Name: forming giant-sized polymersomes using gel-assisted rehydration
Uploaded: 2016-05-26T15:00:00.000+00:00
Duration: 8 min 45 s
Description: Watch this Scientific Journal Video about Forming Giant-sized Polymersomes Using Gel-assisted Rehydration at JoVE.com

We would like to gratefully acknowledge Dr. Ian M. Henderson, Andrew Gomez and Dr. Walter F. Paxton for their technical expertise, advice and help in this work. This work was supported by the U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering (BES-MSE). ACG, DYS and GDB were supported by BES-MSE. This work was performed, in part, at the Center for Integrated Nanotechnologies, an Office of Science User Facility operated for the U.S. Department of Energy (DOE) Office of Science (user project number RA2015A0004, PI: ACG).

1. Polymer and Agarose Preparation
Note: Gloves and a lab coat should be worn at all times throughout this protocol. Safety goggles are likewise required during work with any organic solvent or any step with possible splashing.&#160;
<ol>
	<li>Prepare a 5 mg/ml solution of polymer in chloroform. Add 1 ml of chloroform to 5 mg of solid poly(ethylene oxide)-b-poly(butadiene) (PEO-PBD, EO22-BD37) diblock copolymer in a glass vial and swirl to fully dissolve. Perform all steps using chloroform in a chemical fume hood.</li>
	<li>Mix in a fluorescently labeled lipid (purchased already dissolved in chloroform) at a 0.5 mol % final concentration in 99.5 mol % unlabeled polymer.
	<ol>
		<li>For example, pipette ~12 &#181;l of a 1 mg/ml fluorescently labeled lipid in chloroform into 997.58 &#181;l PEO-PBD, EO22-BD37 polymer in chloroform (with a molecular weight of 2,950 Daltons) for a final concentration of 0.5 mol % labeled lipid mixed and 99.5 mol % polymer.</li>
		<li>Store solution in an airtight vial with a chloroform-resistant lid at -20 &#176;C. Wrap plumbers tape on vial edge where the lid screws onto the vial and secure the lid on the vial. Wrap another piece of plumbers tape on the outside of the lid and finally wrap Parafilm on the outside of the tape to ensure minimal evaporation.</li>
	</ol>
	</li>
	<li>Make a 1% w/v agarose solution by mixing 0.5 mg standard agarose in 50 ml water (or 50 ml 100 mM sucrose) in a 250 ml Erlenmeyer flask. Boil the agarose solution in a standard microwave for ~1 min (or until fully dissolved as noted by the clearing of the solution). 
	Note: The agarose solution can be used after a few minutes of cooling or allowed to solidify, stored and re-melted using the same procedure.</li>
</ol>
2. Agarose Film Preparation
<ol>
	<li>Cut the end off of a 1,000 &#181;l pipette tip to prevent clogging. Using the cut tip, pipette 300 &#181;l of melted agarose solution onto a 25 mm square glass coverslip directly from the manufacturer.</li>
	<li>Allow the agarose to cool to ~65-75 &#176;C prior to deposition. If the agarose is too cool, it will begin to clump on the surface during the spreading process. Conversely, if the agarose is too hot, it will require more spreading to adhere the agarose to the surface.</li>
	<li>Hold just the edge of the coverslip with gloved fingers and use the long edge of another 1,000 &#181;l pipette tip to spread the agarose evenly across the surface of the coverslip. Move the pipette tip back and forth across the coverslip until the agarose completely adheres to and covers the coverslip.</li>
	<li>Place the agarose-coated coverslip onto a piece of Parafilm with the agarose facing up. Once the desired number of coverslips are coated, place the Parafilm with the coverslips into a 37 &#176;C incubator to dehydrate the agarose onto the surface for at least 1 hr. 
	Note: Dehydration is determined by the disappearance of the visible layer of agarose; the coverslip should look flat and clear. Once the films are fully dehydrated, store coverslips with the agarose surface facing up in a disposable plastic Petri dish.</li>
</ol>
3. Polymer Film Formation
<ol>
	<li>Pipette 30 &#181;l prepared polymer solution onto the agarose film.</li>
	<li>Hold just the edge of the coverslip with gloved fingers and use the long edge of an 18 G needle to spread the solution across the agarose films using a circular spreading motion. Continue spreading until the solution is evaporated. 
	Note: Be careful of the sharp end of the needle.</li>
	<li>Place the polymer films in a plastic Petri dish polymer side facing up and put the Petri dish into a standard house vacuum desiccator covered in aluminum foil (to prevent photobleaching of the labeled lipid) for at least 1 hr to fully remove any residual solvent.</li>
</ol>
4. Formation of Polymersomes
<ol>
	<li>Adhere a coverwell, either a home-made polydimethylsiloxane (PDMS) well (an ~0.5 cm thick block of cured PDMS with ~1 cm diameter of the middle punched out) or a commercially available well to the coverslip coated with the polymer film. Press the coverwell gently onto the polymer-coated coverslip with the polymer facing up until a tight seal is formed between the coverwell and the coverslip. Be careful not to press too hard and break the coverslip.</li>
	<li>Add 200-500 &#181;l rehydration solution (water is fine, but an array of buffers or medias also works) to the chamber (rehydration volume depends on the size of the coverwell adhered).</li>
	<li>Create a humidity chamber to decrease evaporation of the rehydration solution. Place a rolled, wet Kimwipe along the edges of a glass Petri dish. Place the polymer film with the adhered coverwell into the humidity chamber and cover with a lid. Cover the Petri dish with aluminum foil to minimize photobleaching. Place the Petri dish onto a hot plate set to 40 &#176;C for at least 30 min.</li>
	<li>Adjust the temperature of the hot plate during rehydration from 24-70 &#176;C to tune the size of the vesicles formed (Figure 5). 70 &#176;C is near the Tm of the agarose so caution should be used when proceeding beyond this temperature.</li>
</ol>
5. Characterization of Polymersomes by Fluorescence Recovery after Photobleaching (FRAP)
<ol>
	<li>Move the coverslip with the adhered coverwell directly to an inverted microscope for imaging.</li>
	<li>Choose the appropriate filter set based upon the fluorescent lipid included in the polymer solution. For Rhodamine-labeled lipids doped into the polymer solutions, use a 560/25 nm excitation filter and a 607/36 nm emission filter, or comparable filter sets.</li>
	<li>Use a 100X oil objective to focus on the top surface of the coverslip where the polymersomes will be adhered. If the polymersomes are especially large (&#62;20 &#181;m) or if the polymer film is too thick, a lower power objective (e.g., 40X) should be used to better visualize the polymersomes.</li>
	<li>Identify the polymersomes using fluorescence microscopy. Identify polymersomes by the characteristic hollow, spherical vesicle with a diameter &#62;5 &#181;m.</li>
	<li>Characterize membrane fluidity using fluorescence recovery after photobleaching (FRAP) on a fluorescence microscope containing an adjustable condenser. Due to the adherent nature and tight packing of polymersomes on the substrates, natural motion of the polymersomes is limited, increasing FRAP imaging quality.
	<ol>
		<li>Focus the microscope on the polymersome of interest. Close the condenser to a small region and ensure that the edge of a polymersome is within the imaging region of interest.</li>
		<li>Increase the camera exposure and ensure all neutral density filters are removed to effectively photobleach the region of interest. Allow the membrane fluorescence intensity to photobleach for 30-60 sec or until the fluorescence intensity is significantly decreased.</li>
		<li>Turn off the lamp and fully open the condenser. Decrease the exposure back to the starting settings and begin immediately capturing images every 30 sec for 3 min.</li>
		<li>Calculate membrane diffusion coefficients using standard methods12. If the bleached region regains fluorescence intensity within the 3-5 min, this indicates that the membrane is fluid.</li>
	</ol>
	</li>
</ol>
6. Characterization of Polymersome Size
<img alt="Figure 6" src="/files/ftp_upload/54051/54051fig6.jpg" /> 
Figure 6. Process for the size analysis of polymersomes using imaging software. Step-by-step instructions on how to measure the diameter of the vesicles formed. User must know the calibration units in pixels/&#181;m of the microscope used. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/54051/54051fig6large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<ol>
	<li>Open the acquired images of polymersomes in image analysis software13.</li>
	<li>Set the scale for the image by clicking on the analyze drop down box and the clicking &#34;set scale&#34;.
	<ol>
		<li>Calibrate the scale for the microscope using standard methods (i.e., a micrometer).</li>
		<li>Fill in the calibration units and click &#34;ok&#34;.</li>
	</ol>
	</li>
	<li>Click on the line tool box and draw a line spanning the diameter of a vesicle.</li>
	<li>Collect the length measurements by clicking on the analyze drop down box and clicking &#34;measure&#34;.</li>
	<li>Continue measuring individual vesicles following the above procedure and each new measurement will be added to the measurements data window.</li>
	<li>Press &#34;Ctrl + D&#34; after drawing each line and measuring the length to imprint the line drawn onto the image making it easier to track which vesicles have been analyzed.</li>
</ol>

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E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Molecular+weight+dependence+of+polymersome+membrane+structure,+elasticity,+and+stability.">Molecular weight dependence of polymersome membrane structure, elasticity, and stability.</a> Macromolecules. 35 (21), 8203-8208 (2002).</li><li>Amos, R. C., Nazemi, A., Bonduelle, C. V., Gillies, E. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Tuning+polymersome+surfaces:+functionalization+with+dendritic+groups.">Tuning polymersome surfaces: functionalization with dendritic groups.</a> Soft Matter. 8 (21), 5947-5958 (2012).</li><li>Egli, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Biocompatible+functionalization+of+polymersome+surfaces:+A+new+approach+to+surface+immobilization+and+cell+targeting+using+polymersomes.">Biocompatible functionalization of polymersome surfaces: A new approach to surface immobilization and cell targeting using polymersomes.</a> J. Am. Chem. Soc. 133 (12), 4476-4483 (2011).</li><li>Kim, K. T., Cornelissen, J. J. L. M., Nolte, R. J. M., Van Hest, J. C. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+polymersome+nanoreactor+with+controllable+permeability+induced+by+stimuli-responsive+block+copolymers.">A polymersome nanoreactor with controllable permeability induced by stimuli-responsive block copolymers.</a> Adv. Mater. 21 (27), 2787-2791 (2009).</li><li>Paxton, W. F., Price, D., Richardson, N. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Hydroxide+ion+flux+and+pH-gradient+driven+ester+hydrolysis+in+polymer+vesicle+reactors.">Hydroxide ion flux and pH-gradient driven ester hydrolysis in polymer vesicle reactors.</a> Soft Matter. 9, 11295-11302 (2013).</li><li>Henderson, I. M., Paxton, W. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Salt,+shake,+fuse+-+Giant+hybrid+polymer/lipid+vesicles+through+mechanically+activated+fusion.">Salt, shake, fuse - Giant hybrid polymer/lipid vesicles through mechanically activated fusion.</a> Angew. Chem. Int. Ed. 53 (13), 3372-3376 (2014).</li><li>Discher, B. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Polymersomes:+Tough+Vesicles+Made+from+Diblock+Copolymers.">Polymersomes: Tough Vesicles Made from Diblock Copolymers.</a> Science. 284 (5417), 1143-1146 (1999).</li><li>Howse, J. R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Templated+formation+of+giant+polymer+vesicles+with+controlled+size+distributions.">Templated formation of giant polymer vesicles with controlled size distributions.</a> Nat Mat. 8 (6), 507-511 (2009).</li><li>Horger, K. S., Estes, D. J., Capone, R., Mayer, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Films+of+Agarose+Enable+Rapid+Formation+of+Giant+Liposomes+in+Solutions+of+Physiologic+Ionic+Strength+Films+of+Agarose+Enable+Rapid+Formation+of+Giant+Liposomes+in+Solutions+of+Physiologic+Ionic+Strength.">Films of Agarose Enable Rapid Formation of Giant Liposomes in Solutions of Physiologic Ionic Strength Films of Agarose Enable Rapid Formation of Giant Liposomes in Solutions of Physiologic Ionic Strength.</a> J. Am. Chem. 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Sandia National Laboratories is a multi-program laboratory managed and operated by Sandia Corporation, a wholly owned subsidiary of Lockheed Martin Corporation, for the U.S. Department of Energy's National Nuclear Security Administration under contract DE-AC04-94AL85000.

Polymersomes are becoming widely explored as biological membrane mimics. The robust and versatile properties of polymers make them widely attractive for studies requiring membrane functionalization, longevity and tuned responsiveness. Traditional methods for forming giant-sized polymersomes9,10 (&#62;4 &#181;m) are labor-intensive and require expensive and specialized equipment. Here, we present for the first time, a rapid, versatile and robust method for forming giant sized polymersomes using standard inexpensive laboratory reagents and equipment.
Using gel-assisted rehydration, unilamellar polymersomes can be formed rapidly (&#60;30 min), in a variety of rehydration solutions (including cell culture media) and with a variety of different polymers (data not shown). The formation of multilamellar or asymmetric vesicles was not observed using this technique. Throughout this work, we used poly(ethylene oxide)-b-poly(butadiene) (PEO-PBD, EO22-BD37) neutral diblock copolymer. Many different polymer compositions (including charged diblock copolymers) work well using this method (not shown). However, some commercially available triblock copolymers and higher molecular weight diblock copolymers (~ &#62;5,000 Daltons) do not form distinct polymersomes. For all of the experiments in this manuscript, a low concentration of labeled lipid was doped into the polymer solutions for visualization purposes only. Other methods for visualization, including polymers directly functionalized with a fluorescent dye can also be used. Polymersomes can likewise be imaged with bright field microscopy, though fluorescence microscopy provides greater resolution.
Most minor modifications to the protocol typically do not alter results. For instance, small differences in concentration of the polymer solution spread onto the coverslips do not alter the formation of the polymer film formed. While the complete concentration range was not determined, polymersome formation will successfully occur with a large range of polymer film concentrations (e.g., 1-10 mg/ml). However, there are some protocol alterations that do negatively affect polymersome formation. The most notable is that round glass coverslips (instead of square) result in very poor formation of polymersomes. We attribute this to the extremely even coat of agarose on the glass which actually hinders the formation of polymersomes.
One of the most notable challenges of this technique is the ability to recover the polymersomes from the surface with a high yield. There are certain instances in which removing the polymersomes from the original surface can be advantageous. Due to the high background fluorescence from the dehydrated polymer film, removing individual polymersomes and adhering them to clean coverslips will increase imaging quality and characterization (particularly during FRAP analysis). To do this, gentle pipetting with a pipette tip in which the end has been cut off will desorb the polymersomes from the surface (though the number of vesicles recovered is significantly lower than those originally formed). Polymersomes can then be placed on modified coverslip surfaces, allowing the polymersome to interact with the new coverslip. Typically, for neutral PEO-PBD polymersomes, coverslips treated with ozone for 15 min allow the polymersomes to fall down to the surface for imaging. Different surface modification is required for different polymersome compositions (e.g., negatively or positively charged polymers).
Most materials used in this protocol are successfully stored and used for days to weeks. The solidified agarose can be reboiled and reused until the agarose begins to have aggregates even after boiling, or the solidified agarose begins to dry. Coverslips with dried agarose films can be stored and used indefinitely (e.g., months). The polymer dissolved in chloroform can be stored at -20 &#176;C for several months. Once the polymer film is dried on the agarose films, however, the films need to be stored under house vacuum and used within two weeks (longer term storage was not directly determined, but there are noticeable differences in polymersomes formed from polymer films older than two weeks).
Using the gel-assisted rehydration protocol presented here, hundreds of uniformly-shaped polymersomes are formed rapidly with just a few hours of labor using standard equipment and inexpensive laboratory reagents. Furthermore, polymersomes can be formed in a variety of physiological buffer solutions and from different polymer compositions (not shown). Minor alterations to the method do not negatively alter the formation of polymersomes, rendering gel-assisted rehydration a versatile and accessible technique to scientists with varying technical expertise.
The ability to easily create giant polymersomes on the size scale of cells is essential for building artificial cell-like systems. The ease of use and versatility of gel-assisted rehydration to make these polymersomes offers a huge advancement in the biomimetic field for the creation of robust cell-membrane mimics. For example, using this technique, strategies for encapsulation of different intracellular components, functionalization of the polymer with cell-membrane proteins and incorporation of membrane transport proteins, just to name a few, can be designed to build polymersome-based artificial cells.

Creation of synthetic cell-sized, giant unilamellar vesicles (GUVs) is of increasing interest in the in vitro reconstruction of different cellular processes to build a framework for the generation of an artificial cell-like system1,2. While GUVs composed of lipid membranes are excellent mimics of natural, biological membranes, they are unstable against environmental fluctuations and have a fairly short shelf life. Due to these limitations, amphiphilic block copolymers have been used as lipid mimics to form polymer vesicles, or polymersomes. Within this context, polymersomes are advantageous in the development of biomimetic cell systems due to their increased stability3, chemical versatility4,5 and modifiable physical traits6-8.
Current methods to form giant-sized polymersomes include electroformation9 and templated rehydration10, both of which are time-consuming, labor-intensive, require specialized equipment and produce low yields of intact giant polymersomes. A simple gel-assisted rehydration method was recently developed for the production of lipid GUVs11. Here, we describe an adaptation of the gel-assisted rehydration technique to create giant polymersomes with varying polymer compositions, controlled size, and in various buffer compositions.
Briefly, 1% w/v standard DNA gel electrophoresis agarose films are dehydrated onto a glass coverslip. Polymer solutions prepared in chloroform are then spread across the dehydrated agarose film and allowed to evaporate. Following complete solvent removal, polymer films are rehydrated in the buffer of choice with moderate heating (40-70 &#176;C) and giant (&#62;4 &#181;m) sized polymersomes are formed within 30 min. This method rapidly produces hundreds of fully intact, well-formed polymersomes using standard laboratory equipment and reagents at minimal costs.
<img alt="Figure 1" src="/files/ftp_upload/54051/54051fig1.jpg" /> 
Figure 1. Schematic depicting the gel-assisted rehydration method. Giant polymersomes composed of a diblock copolymer are formed after ~30 min of rehydration. The hydrophilic block is denoted in magenta and the hydrophobic block is denoted in green. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/54051/54051fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

<table><tbody><tr><td>125 ml Erlenmeyer flask</td><td>VWR</td><td>89000-360</td><td></td></tr><tr><td>18 guage needle</td><td>VWR</td><td>BD-305196</td><td></td></tr><tr><td>25 mm square coverslips</td><td>VWR</td><td>48366-089</td><td></td></tr><tr><td>Agarose</td><td>Sigma</td><td>A9539</td><td>A standard agarose for DNA gel electrophoresis</td></tr><tr><td>Chloroform</td><td>Sigma</td><td>288306-2L</td><td></td></tr><tr><td>Commerical coverwell</td><td>Electron Microscopy Sciences</td><td>70336</td><td>Press-to-Seal Silicone Isolators</td></tr><tr><td>Fiji Image Analysis Software</td><td>ImageJ</td><td></td><td>Free Download: http://fiji.sc/Fiji&amp;nbsp;&amp;nbsp;</td></tr><tr><td>Glass vial with Teflon Lid</td><td>VWR</td><td>66009-556</td><td>1.9 ml capacity, case of 144</td></tr><tr><td>Liss-rhodamine B PE Lipid</td><td>Avanti Polar Lipids</td><td>810150C</td><td>1 mg of lipid at 1 mg/ml concentration in chloroform</td></tr><tr><td>Parafilm</td><td>VWR</td><td>52858-000</td><td>10.2 cm x 38.1 m</td></tr><tr><td>poly(ethylene oxide)-b-poly(butadiene) or PEO-PBD (with a molecular weight of 2,940)</td><td>Polymer Source</td><td>P2904-BdEO</td><td>&lt;a href=&quot;http://polymersource.com/dataSheet/P2904-BdEO.pdf&quot;&gt;http://polymersource.com/dataSheet/P2904-BdEO.pdf&lt;/a&gt;</td></tr><tr><td>Pastic Petri Dish</td><td>VWR</td><td>25384-092</td><td></td></tr><tr><td>Teflon tape</td><td>VWR</td><td>300001-057</td><td>1/2&quot; width</td></tr></tbody></table>

forming giant-sized polymersomes using gel-assisted rehydration

Polymer vesicles, or polymersomes, are being widely explored as synthetic analogs of lipid vesicles based on their stability, robustness, barrier properties, chemical versatility and tunable physical characteristics. Typical methods used to prepare giant-sized (&gt; 4 &#181;m) vesicles, however, are both time and labor intensive, yielding low numbers of intact polymersomes. Here, we present for the first time the use of gel-assisted rehydration for the rapid and high-yielding formation of giant (&gt;4 &#181;m) polymer vesicles (polymersomes). Using this method, polymersomes can be formed from a wide array of rehydration solutions including several different physiologically-compatible buffers and full cell culture media, making them readily useful for biomimicry studies. This technique is also capable of reliably producing polymersomes from different polymer compositions with far better yields and much less difficulty than traditional methods. Polymersome size is readily tunable by altering temperature during rehydration or adding membrane fluidizers to the polymer membrane, generating giant-sized polymersomes (&gt;100 &#181;m).

Polymersomes were formed using the procedure outlined above (Figure 1) and the common laboratory equipment shown in Figure 2. Polymersomes were rehydrated with deionized water (Figure 3) and imaged on an inverted microscope in epifluorescence using a 100X oil objective. Note that if polymersomes are not visible, they might have formed at sizes too large to capture with a 100X oil objective; a lower power objective may need to be used instead. One of the advantages of using gel-assisted rehydration is the versatility of forming polymersomes in a variety of rehydration solutions. Polymersomes were successfully formed in deionized water, a full mammalian cell culture medium, sucrose solutions and two physiologically relevant buffer solutions (phosphate-buffered saline (PBS) or Tris-buffered saline (TBS)), as shown in Figure 4. Under standard conditions (rehydration with water at 40 &#176;C for 1 hr), greater than ~70 polymersomes are typically found per 40 x 40 &#181;m2 field of view. While the surface production of polymersomes is not homogenous, there are dozens of fields of view with this representative yield. Furthermore, polymersomes were stable in solution for at least 24 hr.
Polymersomes size was easily tuned by rehydrating polymer films at varying temperatures. Polymersomes formed in deionized water at RT had an average diameter of 2.9 &#177; 0.7 &#181;m. As the temperature increases during rehydration, the average size of the polymersomes also increases (Table 1). At high temperatures (&#62; 60 &#176;C), polymersomes formed with sizes even greater than 100 &#181;m (Figure 5).
All image processing was completed using open-source imaging software (Figure 6). Images collected were opened in the software program. The calibrated pixel size was entered into set scale box. Using the line tool, lines were drawn across the diameters. After each individual line was drawn, the calibrated length was measured and added to the results box. Data can then be plotted in the mathematical software of choice (e.g., Excel, Prism, Origin, etc.)
<img alt="Figure 2" src="/files/ftp_upload/54051/54051fig2.jpg" /> 
Figure 2. Picture of the common and inexpensive lab materials required for the formation of polymersomes. The items required are: Parafilm, an 18.5 G needle, polymer in chloroform or other appropriate solvent, a 1,000 &#181;l pipette tip, an Erlenmeyer flask, tweezers, agarose, 25 mm square coverslips, PDMS imaging wells and a glass Petri dish. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/54051/54051fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" src="/files/ftp_upload/54051/54051fig3.jpg" /> 
Figure 3. Pictures of the gel-assisted rehydration method. Dissolved agarose is spread on a 25 mm square coverslip until an even film coats the entire coverslip. Coverslips are then put into a 37 &#176;C incubator and film is dehydrated. A polymer solution is deposited onto the dehydrated agarose film and spread using a needle in a circular motion. The coverslip is then place in a desiccator O/N to fully evaporate any solvent residues. Finally, and imaging chamber is adhered to the substrate and polymers are rehydrated with solution of choice and placed into a Petri dish at 40 &#176;C for least 25 min to allow for the formation of polymersomes. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/54051/54051fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" src="/files/ftp_upload/54051/54051fig4.jpg" /> 
Figure 4. Polymersomes can form in a variety of different buffers. PEO-PBD polymer films were rehydrated with the indicated buffer at 40 &#176;C for 1 hr. Scale bar = 10 &#181;m. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/54051/54051fig4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" src="/files/ftp_upload/54051/54051fig5.jpg" /> 
Figure 5. Increasing the temperature during rehydration increases the size of the polymersomes. Representative epifluorescence images of polymersomes formed in water at the indicated rehydration temperatures. Increasing temperature results in larger polymersomes. Scale bar = 10 &#181;m. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/54051/54051fig5large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Temperature (&#176;C)</td>
			<td>Average Size (&#181;m)</td>
		</tr>
		<tr>
			<td>24</td>
			<td>2.93 &#177; 0.7</td>
		</tr>
		<tr>
			<td>40</td>
			<td>5.76 &#177; 2.5</td>
		</tr>
		<tr>
			<td>50</td>
			<td>6.65 &#177; 2.4</td>
		</tr>
		<tr>
			<td>60</td>
			<td>11.46 &#177; 5.8</td>
		</tr>
		<tr>
			<td>70</td>
			<td>14.04 &#177; 7.0</td>
		</tr>
	</tbody>
</table>
Table 1. Increasing the temperature during rehydration results in increased polymersome size. Average diameters for greater than 100 polymersomes in water per different temperature condition were calculated and are depicted here. Error is standard deviation.

Watch this Scientific Journal Video about Forming Giant-sized Polymersomes Using Gel-assisted Rehydration at JoVE.com

Forming Giant-sized Polymersomes Using Gel-assisted Rehydration

We present a protocol to rapidly form giant polymer vesicles (pGVs). Briefly, polymer solutions are dehydrated on dried agarose films adhered to coverslips. Rehydration of the polymer films results in rapid formation of pGVs. This method greatly advances the preparation of synthetic giant vesicles for direct applications in biomimetic studies.

Polymer vesicles, or polymersomes, are being widely explored as synthetic analogs of lipid vesicles based on their stability, robustness, barrier ...

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Universidad de Cartagena UDEC

Research

JoVE Journal

Bioengineering

9.3K Views.  Sandia National Laboratories. We present a protocol to rapidly form giant polymer vesicles (pGVs). Briefly, polymer solutions are dehydrated on dried agarose films adhered to coverslips. Rehydration of the polymer films results in rapid formation of pGVs. This method greatly advances the preparation of synthetic giant vesicles for direct applications in biomimetic studies.

Video: Forming Giant-sized Polymersomes Using Gel-assisted Rehydration

Preparation of Giant Vesicles Encapsulating Microspheres by Centrifugation of a Water-in-oil Emulsion

The constructive biology and the synthetic biology approach to creating artificial life involve the bottom-up assembly of biological or nonbiological materials. Such approaches have received considerable attention in research on the boundary between living and nonliving matter and have been used to construct artificial cells over the past two decades. In particular, Giant Vesicles (GVs) have often been used as artificial cell membranes. In this paper, we describe the preparation of GVs encapsulating highly packed microspheres as a model of cells containing highly condensed biomolecules. The GVs were prepared by means of a simple water-in-oil emulsion centrifugation method. Specifically, a homogenizer was used to emulsify an aqueous solution containing the materials to be encapsulated and an oil containing dissolved phospholipids, and the resulting emulsion was layered carefully on the surface of another aqueous solution. The layered system was then centrifuged to generate the GVs. This powerful method was used to encapsulate materials ranging from small molecules to microspheres.

Giant vesicles containing highly packed micrometer-sized components are useful cell models. The water-in-oil emulsion centrifugation method is a simple, powerful tool for the preparation of giant vesicles with encapsulated materials.

The constructive biology and the synthetic biology approach to creating artificial life involve the bottom-up assembly of biological or nonbiological ...

Biochemistry

Easy Manipulation of Architectures in Protein-based Hydrogels for Cell Culture Applications

Hydrogels are recognized as promising materials for cell culture applications due to their ability to provide highly hydrated cell environments. The field of 3D templates is rising due to the potential resemblance of those materials to the natural extracellular matrix. Protein-based hydrogels are particularly promising because they can easily be functionalized and can achieve defined structures with adjustable physicochemical properties. However, the production of macroporous 3D templates for cell culture applications using natural materials is often limited by their weaker mechanical properties compared to those of synthetic materials. Here, different methods were evaluated to produce macroporous bovine serum albumin (BSA)-based hydrogel systems, with adjustable pore sizes in the range of 10 to 70 &#181;m in radius. Furthermore, a method to generate channels in this protein-based material that are several hundred microns long was established. The different methods to produce pores, as well as the influence of pore size on material properties such as swelling ratio, pH, temperature stability, and enzymatic degradation behavior, were analyzed. Pore sizes were investigated in the native, swollen state of the hydrogels using confocal laser scanning microscopy. The feasibility for cell culture applications was evaluated using a cell-adhesive RGD peptide modification of the protein system and two model cell lines: human breast cancer cells (A549) and adenocarcinomic human alveolar basal epithelial cells (MCF7).

Different methods to manipulate three-dimensional architecture in protein-based hydrogels are evaluated here with respect to material properties. The macroporous networks are functionalized with a cell-adhesive peptide, and their feasibility in cell culture is evaluated using two different model cell lines.

Hydrogels are recognized as promising materials for cell culture applications due to their ability to provide highly hydrated cell environments. The field ...

Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst

Presented herein is a protocol for the facile synthesis of worm-like micelles by visible light mediated dispersion polymerization. This approach begins with the synthesis of a hydrophilic poly(oligo(ethylene glycol) methyl ether methacrylate) (POEGMA) homopolymer using reversible addition-fragmentation chain-transfer (RAFT) polymerization. Under mild visible light irradiation (&#955; = 460 nm, 0.7 mW/cm2), this macro-chain transfer agent (macro-CTA) in the presence of a ruthenium based photoredox catalyst, Ru(bpy)3Cl2 can be chain extended with a second monomer to form a well-defined block copolymer in a process known as Photoinduced Electron Transfer RAFT (PET-RAFT). When PET-RAFT is used to chain extend POEGMA with benzyl methacrylate (BzMA) in ethanol (EtOH), polymeric nanoparticles with different morphologies are formed in situ according to a polymerization-induced self-assembly (PISA) mechanism. Self-assembly into nanoparticles presenting POEGMA chains at the corona and poly(benzyl methacrylate) (PBzMA) chains in the core occurs in situ due to the growing insolubility of the PBzMA block in ethanol. Interestingly, the formation of highly pure worm-like micelles can be readily monitored by observing the onset of a highly viscous gel in situ due to nanoparticle entanglements occurring during the polymerization. This process thereby allows for a more reproducible synthesis of worm-like micelles simply by monitoring the solution viscosity during the course of the polymerization. In addition, the light stimulus can be intermittently applied in an ON/OFF manner demonstrating temporal control over the nanoparticle morphology.

This article describes a process for producing polymeric self-assembled nanoparticles using visible light mediated dispersion polymerization. Using low energy visible light to control the polymerization allows for the reproducible formation of self-assembled worm-like micelles at high solids content.

Presented herein is a protocol for the facile synthesis of worm-like micelles by visible light mediated dispersion polymerization. This approach begins ...

Chemistry

Directed Assembly of Elastin-like Proteins into defined Supramolecular Structures and Cargo Encapsulation In Vitro

Tailored proteinaceous building blocks are versatile candidates for the assembly of supramolecular structures such as minimal cells, drug delivery vehicles and enzyme scaffolds. Due to their biocompatibility and tunability on the genetic level, Elastin-like proteins (ELP) are ideal building blocks for biotechnological and biomedical applications. Nevertheless, the assembly of protein based supramolecular structures with distinct physiochemical properties and good encapsulation potential remains challenging.
Here we provide two efficient protocols for guided self-assembly of amphiphilic ELPs into supramolecular protein architectures such as spherical coacervates, fibers and stable vesicles. The presented assembly protocols generate Protein Membrane-Based Compartments (PMBCs) based on ELPs with adaptable physicochemical properties. PMBCs demonstrate phase separation behavior and reveal method dependent membrane fusion and are able to encapsulate chemically diverse fluorescent cargo molecules. The resulting PMBCs have a high application potential as a drug formulation and delivery platform, artificial cell, and compartmentalized reaction space.

At the interface of organic and aqueous solvents, tailored amphiphilic elastin-like proteins assemble into complex supramolecular structures such as vesicles, fibers and coacervates triggered by environmental parameters. The described assembly protocols yield Protein Membrane-Based Compartments (PMBCs) with tunable properties, enabling the encapsulation of various cargo.

Tailored proteinaceous building blocks are versatile candidates for the assembly of supramolecular structures such as minimal cells, drug delivery ...

Fabricating Degradable Thermoresponsive Hydrogels on Multiple Length Scales via Reactive Extrusion, Microfluidics, Self-assembly, and Electrospinning

While various smart materials have been explored for a variety of biomedical applications (e.g., drug delivery, tissue engineering, bioimaging, etc.), their ultimate clinical use has been hampered by the lack of biologically-relevant degradation observed for most smart materials. This is particularly true for temperature-responsive hydrogels, which are almost uniformly based on polymers that are functionally non-degradable (e.g., poly(N-isopropylacrylamide) (PNIPAM) or poly(oligoethylene glycol methacrylate) (POEGMA)). As such, to effectively translate the potential of thermoresponsive hydrogels to the challenges of remote-controlled or metabolism-regulated drug delivery, cell scaffolds with tunable cell-material interactions, theranostic materials with the potential for both imaging and drug delivery, and other such applications, a method is required to render the hydrogels (if not fully degradable) at least capable of renal clearance following the required lifetime of the material. To that end, this protocol describes the preparation of hydrolytically-degradable hydrazone-crosslinked hydrogels on multiple length scales based on the reaction between hydrazide and aldehyde-functionalized PNIPAM or POEGMA oligomers with molecular weights below the renal filtration limit. Specifically, methods to fabricate degradable thermoresponsive bulk hydrogels (using a double barrel syringe technique), hydrogel particles (on both the microscale through the use of a microfluidics platform facilitating simultaneous mixing and emulsification of the precursor polymers and the nanoscale through the use of a thermally-driven self-assembly and cross-linking method), and hydrogel nanofibers (using a reactive electrospinning strategy) are described. In each case, hydrogels with temperature-responsive properties similar to those achieved via conventional free radical cross-linking processes can be achieved, but the hydrazone cross-linked network can be degraded over time to re-form the oligomeric precursor polymers and enable clearance. As such, we anticipate these methods (which may be generically applied to any synthetic water-soluble polymer, not just smart materials) will enable easier translation of synthetic smart materials to clinical applications.

Protocols are described for the fabrication of degradable thermoresponsive hydrogels based on hydrazone cross-linking of polymeric oligomers on the bulk scale, microscale, and nanoscale, the latter for preparation of both gel nanoparticles and nanofibers.

While various smart materials have been explored for a variety of biomedical applications (e.g., drug delivery, tissue engineering, bioimaging, etc.), ...

Rapid, Scalable Assembly and Loading of Bioactive Proteins and Immunostimulants into Diverse Synthetic Nanocarriers Via Flash Nanoprecipitation

Nanomaterials present a wide range of options to customize the controlled delivery of single and combined molecular payloads for therapeutic and imaging applications. This increased specificity can have significant clinical implications, including decreased side effects and lower dosages with higher potency. Furthermore, the in situ targeting and controlled modulation of specific cell subsets can enhance in vitro and in vivo investigations of basic biological phenomena and probe cell function. Unfortunately, the required expertise in nanoscale science, chemistry and engineering often prohibit laboratories without experience in these fields from fabricating and customizing nanomaterials as tools for their investigations or vehicles for their therapeutic strategies. Here, we provide protocols for the synthesis and scalable assembly of a versatile non-toxic block copolymer system amenable to the facile formation and loading of nanoscale vehicles for biomedical applications. Flash nanoprecipitation is presented as a methodology for rapid fabrication of diverse nanocarriers from poly(ethylene glycol)-bl-poly(propylene sulfide) copolymers. These protocols will allow laboratories with a wide range of expertise and resources to easily and reproducibly fabricate advanced nanocarrier delivery systems for their applications. The design and construction of an automated instrument that employs a high-speed syringe pump to facilitate the flash nanoprecipitation process and to allow enhanced control over the homogeneity, size, morphology and loading of polymersome nanocarriers is described.

Nanomaterials provide versatile mechanisms of controlled therapeutic delivery for both basic science and translational applications, but their fabrication often requires expertise that is unavailable in most biomedical laboratories. Here, we present protocols for the scalable fabrication and therapeutic loading of diverse self-assembled nanocarriers using flash nanoprecipitation.

Nanomaterials present a wide range of options to customize the controlled delivery of single and combined molecular payloads for therapeutic and imaging ...

Lipid Vesicle Encapsulation Protocol for Complex Protein Networks

Construction of Out&#45;of&#45;Equilibrium Metabolic Networks in Nano&#45; and Micrometer&#45;Sized Vesicles

We present a method to incorporate into vesicles complex protein networks, involving integral membrane proteins, enzymes, and fluorescence-based sensors, using purified components. This method is relevant for the design and construction of bioreactors and the study of complex out-of-equilibrium metabolic reaction networks. We start by reconstituting (multiple) membrane proteins into large unilamellar vesicles (LUVs) according to a previously developed protocol. We then encapsulate a mixture of purified enzymes, metabolites, and fluorescence-based sensors (fluorescent proteins or dyes) via freeze-thaw-extrusion and remove non-incorporated components by centrifugation and/or size-exclusion chromatography. The performance of the metabolic networks is measured in real time by monitoring the ATP/ADP ratio, metabolite concentration, internal pH, or other parameters by fluorescence readout. Our membrane protein-containing vesicles of 100-400 nm diameter can be converted into giant-unilamellar vesicles (GUVs), using existing but optimized procedures. The approach enables the inclusion of soluble components (enzymes, metabolites, sensors) into micrometer-size vesicles, thus upscaling the volume of the bioreactors by orders of magnitude. The metabolic network containing GUVs are&#160;trapped in microfluidic devices for analysis by optical microscopy.

Author Spotlight: Tackling Challenges in Synthetic Cell Engineering

We present a protocol for reconstituting membrane proteins and encapsulating enzymes and other water-soluble components in lipid vesicles of sub-micrometer and micrometer size.

We present a method to incorporate into vesicles complex protein networks, involving integral membrane proteins, enzymes, and fluorescence-based sensors, ...

Modulating Shape of Polyester Based Polymersomes using Osmotic Pressure

Polymersomes are membrane-bound, bilayer vesicles created from amphiphilic block copolymers that can encapsulate both hydrophobic and hydrophilic payloads for drug delivery applications. Despite their promise, polymersomes are limited in application due to their spherical shape, which is not readily taken up by cells, as demonstrated by solid nanoparticle scientists. This article describes a salt-based method for increasing the aspect ratios of spherical poly(ethylene glycol) (PEG)- based polymersomes. This method can elongate polymersomes and ultimately control their final shape by adding sodium chloride in post-formation dialysis. Salt concentration can be varied, as described in this method, based on the hydrophobicity of the block copolymer being used as the base for the polymersome and the target shape. Elongated nanoparticles have the potential to better target the endothelium in larger diameter blood vessels, like veins, where margination is observed. This protocol can expand therapeutic nanoparticle applications by utilizing elongation techniques in tandem with the dual-loading, long-circulating benefits of polymersomes.

Polymersomes are self-assembled polymeric vesicles that are formed in spherical shapes to minimize Gibb's Free Energy. In the case of drug delivery, more elongated structures are beneficial. This protocol establishes methods to create more rod-like polymersomes, with elongated aspect ratios, using salt to induce osmotic pressure and reduce internal vesicle volumes.

Polymersomes are membrane-bound, bilayer vesicles created from amphiphilic block copolymers that can encapsulate both hydrophobic and hydrophilic payloads ...

Rapid Encapsulation of Reconstituted Cytoskeleton Inside Giant Unilamellar Vesicles

Giant unilamellar vesicles (GUVs) are frequently used as models of biological membranes and thus are a great tool to study membrane-related cellular processes in vitro. In recent years, encapsulation within GUVs has proven to be a helpful approach for reconstitution experiments in cell biology and related fields. It better mimics confinement conditions inside living cells, as opposed to conventional biochemical reconstitution. Methods for encapsulation inside GUVs are often not easy to implement, and success rates can differ significantly from lab to lab. One technique that has proven to be successful for encapsulating more complex protein systems is called continuous droplet interface crossing encapsulation (cDICE). Here, a cDICE-based method is presented for rapidly encapsulating cytoskeletal proteins in GUVs with high encapsulation efficiency. In this method, first, lipid-monolayer droplets are generated by emulsifying a protein solution of interest in a lipid/oil mixture. After being added into a rotating 3D-printed chamber, these lipid-monolayered droplets then pass through a second lipid monolayer at a water/oil interface inside the chamber to form GUVs that contain the protein system. This method simplifies the overall procedure of encapsulation within GUVs and speeds up the process, and thus allows us to confine and observe the dynamic evolution of network assembly inside lipid bilayer vesicles. This platform is handy for studying the mechanics of cytoskeleton-membrane interactions in confinement.

This article introduces a simple method for expeditious production of giant unilamellar vesicles with encapsulated cytoskeletal proteins. The method proves to be useful for bottom-up reconstitution of cytoskeletal structures in confinement and cytoskeleton-membrane interactions.

Giant unilamellar vesicles (GUVs) are frequently used as models of biological membranes and thus are a great tool to study membrane-related cellular ...

Giant Liposome Preparation for Imaging and Patch-Clamp Electrophysiology

The reconstitution of ion channels into chemically defined lipid membranes for electrophysiological recording has been a powerful technique to identify and explore the function of these important proteins. However, classical preparations, such as planar bilayers, limit the manipulations and experiments that can be performed on the reconstituted channel and its membrane environment. The more cell-like structure of giant liposomes permits traditional patch-clamp experiments without sacrificing control of the lipid environment.
Electroformation is an efficient mean to produce giant liposomes &gt;10 &mu;m in diameter which relies on the application of alternating voltage to a thin, ordered lipid film deposited on an electrode surface. However, since the classical protocol calls for the lipids to be deposited from organic solvents, it is not compatible with less robust membrane proteins like ion channels and must be modified. Recently, protocols have been developed to electroform giant liposomes from partially dehydrated small liposomes, which we have adapted to protein-containing liposomes in our laboratory.
We present here the background, equipment, techniques, and pitfalls of electroformation of giant liposomes from small liposome dispersions. We begin with the classic protocol, which should be mastered first before attempting the more challenging protocols that follow. We demonstrate the process of controlled partial dehydration of small liposomes using vapor equilibrium with saturated salt solutions. Finally, we demonstrate the process of electroformation itself. We will describe simple, inexpensive equipment that can be made in-house to produce high-quality liposomes, and describe visual inspection of the preparation at each stage to ensure the best results.

Reconstituting functional membrane proteins into giant liposomes of defined composition is a powerful approach when combined with patch-clamp electrophysiology. However, conventional giant liposome production may be incompatible with protein stability. We describe protocols for producing giant liposomes from pure lipids or small liposomes containing ion channels.

The reconstitution of ion channels into chemically defined lipid membranes for electrophysiological recording has been a powerful technique to identify ...