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10.5: Working with Lipids

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    NIH_NCBI_iCn3D_Banner.svg Figure \(\PageIndex{x}\): Hxxxx (xxxx) (Copyright; author via source).
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    Introduction

    Lipid, although small compared to large biopolymers like proteins, nucleic acid and large glycans, are very heterogenous in structure, given the large array of fatty acid and isoprenoid chain lengths, numbers of double bonds, etc that appear in different lipid classes. In addition to analyzing lipid structure, lipids are used in the laboratory to create liposomes (vesicles), which serve as models for membrane bilayers and for encapsulation of chemical species (drugs, vacccine) for medical use and for solubilization of membrane proteins. In this section we will concentrate on the creation of lipid vesicles (critical for the encapsulation of RNA vaccines against the SARS CoV-2 spike protein) and the chemical analysis of biological lipids, whose composition affects health and disease states.

    Liposomes

    Liposomes produced in the lab can be unilamellar, consisting of a single bilayer surrounding the internal aqueous compartment, or multilamellar, consisting of multiple bilayers surrounding the enclosed aqueous solution. You can image the multilamellar vesicles resembles an onion with its multiple layers. Cartoons of unilamellar and multilamellar liposomes are shown in Figure \(\PageIndex{1}\) below, where each concentric circle represents a bilayer.

    liposomeonion.jpg
    Figure \(\PageIndex{1}\): Cartoons of unilamellar and multilamellar liposomes (each concentric circle represents a bilayer)

    Liposomes vary in diameter. They can be generally categorized into small (S, diameter < 25 nm), intermediate (I, diameter around 100 nm), and large (L, diameter from 250-1000 nm). If these vesicles are unilamellar, they are abbreviated as SUV, IUV, and LUV, respectively. Their various sizes are shown in Table \(\PageIndex{1}\) below, in comparison to other large biological structures.

    liposize

    Table \(\PageIndex{1}\): Sizes of liposomes/vesicles compared to other biological structures

    The chemical composition of liposomes can be widely varied. Most contain neutral phospholipids like phosphatidyl choline (PC), phosphatidyl ethanolamine (PE), or sphingomyelin (SM), supplemented, if desired, with negatively charged phospholipids, like phosphatidyl serine (PS) and phosphatidyl glycerol (PG). In addition, single chain amphiphiles like cholesterol (C) and detergents can be incorporated into the bilayer membrane, which modulates the fluidity and transition temperature (Tm) of the bilayer. If present in too great a concentration, single chain amphiphiles like detergents, which form micelles, can disrupt the membrane so completely that the double chain amphiphiles become incorporated into detergent micelles, now called mixed micelles, in a process which effectively destroys the membrane bilayer.

    Given the large degree of unsaturation at C2, what do you expect the transition temperature of a liposome composed only of egg yolk PC to be? (Vesicles made using more saturated PC from mammalian sources have Tm of around 40oC.) This high degree of unsaturation makes egg yolk PC very susceptible to oxidation, which could alter the properties of the liposome dramatically. Synthetic PC made with saturated fatty acids could alleviate that problem.

    The properties of liposomes (charge density, membrane fluidity, and permeability) are determined by the lipid composition and size of the vesicle. The desired properties will be, in turn, determined by the use of the particular liposome. The vesicles offer wonderful, simple models to study the biochemistry and biophysics of natural membranes. In fact, membrane proteins can actually be incorporated into the liposome bilayer using the exact method you will be using. But apart from these purposes, liposomes can be used to encapsulate water soluble molecules such as nucleic acids, proteins, and toxic drugs. These liposomes can be targeted to specific cells if antibodies or other molecules which will bind specifically to the target cell can be incorporated into the bilayer of the vesicle. Intraliposomal material may then be transferred into the cell either by fusion of the vesicle with the cell, or by endocytosis of the vesicle.

    Since phospholipids will spontaneously form some type of bilayer structure when placed in water, most efforts in liposome production involve producing vesicles with the desired size, lamellar structure, and physical characteristics, which as previously stated is controlled both by liposome size and chemical composition. Also, ways must be developed to entrap the desired molecule inside the vesicle in the most cost-effective manner, and with minimal leaking of contents. All methods of production involve four steps: 1) drying of organic solvent-solubilized lipids; 2) dispersion of the lipids in the appropriate aqueous solution; 3) separation of liposome from excess starting reagents; and 4) characterization of the vesicles for chemical composition, Tm, permeability, size, etc.

    1. Drying of lipids:

    Purified lipids of the desired composition (often times egg PC:cholesterol:PS in molar ratios of 0.9:1.0:0.1) are dissolved in a purified, water-free organic solvent mixture (often chloroform/methanol, 2:1 v/v) and dried down in a round bottom flask on a rotary evaporator under reduced pressure (using a water aspirator) and slightly elevated temperature (20-40oC). The rapid rotation of the flask will ensure that the lipid is dispersed over a large surface area, and will increase the rate of evaporation. To remove the last traces of solvent, the dried flask is usually placed under a high vacuum overnight. If a small volume (< 1 ml) of lipid solution is used,, the solvent can be evaporated under a stream of nitrogen. To avoid entrapment of residual chloroform in the lipid film, the film is dissolved in t-butyl-methylether diethyl ether , and dried several times. Alternatively, the residual solvent can be removed under high vacuum.

    2. Dispersion of the lipids in the appropriate aqueous solution:

    There are three main methods of dispersing the lipids into an aqueous solution to form liposomes.

    a. mechanical dispersion - in this method, lipid dried onto the inside glass surface of a container is hydrated with an aqueous solution, which literally peals off the lipid to form multilamellar - MLV - (multiple bilayers separated by water) vesicles. Only a small part of the aqueous solution is encapsulated inside the liposome, so this is not the method of choice for the encapsulation of expensive or rather insoluble solutes. Depending on the degree of agitation and the nature of the lipid used, different sized liposomes can be prepared.

    b. organic solvent dispersion - In these methods, the lipids, which are dissolved in organic solvents, are injected through a fine needle, at a slow rate, into an aqueous solution in which the organic solvent may be miscible (such as ethanol) or immiscible (such as ether). In each case, the lipids orient at the interface between the organic solvent and aqueous solution, to form bilayer structures. Injection of ethanol-dissolved lipids provides a simple way to produce SUV, but because liposome formation can not occur at an ethanol concentration greater than 7.5%, only a fraction of the total aqueous phase can be entrapped in the vesicle; hence this technique is not cost-effective for entrapment of an expensive solute. Alternatively, the lipid can be dissolved in ether and slowly injected into an aqueous solution which is warmed so that the ether evaporates at the rate at which it is injected. Since the ether is volatilized, large amounts of lipid can be introduced and encapsulation efficiency of the aqueous solution is high.

    c. detergent dispersion and solubilization - In this method, lipids are solubilized in an aqueous solution through the addition of detergents. The detergents are removed slowly from the solution, resulting in the spontaneous formation of liposomes. Detergents are single chain amphiphiles that spontaneously form micelles in aqueous solution when the concentration of free lipid rises to a minimum critical value, the critical micelle concentration (CMC); at this concentration, self-association of detergent results in the formation of a stable aggregate, the micelle. This is illustrated in Figure \(\PageIndex{2}\) below.

    monomermicellphase.gif
    Figure \(\PageIndex{2}\): [Single chain amphiphile] in solution vs [Single chain amphiphile] added - the CMC

    Table \(\PageIndex{2}\) below shows the properties and CMC of various detergents.

    Table \(\PageIndex{2}\): Properties and CMC of various detergents (data from Avanti Polar Lipids)
    Name mM mg/ml MW
    n-hepty glucopyranoside 70 19.5 278
    n-octyl glucopyranoside 23.2 6.8 292
    n-nonyl glucopyranoside 6.5 2.0 306
    n-decyl maltoside 2.19 1.1 499
    n-dodecyl maltotrioside 0.2 0.16 825
    Triton X-100 (a) 0.24 0.15 625
    Nonidet P-40 (b) 0.29 0.02 603
    Tween 20 (c) 0.033 0.04 1364
    Brij 98 (d) 0.025 0.04 1527
    sodium deoxycholate 2-6 1.7 415
    sodium taurocholate 10-15 6.7 538
    sodium cholate 14 6.0 431
    sodium dodecyl sulfate 8.3 2.4 289

    Making liposomes by dialysis

    Lipids are deposited in a small container. An aqueous solution is then added, containing water-soluble molecules for encapsulation. Detergent is then added at a concentration in excess of the lipid concentration and greater than its CMC. The lipid molecules are then "emulsified" in the detergent micelle. The solubilized mixture is then placed in a semi-permeable dialysis bag, which is placed in a large volume of an aqueous solution. The free detergent in solution is in equilibrium with the detergent in the micelle. The bag contains microscopic holes large enough for the monomeric detergent molecule to pass through, but small enough so that the large micelle can not. The lipid, during this process, is embedded in the micelle forming a detergent-lipid mixed micelle. As dialysis continues, the monomeric detergent partitions throughout both the volume in the bag and the volume surrounding the bag, while the mixed micelle remains in the bag. If the aqueous solution surrounding the bag is changed several times with fresh solution, the equilibrium in the bag is shifted to the monomeric form. Alternatively, detergent-adsorbing beads (such as Bio Bead SM-2 by Bio-Rad) can be placed in the aqueous solution surrounding the bag to speed up the process of detergent reequilibration. Eventually, all the detergent is in this form, and during the process, which occurs slowly, the lipid in the mixed micelle self-associates to form a liposome. A detergent of low monomer molecular weight and a high CMC is most desirable for this method of liposome production. Another method of removing the free detergent is through gel filtration chromatography. In this technique, molecules of disparate molecular weights can be separated from each other. An explanation follows this discussion. This method of formation of unilamellar liposomes is the method of choice if membrane proteins are to be inserted into the liposome bilayer for the purpose of targeting the liposome. It is not the best method, however, for quantitative encapsulation of expensive soluble molecules.

    Making Liposomes by Extrusion

    These multilamellar liposomes can be further processed to form unilamellar liposomes by several techniques. These include probe or bath sonication of the MLV, extrusion at high pressure of the MLV through membrane filters of defined pore size, or pH-induced vesiculation in which a transient change in pH destabilizes the MLV in favor of unilamellar liposomes. Another technique involves fusion of SUV by repeated freezing and thawing or by fusion of SUV containing acidic phospholipids (such as PS) through Ca2+ mediated aggregation.

    Figure \(\PageIndex{3}\): below show the structure of vesicles as they undergo multiple freeze/thaw cycles.

    LUV_ExtrusionPrepFinalA.svg
    Figure \(\PageIndex{3}\): Structure of multilamellar vesicles as they undergo multiple freeze/thaw cycles

    Figure \(\PageIndex{4}\) below shows the final step in making large unilamellar vesicles by extrusion of freeze/thaw intermediates.

    LUV_ExtrusionPrepFinalB.svg
    Figure \(\PageIndex{4}\): Conversion of multilamellar vesicles to unilamellar vesicles by extrusion

    Once the liposomes are formed, they must be separated from free monomeric lipid, detergent, and unencapsulated solutes. This can be done again by dialysis, or more readily by size exclusion chromatography. Macromolecules of different sizes can be separated on a column in which the stationary phase is a polymerized agarose or acrylamide bead, which contain pores of various sizes. A small molecule (such as monomer detergent, free lipid, or small aqueous solute) in the mobile phase (aqueous buffered solution) may enter the pores in the bead, while a larger macromolecule or aggregate (such as a large protein, a micelle, or a liposome) may not, due to size restriction. The result is that a larger fraction of the overall volume of the column is available to the smaller molecules, which thus spend a longer time on the column and are eluted by the mobile solvent after the larger species. Liposomes can be characterized both chemically, to determine the average lipid and protein (if they were incorporated) composition of the bilayer, and physically, to determine the size, permeability, lamellarity, and amount of encapsulated material. Size is usually determined by electron microscopy or indirectly by light scattering from these large species.

    Chemical Analysis of Lipids

    There are so many lipids and their derivatives that are so subtlety different that the most sensitive one are needed for separation and analysis. The field of lipodomics focus on the analyis of structure and function of all lipids in the cell. The most useful techniques are analysis (and separation) by gas chromatography (GC) followed by mass spectrometery (MS). NMR spectroscopy is also important. For GC analysis, the lipid must be made volatile, which limits its use in some circumstances. MS analysis is most senstive. MS requires ion formation, and techniques like electrospray ionization and matrix-assisted laser desorption/ionization (MALDI) are used.

    Gas chromatography

    (This section is adapted from https://www.intechopen.com/chapters/64008. Creative Commons Attribution 3.0 License). In GC, a gas is the mobile phase which carriers lipids through the stationary phase of the column. A cording to the principles of chromatographic techniques, the gas chromatography (GC) is applied when aimed to separate organic compounds from a mixture in the gas form. For this purpose, the GC uses interactions among the sample components and the stationary/mobile phases. After lipid extraction with chlorform and/or methanol, the samples (lipid mixture) are usually liquids and must be exposed to a high temperature at the gas chromatograph entrance (injector). Vaporized, the samples are carried by a gas, which is usually a nonheavy and inert gas (i.e., hydrogen, helium), through a long capillary column containing a high or low polarity material (stationary phase)

    The gaseous compounds generated from the vaporized sample interact with the stationary phase what allows each compound to elute/separate at a different time (retention time). Because GC considers both chemical and physical properties of the vaporized compounds, those with more chemical affinity to the stationary phase will take longer time to be removed from the column and the temperature will influence the overall process. This explains why the column stays in an oven, which is programmed to work at different temperature ranges (i.e., temperature programming) in which the compounds are carried out by the gas according to their boiling point until they get to an electronic detector.

    At the end of GC analysis, the electronic detector generates a chromatogram based on retention time by intensity. This allows a qualitative identification of the lipid compounds by comparing their retention times with certified standard using the flame ionization detector (FID) or by deduction of spectra information using a mass spectrometer as detector. Lipid quantification can also be performed using analytical procedures of external or internal certified standard in GC analysis..

    Main points to be considered when assessing FAs by GC analysis are the carrier gas flow rate, column length, and the temperature because these can influence the order or retention time of the lipid compounds and then must be precisely standardized. The column length of the stationary phase influences the resolution of the analytes, once the number of theoretical plates (hypothetical zone in which two phases establish an equilibrium with each other) is respectively high in longer column. As fat and oils have high boiling points not supported by the stationary phase, a previous derivatization reaction step is required after lipid extraction from the biological sample, in which triacylglycerol and free fatty acids are transformed into their respective free fatty esters with lower boiling points (transesterification/esterification reaction).. Several methods are available for FAs derivatization, and the most applied ones are described in the 969.33 AOAC’s method.

    Particularly for cholesterol analysis, the samples preparation must consider a derivatization reaction. This allows to block protic sites of steroids obtained after an unsaponifiable lipid extraction had been performed, and also, to diminish dipole-dipole interactions, to increase the volatility of the compounds, and to generate products with reduced polarity. Cholesterol derivatization is usually achieved by using trimethylsilyl compounds as reagents (silylation reaction). A common method for this purpose uses N,O-bis(trimethylsilyl-trifluoroacetamide/trimethylchlorosilane).

    Nowadays, other more modern analytical tools than GC (next-generation techniques) do not require sample derivatization for lipid analysis. Needed lipid derivatization can be then consider a quite limitation step of the technique. In comparison with next-generation techniques, GC also implies in using greater sample quantities. This may be the main limitation in biological assays, which usually lead with restricted sample amounts. Nevertheless, by using certified standard and a powerful detector as FID, GC has the advantage to allow a precise and complete (by burning every compound, no one is lost in the detection) quantification of lipid compounds from biological samples, not always achieved by the other analytical techniques. In this context, GC continues to be accepted as an efficient and simple technique for FA and sterol analyses, mainly when combined with mass spectrometry (MS, detailed later in this chapter).

    Mass spectrometry

    (This section is derived from https://doi.org/10.1038/s41467-019-14180-4. Creative Commons Attribution 4.0 International License: http://creativecommons.org/licenses/by/4.0/).

    Mass spectrometry (MS) has become the method of choice for lipid analysis, offering label-free detection at high sensitivity and structural characterization capability. However, large-scale lipid analysis with a comprehensive capability of revealing all levels of structure information still represents a significant analytical challenge for lipidomics. General protocols, for instance, have five levels in terms of structure information, including lipid class, fatty acyl identities, fatty acyl sn-positions, and C=C location/geometry (viz cis/trans) in the fatty acyl. Successful attempts for determining C=C locations in fatty acyls or their sn-positions have already been reported for MS analysis, enabling characterization of detailed structure moieties and identification of lipid structure isomers. An extremely useful feature offered by lipid isomer analysis, is the relative quantitation achieved at high precisions without requiring the use of lipid standards, which is not readily available. Remarkably, our recent study demonstrated close correlation between the lipid C=C location isomer compositions and Type II diabetes, which owes to a tighter regulation on lipid desaturation, allowing efficient elimination of interferences due to variations among samples"

    Various methods have been explored for differentiating the lipid C=C location and sn-position isomers. Ozone-induced dissociation (OzID) and ultraviolet photodissociation (UVPD) have been used to determine both sn-positions and C=C locations in GPs. By coupling the Paternò-Bǜchi (PB) photochemical reaction with tandem MS (MS/MS), qualitative and quantitative analysis of lipids with C=C specificity from complex biological samples can be accomplished. PB reaction converts the C=C to an oxetane which can be preferentially fragmented by low-energy collision-induced dissociation (CID).

    An ideal analytical tool for lipidomics in order to survey a wide range of lipids in discovery work should not only provide detailed information at multiple lipid structure isomer levels (e.g., C=C location/geometry and sn-position), but also be feasible for large-scale quantitative analysis. UVPD is capable of assigning C=C locations and sn-positions of fatty acyls, while OzID may be the only one that has been well demonstrated for assigning C=C locations in sn-specific fatty acyls. One problem of OzID is the long reaction time required for the ion trap implementation, however recent work has demonstrated the ability to perform OzID on LC-compatible time scales in the high pressure regions of the MS system. For PB reaction method, both shotgun analysis and HPLC-PB-MS/MS workflow have been developed for identifying a large number of C=C location isomers. Figure \(\PageIndex{5}\) below describes methods for the determination of C=C location and sn-isomers in lipids.

    LargeScaleLipidAnalysis_doublebondsandSN_Fig1-01.svg
    Figure \(\PageIndex{5}\): Mmethods for the determination of C=C location and sn-isomers in lipidsa The chemical structure of PC 18:1(9Z)/16:0. b Schematic of the experimental setup for online derivatization of unsaturated GPs by coupling 254 nm irradiation with nanoESI-MS. c MS spectrum of PC 16:0/18:1(9Z) after 30 s reaction. d MS3 spectrum of PC 16:0/18:1(9Z) without PB derivatization. Sodiated lipid precursors were first fragmented to generate product ions after headgroup loss (−183 Da). Product ion at m/z 599.5 was further fragmented to release sn-1-specific diagnostic ions at m/z 319 (C16:0) and 345 (C18:1). e Comparison the relative abundance of sn-position and C=C location specific ions of PC 16:0/18:1(9Z) without and with PB derivatization using different PB reagents (Bza: benzaldehyde, APh: acetophenone, BPh: benzophenone, AP: acetylpyridine). Error bar represents the standard deviation, n = 3. Cao, W., Cheng, S., Yang, J. et al. Large-scale lipid analysis with C=C location and sn-position isomer resolving power. Nat Commun 11, 375 (2020). https://doi.org/10.1038/s41467-019-14180-4. DOI: https://doi.org/10.1038/s41467-019-14180-4. Creative Commons Attribution 4.0 International License: http://creativecommons.org/licenses/by/4.0/.

    10.5: Working with Lipids is shared under a not declared license and was authored, remixed, and/or curated by Henry Jakubowski.

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