiments, the w/v does not typically exceed 50%. However, any percentage of less than 50% may be used. Suitable rSSPs include: MaSp1 (as described in U.S. Pat. Nos. 7,521,228 and 5,989,894), MaSp2 (as described in U.S. Pat. Nos. 7,521,228 and 5,989,894), MiSp1 (as described in U.S. Pat. Nos. 5,733,771 and 5,756,677), MiSp2 (as described in U.S. Pat. Nos. 5,733,771 and 5,756,677), Flagelliform (as described in U.S. Pat. No. 5,994,099), chimeric rSSPs (as described in U.S. Pat. No. 7,723,109), Pyriform, aciniform, tubuliform, aggregate gland silk proteins, and AdF-3 and AdF-4 from Araneus diadematus. Each of the above referenced patents is herein incorporated by reference in its entirety.
Various additives may be optionally added to the mixture. Suitable additives include compositions that contribute to the solubility of the rSSP in the solution. Some additives break or weaken disulfide bonds, thereby increasing the solubility of rSSPs. Other additives also serve to prevent hydrogel formation after the completion of the microwave step, as set forth below. If the solution forms a hydrogel quickly and the desired end product is not a gel, then additives capable of delaying or inhibiting such a formation may be desirable. In some embodiments, multiple additives may be added to achieve desired end products.
For example, to combat hydrogel formation, various additives may be added to the suspension of rSSP and water prior to microwaving the suspension. In some embodiments, acid, base, free amino acids, surfactants, or combinations thereof may be employed to combat hydrogel formation. For example, additions of acid (formic acid and acetic acid alone or together at 0.1% to 10% v/v), base (ammonium hydroxide at 0.1% to 10% v/v), free amino acids (L-Arginine and L-Glutamic Acid at 1 to 100 mM) as well as a variety of surfactants (Triton X-100 at 0.1% v/v) may be used. The additions of these various chemicals not only aid the solubility of rSSP when microwaved but in certain combinations also delay the solution from turning into a hydrogel long enough for the solution to be spun into a fiber.
By altering and adjusting the combinations of additives to the dopes, the mechanical properties of the spun fiber are significantly iM Pacted. For example, too much acid or base may result in fibers that are brittle with little to no extensibility; too little acid or base may result in dopes where the rSSP will not solubilize to the extent necessary for fiber spinning or turns to a hydrogel quickly.
Exemplary additives also include compositions capable of breaking or weakening disulfide bonds, such as β-mercaptoethanol or dithiothreitol may be added to reduce bonds and increase solubility. Suitable amounts of such additives may include from about 0.1 to about 5% (v/v). In embodiments where the rSSP does not contain cysteine, the use of such additives may be unnecessary. In some embodiments employing major ampulate silk proteins 1 and 2 (MaSp1 and MaSp2, respectfully), disulfide bonds (cysteine) are present in the C-terminus of the non-repetitive regions of MaSp1 and MaSp2. These proteins are described in U.S. Pat. Nos. 7,521,228 and 5,989,894, the entirety of both being herein incorporated by reference. In addition, the C-term is present in various goat-derived spider silk proteins M4, M5 and M55 proteins, which are described in U.S. Pat. No. 7,157,615, issued Jan. 2, 2007, the entirety of which is incorporated by reference in its entirety. In some embodiments, formic acid and/or acetic acid may be included in as little as 0.3% (v/v) but even lower amounts (0.1% v/v) are possible. Additionally, it is possible to solubilize rSSP without using any additives.
Exemplary additives are set forth in Table 1 (below), where dope formulations prepared according to the methods described herein and their resultant fibers/films mechanical properties are listed.
To formulate an aqueous solution of rSSP, additives can be chosen from any of the five columns. For instance one or a combination of acids can be chosen from column one and combined with one or combinations of free amino acids from column three, as well as disulphide reducing compounds from column four and “Other” additives as required by the particular protein. Generally, it would not be useful to include both an acid from column one with a base from column two. However, a base from column two can be combined with additives from columns three and four. In some embodiments free amino acid analogues may also be used in place of or in addition to other free amino acids. For example, imidazole anaolgues such as benzimidazole, dihydroimidazole (imidazoline), pyrrole, axazole, thiazole, pyrazole, and triazoles may be used.
In some embodiments, the mixture containing water, rSSPs, and optional additives may be sonicated. The addition of sonication to the rSSP and water suspension may greatly increase the amount of solublized protein. Sonication may be performed with any suitable sonicator, such as a Misonix 3000 with microtip at 3.0 watts) either prior to microwaving, after microwaving and cooling, or both.
In embodiments, sonication may be employed to improve the amount of rSSP solubilized and, thus, reduce the amount of protein required to form an aqueous spin dope. Sonication also has the added benefit of producing a more homogenous solution. Sonication also improves and/or changes mechanical properties for rSSP composition products, particularly fiber mechanical properties.
For example, initial experiments required a 12.5% w/v MaSp1 analogue (125 mg MaSp1 into 1 ml of aqueous) in order to spin a fiber. Sonicating after microwaving reduced the concentration of MaSp1 to 5% w/v necessary to form fibers. Lower rSSP concentrations results in more fiber spun from a given amount of protein as well as finer fibers which has been demonstrated to increase the mechanical properties in other systems (electrospinning from HFIP based dope solutions (Teule).
The mixture containing water, rSSPs, and optional additives may be microwaved prior to or after the optional sonication step. In embodiments, any microwave may be employed. In some embodiments, the mixture should be sealed prior to microwaving so as to avoid evaporation.
The mixture may be microwaved for any suitable amount of time to achieve the desired end product. The time depends on the power of the microwave and the amount of solution to be microwaved. In some embodiments, the solution may be stirred or agitated during microwaving so as to evenly expose the mixture to the microwaves. Appropriate times per unit being microwaved include, for example, from 10 to 90 seconds per 1 milliter of mixture. In some embodiments the 1 ml mixture may be set at from about 10% to 100% power for from about 5 second to 120 seconds.
After microwaving, the solution is allowed to cool and/or is taken to other processing steps, depending on the desired product. In some alternative embodiments, microwaving may be replaced with a reactor, such as the Series 4590 Micro Stirred Reactor by Parr Instrument Company or a larger commercial reactor. In such embodiments, the reactor is configured to control mixing, pressure, and temperature parameters. Suitable mixing speeds, temperatures, and pressures may be exerted in such embodiments.
In some embodiments, the microwaved mixture may be optionally centrifuged. After centrifugation, the resulting supernatant may be removed and then used for rSSP compositions and further processing.
Hydrogels may be generated from aqueous rSSP solutions by allowing the solubilized rSSP to cool. Additives to the dope such as acetic or formic acid can delay the formation of the hydrogel to allow the rSSP to be transferred to a mold prior to gelation. Theoretically, the variety of shapes that can be generated is limitless. The additives to the solution will change the mechanical properties of the resulting hydrogel. Hydrogel formation has been observed in solutions with as little as 3% w/v rSSP:water and all iterations greater.
The higher the percentage of rSSP, the more rapidly the solution gelates. Work in other systems, Bombyx mori silk, has proven the phenomenon that increasing the ratio of silk to water improves the mechanical characteristics of the resulting hydrogel. As well, altering the temperature, pH and including calcium ions changes the properties of the gels (Kim, U J et al., 2004, Biomacromolecules “Structure and Properties of Silk Hydrogels” Biomacromolecules 5, 786-792).
An example of a hydrogel application is illustrated in Chao et al., “Silk Hydrogel for Cartilage Tissue Engineering.” Journal of Biomedical Materials Research Part B: Applied Biomaterials, Vol 95B, Issue 1 pg 84-90, 2010.
Aerogels may be formed by freezing and then lyopholizing a solution or hydrogel of rSSP. Theoretically, the shapes for these aerogels is also limitless as their starting hydrogels could be allowed to form in a mold and then frozen and lyophilized.
Films may be produced by pouring a dope solution onto a substrate and allowing the water and other additives to evaporate. If it is desirable to remove the film from the substrate, PDMS or Teflon allow the removal of the films. A representative dope solution comprises 50 mg/ml MaSP1 analogue, 1% formic acid, 1% acetic acid. Films may be applied as coatings or utilized after removal from a substrate. Film formation will be discussed in greater detail hereinafter.
Foam may be generated from aqueous based solvents by a variety of methods and dope conditions. One method reduced to practice is to formulate a dope solution similar/identical to that described for film generation. That solution is then placed into a vacuum chamber and a vacuum applied. The solution quickly expands and forms a foam upon curing in the chamber. Additives to the dopes such as surfactants will influence final cell size and further treatment of the foam (alcohol) are possible to also change the final properties of the foams. It is also possible that foams can be generated by chemical means, mainly peroxidase reactions, to produce CO2 that creates bubbles in the dope and upon curing a foam remains. As discussed in United States Patent Publication No. 20110230911, published on Sep. 22, 2011, Scheibel. This method is also influenced by additives such as surfactants and post formation treatments (alcohol). A final method is an extrusion method whereby the dope solution is mechanically mixed with air, or other gas, to produce foam. This method is also subject to additives and post formation treatments to alter the final foam product.
Fibers can be spun from aqueous solutions of rSSP by extrusion into a coagulation bath (alcohol) in a similar fashion as HFIP/aqueous based solutions of rSSP as described in United States Patent Application Publication No. 2005/0054830, published on Mar. 10, 2005. To summarize, the solubilized rSSP can be loaded into a syringe or other suitable extrusion instrument and then pushed through a fine bore needle into a bath comprised of isopropanol or other alcohol. As the rSSP drops through the alcohol, water is removed and a fiber is formed. That fiber can then be taken up or processed further by stretching in a second or even third bath comprised of alcohol(s), alcohol(s) and water or just water. Fibers have been formed from solutions with as little as 5% w/v solutions of rSSP:water. Similar 5% w/v solutions using HFIP as the solvent will not form fibers.
In some embodiments, it is not necessary for the solution to remain liquid to form fibers. Indeed, in some embodiments, fibers may be formed from a hydrogel. For example, when forming fibers from MaSp2 proteins, the process may be stopped, the syringe immediately removed for visualization, and a hydrogel may be observed. In contrast, forming fibers from a hydrogel with MaSp1 proteins results in deleterious effects.
It is important to note that each individual rSSP, due to its unique amino acid sequence, will have different requirements for aqueous solubility. The rSSP concentration, microwave time and power setting, amount of acid or base, and requirements for free amino acids or surfactants will be different. There does not appear to be one set of additives that achieves aqueous solubility and that also delays hydrogel formation for all rSSPs.
As an example, a 12.5% w/v solution of a MaSp1 and MaSp2 analogue can be prepared identically in terms of additives. The MaSp1 will become soluble in water easily and stay liquid for an extended period of time. The MaSp2, on the other hand, will form a hydrogel within minutes of removal from the microwave and requires more microwave time to solubilize.
All examples in this document are illustrative only and are not intended to limit the disclosure in any way.
An aqueous recombinant spider silk protein (rSSP) dope solution was prepared by weighing out the rSSP such that a mass concentration of between 1 and 40% (w/v) of protein was achieved in 1 ml of water. For example, 50 mg of protein in 1 ml of water yielded a 5% w/v solution of protein to water. The suspension of rSSP and water was sealed inside a 3 ml glass Wheaton vial using a PTFE lined cap. The suspension and vial were then placed in a conventional 1500 watt microwave and microwaved at 50% power for 30 seconds. This solubilized the protein powder in the water.
Although this method may work to solubilize the rSSP, the solution quickly formed a hydrogel upon cooling and was generally not available thereafter to spin fibers by extrusion. If the goal of generating the aqueous dope is to form films, foams, hydrogels or aerogels, this method may be acceptable. Microwave time may vary depending on the volume of the dope, rSSP used, additives chosen, and whether sonication is utilized.
The following samples were prepared, one of which was not sonicated:
Fibers spun from dopes that are not sonicated (
Thus, fiber defects when spun from aqueous dopes may be diminished by sonication of the dope.
The following examples set forth numerous rSSP sample tests and resulting data according the formulations and processing criteria set forth below:
25 mg of M5 (Nephila clavies MaSP2 analogue) was measured out using a fine balance into a 3 ml Wheaton glass vial with PTFE seal inside a plastic cap.
Included in the dope solution:
The PTFE sealed cap was placed on the 3 ml vial tightly. The solution and vial were placed into a conventional microwave (GE 1.6 kW) and microwaved for 30 seconds at 50% power. After microwaving, the solution was placed into a centrifuge (VWR Clinical 2000 set at 6,000 RPM) for 2 minutes to clarify. The supernatant is removed from any remaining pellet for spinning fibers or producing other materials such as films, gels or foams.
Fiber testing results (10 samples) for 1.5× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (9 samples) for 2.0× post spin stretch in an 80:20 isopropanol:water bath.
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 2.27 1.43 0.03
Fiber testing results (9 samples) for 2.5× post spin stretch in an 80:20 isopropanol water bath.
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 2.95 0.25 9.11 0.003
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 5.15 14.64 17.17 0.54
Fiber testing results (10 samples) for 3.0× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (10 samples) for 3.5× post spin stretch in an 80:20 isopropanol:water bath.
125 mg of M5 (Nephila clavipes MaSP2 analogue) was measured out using a fine balance into a 3 ml Wheaton glass vial with PTFE seal inside a plastic cap.
Included in the dope solution:
The PTFE sealed cap was placed on the 3 ml vial tightly. The solution and vial were placed into a conventional microwave and microwaved for 30 seconds at 50% power. After microwaving, the solution was placed into a centrifuge (VWR Clinical 2000 set at 6,000 RPM) for 2 minutes to clarify.
The supernatant was removed from any remaining pellet for spinning fibers or producing other materials such as films, gels or foams.
Fiber testing results (9 samples) 1.5× post spin stretch in an 80:20 isopropanol:water bath.
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 2.12 14.27 18.04 0.18
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 2.64 8.76 22.91 0.09
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 5.74 3.10 13.83 0.05
Fiber testing results (9 samples) 2.0× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (10 samples) 2.5× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (10 samples) 3.0× post spin stretch in an 80:20 isopropanol:water bath.
125 mg of M5 (Nephila clavipes MaSP2 analogue) was measured out using a fine balance into a 3 ml Wheaton glass vial with PTFE seal inside a plastic cap.
Included in the dope solution:
Standard deviation 5.03 2.56 20.69 0.06
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 1.08 13.71 17.87 0.18
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 2.46 26.92 18.06 0.30
The PTFE sealed cap was placed on the 3 ml vial tightly. The solution and vial were placed into a conventional microwave and microwaved for 30 seconds at 50% power. After microwaving, the solution was placed into a centrifuge (VWR Clinical 2000 set at 6,000 RPM) for 2 minutes to clarify. The supernatant was removed from any remaining pellet for spinning fibers or producing other materials such as films, gels or foams.
Fiber testing results (10 samples) 1.5× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (10 samples) 2.0× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (10 samples) 2.5× post spin stretch in an 80:20 isopropanol:water bath.
125 mg of M5 (Nephila clavipes MaSP2 analogue) was measured out using a fine balance into a 3 ml Wheaton glass vial with PTFE seal inside a plastic cap.
Included in the dope solution:
The PTFE sealed cap was placed on the 3 mi vial tightly. The solution and vial were placed into a conventional microwave and microwaved for 30 seconds at 50% power.
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 10.74 3.66 15.36 0.06
Diameter (μm) Energy to break MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 5.23 23.18 14.17 0.35
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 6.42 25.25 16.49 0.43
After microwaving, the solution was placed into a centrifuge (VWR Clinical 2000 set at 6,000 RPM) for 2 minutes to clarify. The supernatant was removed from any remaining pellet for spinning fibers or producing other materials such as films, gels or foams.
Fiber testing results (10 samples) 1.5× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (9 samples) 2.0× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (10 samples) 3.5× post spin stretch in an 80:20 isopropanol:water bath.
125 mg of M4 (Nephila clavies MaSP1 analogue) was measured out using a fine balance into a 3 ml Wheaton glass vial with PTFE seal inside a plastic cap.
Included in the dope solution:
The PTFE sealed cap was placed on the 3 ml vial tightly. The solution and vial were placed into a conventional microwave and microwaved for 30 seconds at 50% power. After microwaving, the solution was placed into a centrifuge for 5 minutes to clarify. The Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1).
Standard deviation 10.11 0.11 7.64 0.003
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 8.29 1.39 32.07 0.009
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 2.04 11.70 8.09 0.16 supernatant was removed from any remaining pellet for spinning fibers or producing other materials such as films, gels or foams.
Fiber testing results (10 samples) 1.5× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (10 samples) 2.0× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (10 samples) 2.5× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (9 samples) 3.0× post spin stretch in an 80:20 isopropanol:water bath.
125 mg of M4 (Nephila clavipes MaSP1 analogue) was measured out using a fine balance into a 3 ml Wheaton glass vial with PTFE seal inside a plastic cap.
Included in the dope solution:
Standard deviation 16.23 1.25 7.83 0.04
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 2.71 4.79 15.99 0.07
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 3.40 18.50 30.78 0.16
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 3.88 3.49 21.80 0.08
The PTFE sealed cap was placed on the 3 ml vial tightly. The solution and vial were placed into a conventional microwave and microwaved for 30 seconds The solution and vial were allowed to cool and then, the solution was sonicated using a microtip on a Misonix sonicator for 1 minute at a power setting of 1.5. The PTFE sealed cap was placed on the 3 ml vial tightly. The solution and vial were placed into a conventional microwave and microwaved for 30 seconds at 50% power. After microwaving, the solution was placed into a centrifuge for 5 minutes to clarify. The supernatant was removed from any remaining pellet for spinning fibers or producing other materials such as films, gels or foams.
Fiber testing results (8 samples) 1.5× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (9 samples) 2.0× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (10 samples) 2.5× post spin stretch in an 80:20 isopropanol:water bath.
Fiber testing results (10 samples) 3.0× post spin stretch in an 80:20 isopropanol:water bath.
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 3.32 0.14 13.03 0.002
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 2.45 0.16 3.24 0.006
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 10.08 1.96 35.24 0.04
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 2.27 0.19 13.89 0.002
50 mg (5% w/v) of M4 (Nephila clavipes MaSP1 analogue) was measured out using a fine balance into a 3 m Wheaton glass vial with PTFE seal inside a plastic cap.
Included in the dope solution:
The PTFE sealed cap was placed on the 3 ml vial tightly. The solution and vial were placed into a conventional microwave and microwaved for 30 seconds at 50% power. After microwaving and cooling for 5 minutes, the solution was sonicated for 1 minute at 3.0 watts. After microwaving, the solution was placed into a centrifuge for 2 minutes to clarify. The supernatant was removed from any remaining pellet for spinning fibers or producing other materials such as films, gels or foams.
Fiber testing results 1.5× post spin stretch in an 80:20 isopropanol:water bath.
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 0.35 0.39 8.30 0.007
Fiber testing results 3.0× post spin stretch in an 80:20 isopropanol:water bath.
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 1.15 12.92 16.81 0.12
80 mg (8% w/v) of M4 (Nephila clavies MaSP1 analogue) in addition to
20 mg (2% w/v) of M5 (Nephila clavipes MaSP2 analogue) was measured out using a fine balance into a 3 ml Wheaton glass vial with PTFE seal inside a plastic cap.
Included in the dope solution:
The PTFE sealed cap was placed on the 3 ml vial tightly. The solution and vial were placed into a conventional microwave and microwaved for 35 seconds at 50% power. After microwaving, the solution was placed into a centrifuge for 3 minutes to clarify. The supernatant was removed from any remaining pellet for spinning fibers or producing other materials such as films, gels or foams.
Fiber testing results 2.0× post spin stretch in an 80:20 isopropanol:water bath. Diameter (μm)
Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 5.59 0.42 14.59 0.003
Fiber testing results 2.5× post spin stretch in an 80:20 isopropanol:water bath.
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 1.07 3.84 10.78 0.04
Fiber testing results 3.0× post spin stretch in an 80:20 isopropanol:water bath.
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Standard deviation 1.85 17.46 6.96 0.23
Fiber testing results 3.5× post spin stretch in an 80:20 isopropanol:water bath.
Diameter (μm) Energy to break (MJm−3) Max Stress (M Pa) Max Strain (mmmm−1)
Energy to break 3.88 10.83 37.40 0.13
The methods and compositions described herein may also be applied to other traditionally insoluble proteins. Exemplary proteins that may be used in these methods include naturally occurring and synthetic proteins associated with protein misfolding diseases such as prions (CWD, BSE, vBSE, Creutzfeldt-Jakob), Alzheimer's, and Parkinson's.
Additionally, synthetically produced G-protein couple receptors (GPCR) are difficult targets as they to suffer aqueous solubility issues. Approximately 40% of drugs produced today are targeted at GPCRs. The methods described herein may also be applied to such GPCR.
Having the above as a background for possible rSSP synthesis, the discussion will now focus on the films incorporating the rSSP.
Referring initially to the drawings depicting the apparatus used in generating the films,
Typical dimensions for the C-card 10 include an overall length of 19 mm, width of 9.5 mm with a depth of the open area being 6.5 mm and a height of 8 mm. These dimensions are, of course exemplary and specific for the testing devices used. In the event that alternative testing devices are employed, then there would be a commensurate change in the dimensions noted above.
A threaded member 36 is mounted between end members 22 and 24 and extends through receiving members 32 and 34. The threaded member 36 may be actuated by manual or power assistance. In the embodiment depicted, a handle 38 is provided for manual actuation. Once rotated, at least one of the receiving members 22 and 24 moves either towards or away from the other depending on the direction of rotation of the handle 38 and thus threaded member 36.
Film samples 40 are shown mounted to the receiving members 22 and 24 and are mounted by suitable adhesive. The arrangement is effective to stretch a series of samples of film 40 consistently with equivalent force and simultaneously to ensure reproducibility in stretch results. Conveniently, owing to the portability of the arrangement 20, a sample loaded arrangement, such as that shown, may be immersed entirely in a solvent or the film exposed only (discussed herein after regarding film synthesis). Note that an automated version of this can be easily constructed from commonly available parts.
Turning now to the synthesis of the films, each water based dope formed and used in the example where noted, contained between 1% and 15% protein to which water was added together with acids, crosslinking agents, antibiotics, nanoparticles and/or surfactants depending on the protein in order to maximize solubility, increase process ability, functionalize and/or customize mechanical properties. The dope was microwaved for a period of between 10 and 60 seconds in a sealed container optionally followed by multiple steps of sonication and further microwaving to liquefy the dope and solubilize all protein. This procedure can be applied to both goat and bacterially derived spider silk protein as well as spider silk protein from any other source.
Each water based dope was made in a sealed, microwavable vial capable of holding between 3 and 10 times the volume being made to prevent explosions. The solution contained between 1% and 15% or 10-150 mg/mL of recombinant spider silk protein to which was added water, acids, imidazole, crosslinking agents, antibiotics, nanoparticles and/or surfactants depending on the desired final product in order to maximize solubility, increase processability, functionalize and/or customize mechanical properties.
Each dope contained between 80% and 100% water and thus is referred to as a water-based dope. The vial containing the dope was sealed and microwaved for a period of between 10 and 60 seconds which optionally was followed by multiple steps of sonication and further microwaving to liquefy the dope and solubilize all protein. This procedure has been applied to both goat derived spider silk protein and bacterial-derived protein.
HFIP based dopes are also made in sealed vial but may be filled to the top. The vial with the HFIP based dope is set to mix overnight on a mini labroller. The solution contains 1% and 15% or 10-150 mg/mL protein to which is added HFIP, acids, crosslinking agents, antibiotics, nanoparticles and/or surfactants depending on the desired final product in order to maximize solubility, increase processability, functionalize and/or customize mechanical properties. Each dope contains between 80% and 100% HFIP and thus is called a HFIP-based dope.
50 mg of goat generated M4 (MaSp1 in Nephila clavipes) powder was placed into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution was 1 mL Nanopure water from a Thermo Fisher brand Barnstead. The plastic lid was then tightened onto the vial in order to prevent leaking. The vial and contents were then microwaved in a 1.6 kW GE household microwave oven for 1 minute. The dope solution was then poured, 200 μL a band, onto 4 bands of Sylgard 182 slicone elastomer Polydimethylsioxane (PDMS) 5:1 base: curing agent measuring 30×7 mm and allowed to dehydrate. After drying, the film was cut to 3.5×13 mm and weighed to determine thickness. The film was then mounted on the plastic C-card, discussed supra with respect to
50 mg of M4 powder was placed into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution was 999 mL Nanopure water from a Thermo Fisher brand Barnstead; 1 μL Formic acid, ACS, 88%+ from Alfa Aesar and 1 μL Glutaraldehyde (Added after centrifugation step). The plastic lid was then tightened onto vial to prevent leaking. The vial and contents were then microwaved in a 1.6 kW GE household microwave oven for 30 seconds The solution was then sonicated for 1.5 minutes at a power setting of 3 W using a Misonix sonictor 3000 with a microtip. The vial and contents were then microwaved in a 1.6 kW GE household microwave oven for 30 seconds. The solution was then sonicated for 1.5 minutes at a power setting of 3 W using a Misonix sonictor 3000 with a microtip. The vial and contents were then microwaved in a 1.6 kW GE household microwave oven for 30 seconds. The vial was then placed in a VWR 50 mL centrifuge tube with a 2 Kimwipes at the bottom for cushion. The centrifuge tube and contents were then placed in a VWR Clinical 200 centrifuge with a balance tube on the other side and centrifuged for 1 minute at 6000 RPM. Glutaraldehyde was then added to the vial and gently shaken to form a homogeneous mixture.
The dope solution was then poured with 200 μL per band onto 4 bands of Sylgard 182 silicone elastomer Polydimethylsiloxane (PDMS) 5:1 base: curing agent measuring 30×7 mm and allowed to dehydrate. After the drying stage, the film was prepared and tested as noted in the previous examples. The X-ray diffraction pattern is shown in
50 mg of M4 powder was introduced into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution was 999 mL Nanopure water from a Thermo Fisher brand Barnstead; 1 μL Formic acid, ACS, 88%+ from Alfa Aesar and 1 μL Glutaraldehyde (Added after centrifugation step). The plastic lid was then tightened onto vial to prevent leaking. The vial and contents were then microwaved as previous examples have delineated.
The solution was sonicated for 1.5 minutes at a power setting of 3 W using a Misonix sonicator 3000 with a microtip. The vial and contents were then microwaved in a 1.6 kW GE household microwave oven for 30 seconds. The vial was then placed in a VWR 50 mL centrifuge tube with a 2 Kimwipes at the bottom for cushion. The centrifuge tube and contents were then placed in a VWR Clinical 200 centrifuge with a balance tube on the other side and centrifuged for 1 minute at 6000 RPM. Glutaraldehyde was then added to the vial and gently shaken to form a homogeneous mixture.
The dope solution was then poured with 200 μL per band, onto 4 bands of Sylgard 182 silicone elastomer Polydimethylsiloxane (PDMS) 5:1 base: curing agent measuring 30×7 mm and allowed to dehydrate. After the drying stage, the film was cut in half, length wise and glued onto the stretching device referenced in
50 mg of M4 powder was introduced into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution is 999 mL Nanopure water from a Thermo Fisher brand Barnstead; 1 μL Formic acid, ACS, 88%+ from Alfa Aesar and 1 μL Glutaraldehyde (Added after centrifugation step). The plastic lid was then tightened onto vial to prevent leaking. The vial and contents were then microwaved in a 1.6 kW GE household microwave oven for 45 seconds. The vial was then placed in a VWR 50 mL centrifuge tube with a 2 Kimwipes at the bottom for cushion. The centrifuge tube and contents were then placed in a VWR Clinical 200 centrifuge with a balance tube on the other side and centrifuged for 1 minute at 6000 RPM. Glutaraldehyde was then added to the vial and gently shaken to form a homogeneous mixture.
The dope solution was then poured with 200 μL per band, onto 4 bands of Sylgard 182 silicone elastomer Polydimethylsiloxane (PDMS) 5:1 base: curing agent measuring 30×7 mm and allowed to dehydrate. After drying, the film was cut in half, length wise and glued onto the stretching device of
The sample was then loaded on an MTS Synergie as previously noted and tested the same way as that discussed from the previous examples.
2.5× Stretch: Energy to break (MJm−3): 30.44; Stress (M Pa): 136.66; Strain (mmmm−1): 0.25
3× Stretch: Energy to break (MJm−3): 10.47; Stress (M Pa): 91.53; Strain (mmmm−1): 0.14
3.5× Stretch: Energy to break (MJm−3): 42.52; Stress (M Pa): 165.9; Strain (mmmm−1): 0.30
50 mg of M4 powder was introduced into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution was 999 mL Nanopure water from a Thermo Fisher brand Barnstead; 1 μL Formic acid, ACS, 88%+ from Alfa Aesar; 1 μL Glutaraldehyde (Added after centrifugation step) and 100 μL gold nanoparticles (20 nm) from Ted Pella, Inc. (Added after centrifugation step). The plastic lid was then tightened onto vial to prevent leaking. The vial and contents were then microwaved in a 1.6 kW GE household microwave oven for 30 seconds. The vial was then placed in a VWR 50 mL centrifuge tube with a 2 Kimwipes at the bottom for cushioning purposes. The centrifuge tube and contents were then placed in a VWR Clinical 200 centrifuge with a balance tube on the other side and centrifuged for 1 minute at 6000 RPM. Gold nanoparticles were added to the solution. Glutaraldehyde was then added to the vial and gently shaken to form a homogeneous mixture.
The dope solution was then poured with 200 μL per band, onto 4 bands of Sylgard 182 silicone elastomer Polydimethylsiloxane (PDMS) 5:1 base: curing agent measuring 30×7 mm and allowed to dehydrate. After the drying stage, the film was cut in half, length wise and glued onto the stretching device in a similar manner to that disclosed in the previous examples. The device was then turned top side down, dipping the films into a solution of 50% Isopropanol and 50% water for 1 minute. The film was stretched from 8.5 to 29.75 mm (3.5×). After stretching, the stretching apparatus was turned right side up and the films dried with a Kimwipe. The films were then treated with steam in place for 5 minutes.
After steaming, the stretching apparatus was slackened from 29.75 to 28.5. The films were then dried with a Kimwipe and cut off the stretching device with 15 mm removed from the middle of the film. The film was then mounted on the plastic C-card as discussed previously.
The sample was then loaded on an MTS Synergie as noted previously.
Results: Energy to break (MJm−3): 7.51; Stress (M Pa): 116.74; Strain (mmmm−1): 0.08
50 mg of goat produced M4 (MaSp1 in Nephila clavipes) powder was introduced into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution was 999 mL Nanopure water from a Thermo Fisher brand Barnstead; 1 μL Formic acid, ACS, 88%+ from Alfa Aesar and 1 μL Kanamycin stock (15 mg/ml) (Added after centrifugation step). The plastic lid was then tightened onto vial to prevent leaking. The vial and contents were then microwaved in a 1.6 kW GE household microwave oven for 30 seconds.
The dope solution was then poured with 200 μL a band onto 4 bands of Sylgard 182 silicone elastomer Polydimethylsiloxane (PDMS) 5:1 base: curing agent measuring 30×7 mm and allowed to dehydrate. After drying, 7 mm discs were punched out of the films. The disc was then put onto a lawn of E. coli grown on LB agar. The result is illustrated in
50 mg of goat produced M5 (MaSp2 in Nephila clavipes) powder was placed into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution was 850 μL Nanopure water from a Thermo Fisher brand Barnstead; 50 μL Acetic acid and 100 μL 50M L-Arginine. The plastic lid was then tightened onto vial to prevent leaking. The vial and contents were then microwaved in a 1.6 kW GE household microwave oven for 15 seconds. The centrifuge tube and contents were then placed in a VWR Clinical 200 centrifuge with a balance tube on the other side and centrifuged for 1 minute at 4185 g.
The dope solution was then poured with 200 μL per band, onto 4 bands of Sylgard 182 silicone elastomer Polydimethylsiloxane (PDMS) 5:1 base: curing agent measuring 30×7 mm and allowed to dehydrate. After drying, the film is cut to 3.5×13 mm and weighed to determine thickness. The film was then mounted on the plastic C-card as noted previously.
The sample was then loaded on an MTS Synergie following similar parameters as above. The X-ray diffraction data is shown in
40 mg of goat produced M5 (MaSp2 in Nephila clavipes) powder was introduced into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution was 800 μL Nanopure water from a Thermo Fisher brand Barnstead; 0.5 μL Formic acid; 200 μL 1M Imidazole and 0.5 μL Glutaraldehyde (Added after centrifugation step). The plastic lid was then tightened onto vial to prevent leaking. The vial and contents are then microwaved in a 1.6 kW GE household microwave oven for 30 seconds. The centrifuge tube and contents were then placed in a VWR Clinical 200 centrifuge with a balance tube on the other side and centrifuged for 1 minute at 4185 g.
The dope solution was then poured with 200 μL per band, onto 4 bands of Sylgard 182 silicone elastomer Polydimethylsiloxane (PDMS) 5:1 base: curing agent measuring 30×7 mm and allowed to dehydrate. After the drying stage, the film was cut to 3.5×13 mm and weighed to determine thickness. The film was then mounted on the plastic C-card and tested as noted previously.
50 mg of E. coli produced A4S8 (derived from MaSp2 and Flagelliform in Nephila clavipes) powder into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution was 1 mL Nanopure water from a Thermo Fisher brand Barnstead and 1 μL Formic acid, ACS, 88%+ from Alfa Aesar. The plastic lid was then tightened onto vial to prevent leaking. The vial and contents were then microwaved in a 1.6 kW GE household microwave oven for 15 seconds.
The solution was then sonicated for 1.5 minutes at a power setting of 3 W using a Misonix sonictor 3000 with a microtip. The vial and contents were then microwaved in a 1.6 kW GE household microwave oven for 15 seconds. The solution was then sonicated for 1.5 minutes at a power setting of 3 W using a Misonix sonictor 3000 with a microtip. The vial and contents were then microwaved in a 1.6 kW GE household microwave oven for 20 seconds. The vial was then placed in a VWR 50 mL centrifuge tube with a 2 Kimwipes at the bottom for cushion. The centrifuge tube and contents were then placed in a VWR Clinical 200 centrifuge with a balance tube on the other side and centrifuged for 3 minutes at 4185 g.
The dope solution was then poured with 400 μL per band, onto 4 bands of Sylgard 182 silicone elastomer Polydimethylsioxane (PDMS) 5:1 base: curing agent measuring 30×7 mm and allowed to dehydrate. After the drying stage, the film was cut to 3.5×13 mm and weighed to determine thickness. The film was then mounted on the plastic C-card and tested as previously disclosed.
50 mg of goat produced M4 (MaSp1 in Nephila clavipes) powder was introduced into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution is 1 mL HFIP. The plastic lid was then tightened onto vial to prevent leaking. The vial and contents were then mixed overnight on a mini labroller.
The dope solution was then poured, 200 μL a well, into 4 wells of Sylgard 182 silicone elastomer Polydimethylsiloxane (PDMS) mold using 5:1 base: curing agent measuring 30×7×0.3 mm and allowed to dehydrate. After the drying stage, the film was cut to 3.5×13 mm and weighed to determine thickness. The film was on the plastic C-card and tested as previously noted.
50 mg of goat produced M4 (derived from MaSp1 in Nephila clavipes) powder was introduced into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution was 800 μL HFIP and 200 μL Formic acid, ACS, 88%+ from Alfa Aesar. The plastic lid was then tightened onto vial to prevent leaking. The vial and contents were then mixed overnight on a mini labroller.
The dope solution was then poured with 200 μL per well, into 4 wells of Sylgard 182 silicone elastomer Polydimethylsiloxane (PDMS) mold using 5:1 base: curing agent measuring 30×7×0.3 mm and allowed to dehydrate. After the drying stage, the film was cut to 3.5×13 mm and weighed to determine thickness. The film was then mounted on the plastic C-card and tested as previously discussed.
The X-ray diffraction pattern is shown in
50 mg of M4 (MaSp1 in Nephila clavipes) powder was introduced into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution was 1 mL HFIP and 1 μL Glutaraldehyde (Added 10 minutes before pouring films). The plastic lid was then tightened onto vial to prevent leaking. The vial and contents were then mixed overnight on a mini labroller. Gluteraldehyde was added to the vial and gently shaken to homogenize the solution.
The dope solution was then poured with 200 μL per well, into 4 wells of Sylgard 182 silicone elastomer Polydimethylsiloxane (PDMS) mold using 5:1 base: curing agent measuring 30×7×0.3 mm and allowed to dehydrate. After the drying stage, the film was cut to 3.5×13 mm and weighed to determine thickness. The film was then mounted on the plastic C-card and tested as previously discussed.
The X-ray diffraction pattern is shown in
50 mg of goat produced M4 (MaSp1 in Nephila clavipes) powder was introduced into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution was 1 mL HFIP and 1 μL Glutaraldehyde (Added 10 minutes before pouring films). The plastic lid was then tightened onto vial to prevent leaking. The vial and contents were then mixed overnight on a mini labroller. Gluteraldehyde was added to the vial and gently shaken to homogenize solution.
The dope solution was then poured with 200 μL per well, into 4 wells of Sylgard 182 silicone elastomer Polydimethylsiloxane (PDMS) 5:1 base: curing agent measuring 30×7×0.3 mm and allowed to dehydrate. After the drying stage, the excess was cut off the edges and the film cut in half, length wise and glued onto the stretching device as set forth previously.
The device was then turned top side down, dipping the films into a solution of 80% Methanol and 20% water for 30 seconds. The stretching device was then rotated top side up and the films stretched. This procedure was repeated to include separate stretches, namely (i) 8.5 to 17 mm (2×); (ii) 8.5 to 21.25 mm (2.5×) and (iii) 8.5 to 23.375 mm (2.75×). After stretching, the films were cut off of the stretching device and 15 mm removed from the middle of the film. The film was then mounted on the plastic C-card and tested as previously discussed.
The X-ray diffraction pattern is shown in
2× Stretch: Energy to break (MJm−3): 36.72; Stress (M Pa): 115.55; Strain (mmmm−1): 0.37
2.5× Stretch: Energy to break (MJm−3): 39.39; Stress (M Pa): 189.18; Strain (mmmm−1): 0.26
2.75× Stretch: Energy to break (MJm−3): 52.33; Stress (M Pa): 212.46; Strain (mmmm−1): 0.32
50 mg of M5 (MaSp2 in Nephila clavipes) powder was introduced into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution was 1 mL HFIP and 1 μL Glutaraldehyde (Added 10 minutes before pouring films). The plastic lid was then tightened onto vial to prevent leaking. The vial and contents were then mixed overnight on a mini labroller. Gluteraldehyde was added to the vial and gently shaken to homogenize the solution.
The dope solution was then poured, 200 μL a well, into 4 wells of Sylgard 182 silicone elastomer Polydimethylsiloxane (PDMS) mold using 5:1 base: curing agent measuring 30×7×0.3 mm and allowed to dehydrate. After the drying stage, the film was cut to 3.5×13 mm and weighed to determine thickness. The film was then mounted on the plastic C-card and tested as previously discussed.
The X-ray diffraction pattern is shown in
50 mg of goat produced M5 (MaSp2 in Nephila clavipes) powder was introduced into a 3 mL Wheaton glass vial with PTFE seal inside a plastic lid. Included in the dope solution was 1 mL HFIP and 1 μL Glutaraldehyde (Added 10 minutes before pouring films). The plastic lid was then tightened onto vial to prevent leaking. The vial and contents are then mixed overnight on a mini labroller. Gluteraldehyde was added to the vial and gently shaken to homogenize the solution.
The dope solution was then poured with 200 μL per well, into 4 wells of Sylgard 182 silicone elastomer Polydimethylsiloxane (PDMS) 5:1 base: curing agent measuring 30×7×0.3 mm and allowed to dehydrate. After the drying stage, the excess was removed from the edges and the film cut in half, length wise and glued onto the stretching device of
The device was then turned top side down, dipping the films into a solution of 80% Methanol and 20% water for 30 seconds. The stretching device was then rotated top side up and the films stretched. This procedure was repeated to include separate stretches, namely (i) 8.5 to 21.25 mm (2.5×) and (ii) 8.5 to 23.375 mm (2.75×). After stretching, the films were cut off of the stretching device and 15 mm removed from the middle of the film. The film was then mounted on the plastic C-card and tested as previously discussed.
2.5× Stretch: Energy to break (MJm−3): 33.36; Stress (M Pa): 132.17; Strain (mmmm−1): 0.33
2.75× Stretch: Energy to break (MJm−3): 16; Stress (M Pa): 117.87; Strain (mmmm−1): 0.17
In conclusion, it can be seen that the protocol results in very significant increases in desirable mechanical properties in the film product completely capable of full integration into the vast industries discussed herein. As is further evident from the data presented herein, stretching of the films results in increased beta sheet with orientation in direction of the stretch. This attribute explains the substantial increase in the strength of the films.
Although the embodiments of the invention have been described above, it is limited thereto and it will be apparent to those skilled in the art that numerous modifications from part of the present invention insofar as they do not depart from the spirit, nature and scope of the described invention.
This application claims priority to U.S. Provisional Patent Application No. 61/917,259, filed Dec. 17, 2013, the entirety of which is herein incorporated by reference. This application is related to U.S. patent application Ser. No. 14/459,244, filed Aug. 13, 2014, the entirety of which is herein incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| 61917259 | Dec 2013 | US |
