Pulling Membrane Nanotubes from Giant Unilamellar Vesicles

Summary

Many proteins in the cell sense and induce membrane curvature. We describe a method to pull membrane nanotubes from lipid vesicles to study the interaction of proteins or any curvature-active molecule with curved membranes in vitro.

Abstract

The reshaping of the cell membrane is an integral part of many cellular phenomena, such as endocytosis, trafficking, the formation of filopodia, etc. Many different proteins associate with curved membranes because of their ability to sense or induce membrane curvature. Typically, these processes involve a multitude of proteins making them too complex to study quantitatively in the cell. We describe a protocol to reconstitute a curved membrane in vitro, mimicking a curved cellular structure, such as the endocytic neck. A giant unilamellar vesicle (GUV) is used as a model of a cell membrane, whose internal pressure and surface tension are controlled with micropipette aspiration. Applying a point pulling force on the GUV using optical tweezers creates a nanotube of high curvature connected to a flat membrane. This method has traditionally been used to measure the fundamental mechanical properties of lipid membranes, such as bending rigidity. In recent years, it has been expanded to study how proteins interact with membrane curvature and the way they affect the shape and the mechanics of membranes. A system combining micromanipulation, microinjection, optical tweezers, and confocal microscopy allows measurement of membrane curvature, membrane tension, and the surface density of proteins, concurrently. From these measurements, many important mechanical and morphological properties of the protein-membrane system can be inferred. In addition, we lay out a protocol of creating GUVs in the presence of physiological salt concentration, and a method of quantifying the surface density of proteins on the membrane from fluorescence intensities of labeled proteins and lipids.

Introduction

Many cellular processes, such as endocytosis, trafficking, the formation of filopodia, infection, etc., are accompanied by a dramatic change in the shape of cell membranes^1,2. In the cell, a number of proteins participate in these processes by binding to the membrane and altering their shape. The most notable examples are members of the Bin/Amphiphysin/Rvs (BAR) protein family, containing a characteristic intrinsically curved BAR domain^3,4,5,6,7. Typically, they interact with the membrane by adhering the BAR domain to the surface and, in many cases, also shallowly inserting amphipathic helices into the bilayer. The shape, size, and charge of the BAR domain together with the number of amphipathic helices determines: (1) the direction of membrane curvature (i.e., whether they will induce invaginations or protrusions), and (2) the magnitude of membrane curvature^5,8. Of note, here positive curvature is defined as the convex side of the curved membrane, i.e., the bulge toward the interacting particle, and negative otherwise. Moreover, quantitative studies of BAR proteins revealed that their effect on the membrane depends on a set of physical parameters: surface density of proteins, membrane tension, and membrane shape (flat versus tubular versus spherical shape)⁷. Depending on these parameters BAR proteins can: (1) act as sensors of membrane curvature, (2) bend membranes, or (3) induce membrane scission⁷.

Due to the sheer number of components involved in membrane reshaping in the cell, studying the quantitative aspects of the phenomena, such as endocytosis, in vivo is extremely challenging. In vitro reconstitution of minimal components mimicking curved membranes in the cell provides means to gain a mechanistic understanding of how membrane-curving proteins operate. This article describes a protocol to reconstitute a membrane nanotube in vitro using micromanipulation, confocal microscopy, and optical tweezers. The approach can be used to study, in a quantitative way, how proteins, lipids, or small molecules interact with curved membranes. Lipid GUVs are used as models of a cell membrane, whose curvature is negligible compared to the size of interacting membrane-curving molecules. They are prepared using the electroformation method⁹ in which the vesicles are formed by hydrating a lipid film and swelling it into GUVs under an alternating current (AC)¹⁰. Most common substrates on which GUVs are grown are either semi-conductive plates coated with indium tin oxide (ITO) or platinum wires (Pt-wires)¹¹. In this work, GUVs are grown on Pt-wires as this method has been shown to work much better than the alternative in making GUVs in the presence of salts in the buffer¹². Although the electroformation protocol is described here in sufficient detail to reproduce it, we refer the reader to previous articles in which similar and other methods of making GUVs have been described in detail^13,14. In our hands, electroformation on Pt-wires has successfully yielded GUVs from a mix of synthetic lipids or from natural lipid extracts in a buffer containing ~100 mM NaCl. Furthermore, it was also possible to encapsulate proteins inside GUVs during growth. An example electroformation chamber is shown in Figure 1A; it comprises two ~10-cm-long Pt-wires inserted into a holder made from polytetrafluoroethylene (PTFE) that can be sealed on both sides with glass coverslips ~1 - 2 cm apart (Figure 1A).

Figure 1: Experimental setup. (A) The GUV electroformation chamber with electrical connectors attached to Pt-wires. (B) Left: the experimental system showing the microscope, the experimental chamber above the objective and two micropipettes (left and right) attached to the micromanipulators and inserted into the experimental chamber for tube pulling and protein injection. Right: a close-up view of the experimental chamber mounted above the objective showing the tips of the aspiration and the injection micropipettes inserted. (C) A syringe equipped with a thin dispenser inserted into a micropipette at its back end. The bottom is a close-up view of the dispenser inside the micropipette with the blue dotted line outlining the micropipette. This system is used to fill the micropipette with casein to passivate the glass surface and also to back fill with mineral oil when needed. (D) A system used to aspirate µL quantities of the protein solution. The needle is connected to a syringe and to tubing which is connected to the injection micropipette. The micropipette tip is carefully immersed into the protein solution and aspirated so to fill the micropipette tip. The micropipette is then back filled with mineral oil using the system shown in panel C. Please click here to view a larger version of this figure.

A membrane nanotube, ranging in radius from 7 nm to several hundred nm, can be pulled from a GUV by an external force. This method was initially designed to measure the elastic properties of cell membranes and vesicles, such as the bending rigidity^15,16. In most recent works, the method was extended to study the interaction of proteins with curved membranes by microinjecting the proteins near the pulled nanotube^7,17. Other methods have been developed for studying membrane-curving proteins. In one method, proteins are incubated with differently sized liposomes tethered to a passivated surface. Confocal microscopy is used to measure the protein binding as a function of liposome diameter, which can indicate curvature-induced sorting^18,19. In another method, proteins are injected near a micro-aspirated GUV to measure their ability to spontaneously induce tubules^20,21. The method described in this protocol is uniquely suited to study membrane-curving proteins involved in endocytosis, where most proteins typically encounter preformed membrane nanotubes connecting the cargo-containing membrane invagination with the underlying flat plasma membrane. Furthermore, in this method, unlike in the assay with tethered small liposomes, the membrane nanotube is continuously connected to the membrane; therefore, it is in mechanical equilibrium with the GUV, a situation expected in vivo. Hence, fundamental membrane physics applies and we can infer a plethora of mechanical properties from our measurements^22,23,24.

For a full implementation of this method, the necessary equipment includes a confocal microscope, optical tweezers, and one or two micropipettes connected to a water tank (Figure 1B). By combining all three, it is possible to simultaneously measure membrane tension, membrane curvature, surface density of proteins, and tube force²⁵. Micropipette aspiration is essential and it is easily constructed by inserting a glass micropipette into a holder connected to a water tank, which, via hydrostatic pressure, controls the aspiration pressure²⁶. The micropipette and the holder are controlled by a micromanipulator and, ideally, in one direction by a piezo-actuator for precision movement. To pull a nanotube, the microaspirated GUV is briefly stuck to a micron-sized bead then pulled away creating a nanotube. In this implementation, the bead is held by optical tweezers, which can be constructed by following a published protocol²⁷. It is possible to dispense of the optical tweezers and pull nanotubes in different ways, although at the cost of accurate force measurements. If it is too challenging to build an optical trap or if force measurements are not essential, such as if one simply wants to check the preference of proteins for curved membranes, a tube can be pulled using a bead aspirated at the tip of a second micropipette²⁸. It is also possible to pull tubes using gravitational force²⁹ or flow^30,31. Furthermore, confocal microscopy is not essential either; however, it is preferred so to measure the surface density of proteins. It also allows measuring the nanotube radius from fluorescence intensity of lipids in the tube, thus independently of membrane force and tension. Inferring tube radius from fluorescence is particularly important if the relationship between these quantities deviates from well-established equations due to the presence of membrane-adhered proteins²⁵. Importantly, one cannot dispense of both the optical trap and confocal microscopy, as it will not be possible to measure the tube curvature.

The method as described in this protocol has been used to study the curvature-induced sorting of various peripheral membrane proteins on nanotubes, mostly those from the BAR family^25,32,33,34. It was also shown that the conically shaped transmembrane potassium channel KvAP is enriched on curved nanotubes in the same way as BAR proteins³⁵. By optimizing the method to encapsulate proteins inside GUVs, the interaction of proteins with negative curvature has been recently investigated as well³⁶. Furthermore, this method has been used to elucidate the formation of protein scaffolds^25,37 and to study the mechanism of membrane scission by either line tension³⁸, protein dynamin³⁹, or by BAR proteins^40,41. In addition to proteins, small molecules or ions can also induce curvature. Using this method, calcium ions were shown to induce positive curvature under salt-free conditions⁴². Interestingly, it has also been shown that lipids can undergo curvature sorting, although only for compositions that are near a demixing point^43,44. In sum, the method can be used by researchers interested in investigating how either integral membrane components (e.g., lipids or transmembrane proteins) or peripherally binding molecules (either inside or outside GUVs) interact with cylindrically curved membranes, from mechanical and quantitative points of view. It is also intended for those interested in measuring the mechanical properties of the membrane itself^22,23,45.

Protocol

1. Preparation of GUVs by Electroformation on Pt-wires

1. Clean the electroformation chamber (see Introduction and Figure 1A) and the Pt-wires with an organic solvent such as ethanol or acetone to wash away the lipids and with water to wash away the salts.
   NOTE: We suggest thoroughly wiping away the residue with ethanol-soaked tissue then sonicating in acetone, ethanol, then water, each for 5 min.
2. Prepare a lipid mix of a desired lipid composition at 1 mg/mL in chloroform. The mix should contain ~ 0.05% molar fraction of a lipid conjugated with biotin (e.g., 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[biotinyl(polyethyleneglycol)-2000]) and ~ 0.5% molar fraction of a lipid conjugated with a fluorophore (e.g., BODIPY-TR-C5-ceramide).
   NOTE: In our experience, it was difficult to produce GUVs at a high yield containing more than 30% charged lipids.
   CAUTION: Chloroform should be handled inside a chemical hood wearing appropriate gloves.
3. Insert a pair of Pt-wires into the electroformation chamber. Deposit the lipid mix onto the Pt-wires in drops separated by ~ 2-3 mm (total ~ 4 µL of the mix).
4. Dry the wires under vacuum for 30–60 min at room temperature.
5. Seal the bottom of the chamber by adhering the coverslip over the chamber using silicon grease. Fill the chamber with a buffered solution containing NaCl, sucrose, and a buffering agent (e.g., 70 mM NaCl, 100 mM sucrose, and 10 mM Tris, at pH 7.4). This medium will be inside the GUVs in the experiment. It is essential that the osmolarity of this medium match the osmolarity of the experimental medium within ~ 10%. Use sucrose to adjust the osmolarity. Add proteins to the solution at a desired concentration if the goal is to encapsulate them in the GUVs.
   CAUTION: Various salts and sugars in the buffer can affect the bending rigidity and the spontaneous curvature of membranes^24,42,46,47.
6. Seal the top of the chamber by adhering a coverslip with silicon grease ensuring minimum air inside the chamber. Apply a sine AC current through the Pt-wires at 500 Hz and 280 mV.
   NOTE: The growth time and temperature must be optimized depending on the lipid composition and the sensitivity of the protein. When using natural lipid extracts, and also when encapsulating proteins in GUVs, the best yield was achieved by growing GUVs at 4 °C overnight. In the absence of proteins, and for synthetic lipid compositions, growth at room temperature for ~ 2 h was sufficient.

2. Preparation of the Experimental Chamber and the Micropipettes

1. To prepare micropipettes, pull a glass capillary using a pipette puller. It is suggested to use a glass capillary with internal and external radii of, respectively, 0.7 mm and 1 mm. Then, refine the tip of the micropipette so that its inner diameter is 5–7 µm, by using a microforge. If proteins or other molecules will be injected in the experiment, pull another micropipette and refine its tip to a inner diameter of 8–15 µm.
2. Construct an experimental chamber by placing two rectangular microscopy coverslips onto a metallic base as shown in Figure 1. The coverslips should be separated by ~ 1 mm. The chamber should have openings along the long edges (see Figure 1). The open sides should fit the tip of the micropipette where the tip should reach at least the center of the chamber.
3. Prepare the experimental buffer whose osmolarity should not differ by more than 10% from the buffer used to grow GUVs. Adjust the osmolarity with glucose. An example of an experimental buffer that was used in studying the interaction of endophilin with nanotubes is 100 mM NaCl, 40 mM glucose, buffered with Tris to pH 7.4. A combination of sucrose inside/glucose outside ensures: (a) sufficient phase contrast to observe GUVs with bright field microscopy, and (b) higher density inside the GUVs which causes them to settle on the bottom of the chamber. Adjust salt concentration based on experimental requirement.
   NOTE: In addition to affecting the membrane's mechanical properties, in our experience, high glucose concentration (> 300 mM) negatively affects the establishment of streptavidin-biotin bonds, required to pull a nanotube. Furthermore, too little salt inhibits streptavidin-biotin bonds, while too high of a concentration screens protein-membrane interactions. In case of protein encapsulation, using very high salt concentration in the external buffer (e.g., >200 mM NaCl) can be used as a trick to detach the proteins from the outer leaflet³⁶. It is necessary to experiment with a range of salt concentration to find the optimal binding conditions of the molecule of interest.
4. 30–60 min before collecting GUVs for the experiment, passivate the glass surfaces by filling both the experimental chamber and the aspiration micropipette with a 5 mg/mL solution of a highly pure β-casein (e.g., dissolved in the experimental buffer). β-casein creates a protective layer on the glass surfaces, preventing GUVs to adhere too strongly, which would cause them to burst. Incubate with β-casein for 30–60 min.
   NOTE: There should be no bubbles inside the micropipette that would interfere with controlling membrane tension.
   1. To build a dispenser for filling micropipettes, break a syringe needle close to the plastic connector and glue into it a thin silica capillary (such as those used for liquid chromatography) (Figure 1C).
5. During incubation with β-casein, mount the chamber on the microscope and center it above the objective. Insert the tip of the aspiration micropipette through the opening along the long edge and bring the tip above the microscope objective. Adjust the water tank level so that the aspiration pressure is near zero (there should be no heavy flow in or out of the pipette, which can be seen under the microscope).
6. In case the proteins or other molecules will be injected during the experiment, fill the injection micropipette with the desired molecule dissolved in the experimental buffer at a concentration of choice, mount the micropipette inside a micromanipulator, and insert through the opposite side of the experimental chamber.
   1. To use a minimum amount of proteins, fill only the micropipette tip with the protein by aspiration. To do that, wrap the end of a needle attached to a syringe with plastic tubing. Insert the tubing into the back of the injection micropipette.
   2. Very carefully immerse the tip of the micropipette into the protein solution and aspirate it to fill the tip of the micropipette.
      NOTE: This simple setup is shown in Figure 1D and, in our experience, it allows aspirating from as little as a few µL of the protein solution.
   3. Backfill the rest of the injection micropipette with mineral oil to prevent mixing of the protein solution and the water from the water tank (using the setup in Figure 1C).
   4. Take care not to introduce air bubbles into the injection pipette, as it will induce unstable injection pressure. Alternatively, if the protein quantity is sufficient, fill the micropipette with the proteins the same way as filling with β-casein as described in step 2.4. Adjust the water tank level to minimize the aspiration pressure in the injection pipette.
      NOTE: The concentration of the injected molecule or ion near the nanotube is going to be lower due to dilution and it can be estimated by measuring the fluorescence intensity decrease as a function of the distance from the pipette exit⁴². It is however more important to know the bilayer-bound density of the injected molecule, which can be precisely measured (see Section 4).
7. After incubation with β-casein, remove the solution from the chamber, and rinse with the experimental buffer several times. Fill with the experimental buffer.
8. Stop electroformation of GUVs and collect them directly from the Pt-wires. Add a few µL of the GUV solution to the experimental chamber. Use only freshly prepared GUVs.
9. Add a few µL of streptavidin-coated beads to the experimental chamber to a final concentration of beads in the chamber at around 0.1 x 10⁻³ % (w/v) or less. Polystyrene beads ~3 µm in diameter are recommended (polystyrene beads in water have a near-optimal refractive index contrast with regards to maximizing the gradient force with respect to the scattering force in the optical trap). The bead concentration can be adjusted based on the experiment: a very low concentration makes it difficult to find them in the chamber, and a too high concentration runs the risk of multiple beads falling into the optical tweezers.

3. Pulling a Membrane Nanotube from a GUV

1. Let the GUVs and the beads settle to the bottom of the chamber. Deflate the GUVs by letting a little of the experimental buffer evaporate, for approximately ~ 15 min. Deflating the GUVs is essential to produce some excess area that can be aspirated with the micropipette. GUVs should visibly undulate (i.e., appear floppy) under the light microscope. If they appear tense, allow for more evaporation time.
   NOTE: The osmolarity change rate depends on the evaporating surface area, the temperature, etc., and should be closely monitored. In principle, the osmolarity difference could be set from start by adjusting the sucrose/glucose concentration, however, care should be taken not to induce an osmotic shock.
2. Find a floppy GUV and aspirate it into the pipette. The length of the aspiration tongue (the part of the membrane inside the pipette) should be equal to or larger than the pipette radius for the theoretical analysis to be applicable^15,16,22,23 (Figure 2). Try several GUVs. If none of the GUVs can be aspirated to produce a long enough tongue, wait a few more minutes. If GUVs are floppy enough, proceed to the next step.
3. Seal the chamber with mineral oil, to prevent further evaporation of the buffer. Do so by carefully pipetting the oil along the open edges of the experimental chamber.
4. To set the zero position of the aspiration pressure, first, look for a bead in the chamber and position the aspiration pipette exit near the bead. Adjust the height of the water tank so that the bead is neither sucked in nor blown away by the aspiration pipette. Although the mineral oil prevents evaporation and therefore further pressure changes inside the chamber, zero the aspiration pressure before measuring each GUV.
5. Find a GUV and aspirate it. Move the micropipette up and out of focus (to keep the GUV away from the surface where it might be pulled out of the pipette by shear stress when the chamber is moved).
6. Look for a bead by carefully moving around the chamber. Sudden moves can eject the GUV. Trap it with optical tweezers at a distance ~ 20 µm away from the chamber bottom. Ensure that the region of interest is clean with no other beads or membranes in sight. Anything falling in the optical tweezers other than the bead will disrupt the measurement.
7. Bring the GUV back into focus, and away from the bead with the micropipette aligned with the optical trap (Figure 2).
8. Record the movement of the bead for 1–2 min to measure the equilibrium position (required for force measurements).
9. Reduce the pressure inside the micropipette as much as possible without losing the GUV so to decrease the membrane tension. Carefully bring the GUV in contact with the bead for around a second, establishing streptavidin-biotin bonds, then gently pull back creating a nanotube. The motion of the GUV toward or away from the bead should ideally be done with a piezo-actuator to minimally disrupt the bead in the optical tweezers.
   NOTE: If the nanotube does not form, it could be due to poor streptavidin coating of the bead, insufficient amount of biotinylated lipids in the GUV, insufficient concentration of salt or excessive concentration of glucose in the experimental buffer, or the membrane tension in the GUV is too high⁴⁸.
10. Increase the aspiration pressure so to recreate the aspiration tongue. Align the tube to lie in the axis of the aspiration pipette and maximally focus on the tube (Figure 2).
11. Ensure that the GUV equator and the tube are in focus. Record the movement of the bead with bright field microscopy for a few min (here, the camera acquisition speed is 30 Hz). Record the height, h, of the water tank with respect to the zero position. Take a few confocal images of the system (Figure 2).
12. Repeat the previous step at different aspiration pressures, implicitly membrane tensions.Typical tension range is 0.015–0.2 mN/m, with a step size of around 0.02 mN/m.
13. If injecting proteins or molecules near the system, bring the injection micropipette near the nanotube, making sure that the bead in the optical trap is not perturbed. Gently inject at a pressure of around 1–2 Pa.
14. After the protein binding has equilibrated (the fluorescence intensity of the injected protein on the membrane remains constant on the GUV), repeat the step-wise measurements as with the bare membrane (steps 3.11 and 3.12).
    NOTE: Since the measurements are performed while injecting proteins near the GUV at constant pressure, the bulk concentration of the protein remains roughly unchanged near the GUV; thus, protein desorption should be negligible during the measurement.
    1. Alternatively, it is possible to incubate the GUVs together with the proteins before performing tube-pulling experiments to ensure a constant protein bulk concentration. Given that the relative membrane fraction of proteins on the tube and on the GUV is measured, the way proteins are delivered does not influence the curvature-sorting calculation (see Section 4).

Figure 2: Tube-pulling experiment. (A) Schematics of the experiment. (B) A confocal image of a pulled tube as described in this Protocol. Scale bar = 2 µm. Please click here to view a larger version of this figure.

4. Measurements and Data Analysis

1. Measuring membrane tension
   1. Calculate the hydrostatic pressure for each step at constant aspiration pressure:
      ΔP = pgh
      where p is the water density, g gravitational acceleration, and h the height of the water tank from step 3.11.
   2. From confocal images, measure the radius of the GUV, r_GUV, and the radius of the aspiration pipette, r_pip (Figure 2).
   3. Calculate the membrane tension, σ, using Laplace's equation⁴⁹:
      
2. Measuring membrane force
   1. Determine the stiffness of the optical tweezers, k, by using one of several calibration methods²⁷. In this setup, measure k using the viscous drag method²⁷.
   2. Calculate the equilibrium position of the bead, a₀, as an average from a measurement before pulling the tube (step 3.8).
   3. For each constant tension measurement, calculate the equilibrium membrane force, F, from Hooke's law:
      F = k(a - a₀)
      where a is the average position of the bead during that measurement.
3. Measuring tube radius
   1. In the case of a bare membrane (no added membrane-curving molecules), calculate the tube radius, R, from the force as:
      R = F/(4πσ)
      (references^22,23).
   2. To measure the tube radius in the presence of membrane-curving molecules and independently of step 4.3.1, first, record the lipid fluorescence intensity along the tube length, I_tub, and along the GUV contour, I_GUV. Measure the average fluorescence intensity of a fluorophore in or bound to the membrane as an average intensity along the brightest line of a tube or a GUV contour. Select a rectangular box containing a horizontal section of the GUV contour or the tube and calculate the sum of the fluorescence intensities of each horizontal line in the box.
      1. Divide each sum by the number of pixels of the horizontal line (i.e., the box width). Note that in the selected box, there should be no other membranes present. The fluorescence intensity profile along the length of the selected box is obtained.
      2. After subtracting the background intensity, take the average pixel fluorescence intensity from the brightest line. The tube radius is linearly related to the ratio of fluorescence along the contour of the tube and of the GUV as:
         R = K_tubI_tub/I_GUV
         where K_tub is a calibration factor²⁵.
         NOTE: This method can be used to measure the tube radius in the 10–80 nm range (when the tube is narrow enough to lie within one confocal voxel width) and with a somewhat greater uncertainty in the 80 nm and higher range. The sensitivity of the measurement depends on the setup.
   3. Determine K_tub by performing independent radius measurements in steps 4.3.1 and 4.3.2 on a simple membrane composition using uncharged lipids. Such simple membrane composition ensures that the radius and the force have the simple relationship given in step 4.3.1. Repeat the experiment several times and plot R, deduced from the force (step 4.3.1) versus I_tub/I_GUV (step 4.3.2). Calculate K_tub from the fit. In this setup, K_tub = 200 ± 50 nm by using egg L-α-phosphatidylcholine (egg-PC) membrane and a fluorescent lipid whose fluorescence minimally depends on polarization²⁵.
      NOTE: K_tub must be measured for different objectives, due to their different confocal voxel volumes. The lipid fluorophore should not interact with the injected proteins/molecules. The fluorescent lipid recommended here, BODIPY TR ceramide, is not expected to have any interactions with the proteins. This assumption was confirmed with previous studies of BAR and I-BAR domains^25,36,37, which have shown that at high protein surface coverage, the tube radius is fixed by the proteins, regardless of the tension in the GUV. If proteins interact with the lipid fluorophore, a depletion or enrichment of the fluorophore will be observed in the tube at varied high protein surface fractions.
4. Measuring the surface density of proteins
   1. Prepare lipid mixes using a simple uncharged lipid (e.g., egg-PC) supplemented with about five different mole fractions of a fluorescent lipid (of the same wavelength as the dye used to label the protein, e.g., BODIPY-FLC5-hexadecanoyl-phosphatidylcholine (HPC*) for e.g., the Alexa488-labeled protein) in the range: X_HPC* = 0.01–1%. Prepare GUVs in 100 mM sucrose by electroformation on ITO plates (follow step 1 of a previous publication¹³).
   2. Collect GUVs and transfer to an experimental chamber passivated with β-casein. Use e.g., 100 mM glucose for the experimental solution. Wait a few minutes for the GUVs to settle.
   3. Take confocal fluorescence images of GUVs and record the average fluorescence intensity along the GUV contours as a function of the mole fraction of the fluorescent lipid (see Step 4.3.2). For each composition, calculate the area density of the fluorescent lipid, φ_HPC*. For example, by assuming that the area per lipid is 0.7 nm², φ_HPC* = 1.43 x 10⁶ X_HPC* per leaflet. Plot HPC* fluorescence intensity in the GUV, I_HPC*,GUV, versus φ_HPC*. Fit gives the calibration constant, A, given by φ_HPC* = AI_HPC*,GUV. A depends on the microscopy settings, such as the laser power and the detector sensitivity (i.e., gain), therefore record A for various commonly used microscopy settings (see example in Figure 3).
   4. Prepare several solutions of HPC* dissolved in detergent, e.g., sodium dodecyl-sulfate (SDS), at different concentrations in the range from ~ 1 to 10-50 µM. Record fluorescence intensity of each solution in bulk and calculate the slope of intensity versus concentration (Figure 3). Repeat the measurement with the fluorophore that will be conjugated to the protein in a similar concentration range (see the example with Alexa488 in Figure 3). This measurement is required to relate the fluorescence intensities of the protein label and the lipid label, I_A488,bulk / I_HPC*,bulk, as they may not necessarily emit in the same way at the same bulk concentration.
   5. Measure the number of fluorophores per protein molecule using a fluorospectrometer. For example, for the case of Alexa488, the number of Alexa488 molecules per protein, n_A488, can be calculated using the following relation:
      n_A488 = (A₄₉₄/ε_A488)/((A₂₈₀ - 0.11A₄₉₄) / ε_prot)
      where A₄₉₄ and A₂₈₀ are the absorbance values per unit length at 494 nm and 280 nm, respectively, and ε_A488 and ε_prot are the molecular absorption coefficients of Alexa488 and the protein, respectively.
   6. Calculate the surface density of the protein on the GUV, φ_prot,GUV, according to the following formula:
      
      Keep in mind the polymerization state of the protein. For example, BAR proteins dimerize, therefore the calculated density will be that of the BAR monomer per area if using the extinction coefficient of the monomeric form.

Figure 3: An example of protein surface density calibration. Measured are the HPC* lipid fluorescence intensity in bulk (left) and in GUVs (center). Also, measured are the bulk fluorescence intensity of Alexa488 (bound to a BAR domain) (right). Fluorescence intensity linearly scales with concentration. Measurements shown are for specific detection gain and laser power output. Plots generated based on data from reference³⁷. Please click here to view a larger version of this figure.

Results

The tube-pulling experiment can give vital mechanical information about the membrane. In the absence of proteins or other molecules that couple with membrane curvature, the membrane force and tube radius can be related with membrane tension by applying the Canham-Helfrich Hamiltonian equation to a tube pulled from a GUV^50,51

Discussion

The method of pulling tubes from GUVs gives rich information on the membrane-protein system, as it is not only the means to measure the fundamental mechanical properties of the membrane, but it helps to shed light on the coupling between proteins and membrane curvature. As discussed in the Introduction, other techniques exist to measure the effects of membrane-curving proteins, either by incubating the proteins with sub-micron liposomes tethered to a passivated surface^18,

Materials

Name	Company	Catalog Number	Comments
1,2-Dioleoyl-sn-glycero-3-phosphatidylcholine (DOPC)	Avanti	850375	Example lipid used in data for Figure 3
1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[biotinyl(polyethyleneglycol)-2000] [DSPE-PEG(2000)-biotin]	Avanti	880129	biotinylated lipid
BODIPY-TR-C5-ceramide	Molecular Probes (ThermoFisher)	D7540	fluorescent lipid
BODIPY- FLC5-hexadecanoyl phosphatidylcholine (HPC*)	Molecular Probes (ThermoFisher)		fluorescent lipid for protein density calibration
egg L-α-phosphatidylcholine (eggPC)	Avanti	840051	used for calibrating the tube radius constant
β-casein from bovine milk (>99%)	Sigma Aldrich	C6905	used for passivating the micropipette and the experimental chamber
Sucrose	Sigma Aldrich	S7903
D(+) glucose	Sigma Aldrich	G7021
NaCl	Sigma Aldrich	S7653
Tris	Sigma Aldrich	10708976001
osmometer	Loser	n/a
Pt-wires, 0.5 mm diameter, 99.99% pure	Goodfellow USA	PT005139	used for GUV electroformation
function generator		n/a	used to create current for GUV electroformation
putty sealant	Vitrex (from CML France)	CRIT 140013	used to seal the electroformation chamber
bath sonicator		n/a	useful to clean the electroformation chamber, but not crucial
Nikon TE2000 inverted microscope, eC1 confocal system (Nikon), with two laser lines (λ = 488 nm and 543 nm); optical tweezers induced by a 5 W ytterbium fiber continuous wave laser (λ > 1070 nm; IPG GmBH Germany)			an example of a confocal microscopy system equipped with optical tweezers
micromanipulators		n/a
borosilicate capillaries (with internal and external radii of 0.78 mm and 1 mm, respectively)	Harvard apparatus	30-0036
micropipette puller	Sutter Instrument	P-2100
microforge	Narishige	MF-800
piezoelectric actuator	Physik Instrumente	n/a
polystyrene streptavidin coated beads (diameter 3.2 µm)	Spherotech	SVP-30-5