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Journal articles on the topic 'GUVs'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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1

Mushenheim, Peter C., Joel S. Pendery, Douglas B. Weibel, Saverio E. Spagnolie, and Nicholas L. Abbott. "Straining soft colloids in aqueous nematic liquid crystals." Proceedings of the National Academy of Sciences 113, no. 20 (2016): 5564–69. http://dx.doi.org/10.1073/pnas.1600836113.

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Liquid crystals (LCs), because of their long-range molecular ordering, are anisotropic, elastic fluids. Herein, we report that elastic stresses imparted by nematic LCs can dynamically shape soft colloids and tune their physical properties. Specifically, we use giant unilamellar vesicles (GUVs) as soft colloids and explore the interplay of mechanical strain when the GUVs are confined within aqueous chromonic LC phases. Accompanying thermal quenching from isotropic to LC phases, we observe the elasticity of the LC phases to transform initially spherical GUVs (diameters of 2–50 µm) into two disti

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2

Carvalho, Denise, Ana Rodrigues, Vera Faustino, Diana Pinho, Elisabete Castanheira, and Rui Lima. "Microfluidic Deformability Study of an Innovative Blood Analogue Fluid Based on Giant Unilamellar Vesicles." Journal of Functional Biomaterials 9, no. 4 (2018): 70. http://dx.doi.org/10.3390/jfb9040070.

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Blood analogues have long been a topic of interest in biofluid mechanics due to the safety and ethical issues involved in the collection and handling of blood samples. Although the current blood analogue fluids can adequately mimic the rheological properties of blood from a macroscopic point of view, at the microscopic level blood analogues need further development and improvement. In this work, an innovative blood analogue containing giant unilamellar vesicles (GUVs) was developed to mimic the flow behavior of red blood cells (RBCs). A natural lipid mixture, soybean lecithin, was used for the

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3

Garten, Matthias, Lars D. Mosgaard, Thomas Bornschlögl, Stéphane Dieudonné, Patricia Bassereau, and Gilman E. S. Toombes. "Whole-GUV patch-clamping." Proceedings of the National Academy of Sciences 114, no. 2 (2016): 328–33. http://dx.doi.org/10.1073/pnas.1609142114.

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Studying how the membrane modulates ion channel and transporter activity is challenging because cells actively regulate membrane properties, whereas existing in vitro systems have limitations, such as residual solvent and unphysiologically high membrane tension. Cell-sized giant unilamellar vesicles (GUVs) would be ideal for in vitro electrophysiology, but efforts to measure the membrane current of intact GUVs have been unsuccessful. In this work, two challenges for obtaining the “whole-GUV” patch-clamp configuration were identified and resolved. First, unless the patch pipette and GUV pressur

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4

Souissi, Mariem, Julien Pernier, Olivier Rossier, et al. "Integrin-Functionalised Giant Unilamellar Vesicles via Gel-Assisted Formation: Good Practices and Pitfalls." International Journal of Molecular Sciences 22, no. 12 (2021): 6335. http://dx.doi.org/10.3390/ijms22126335.

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Giant unilamellar vesicles (GUV) are powerful tools to explore physics and biochemistry of the cell membrane in controlled conditions. For example, GUVs were extensively used to probe cell adhesion, but often using non-physiological linkers, due to the difficulty of incorporating transmembrane adhesion proteins into model membranes. Here we describe a new protocol for making GUVs incorporating the transmembrane protein integrin using gel-assisted swelling. We report an optimised protocol, enumerating the pitfalls encountered and precautions to be taken to maintain the robustness of the protoco

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5

Sych, Taras, Thomas Schubert, Romain Vauchelles, et al. "GUV-AP: multifunctional FIJI-based tool for quantitative image analysis of Giant Unilamellar Vesicles." Bioinformatics 35, no. 13 (2018): 2340–42. http://dx.doi.org/10.1093/bioinformatics/bty962.

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Abstract Motivation Giant Unilamellar Vesicles (GUVs) are widely used synthetic membrane systems that mimic native membranes and cellular processes. Various fluorescence imaging techniques can be employed for their characterization. In order to guarantee a fast and unbiased analysis of imaging data, the development of automated recognition and processing steps is required. Results We developed a fast and versatile Fiji-based macro for the analysis of digital microscopy images of GUVs. This macro was designed to investigate membrane dye incorporation and protein binding to membranes. Moreover,

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6

Litschel, Thomas, and Petra Schwille. "Protein Reconstitution Inside Giant Unilamellar Vesicles." Annual Review of Biophysics 50, no. 1 (2021): 525–48. http://dx.doi.org/10.1146/annurev-biophys-100620-114132.

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Giant unilamellar vesicles (GUVs) have gained great popularity as mimicries for cellular membranes. As their sizes are comfortably above the optical resolution limit, and their lipid composition is easily controlled, they are ideal for quantitative light microscopic investigation of dynamic processes in and on membranes. However, reconstitution of functional proteins into the lumen or the GUV membrane itself has proven technically challenging. In recent years, a selection of techniques has been introduced that tremendously improve GUV-assay development and enable the precise investigation of p

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7

Karal, Mohammad Abu Sayem, Tawfika Nasrin, Marzuk Ahmed, et al. "A new purification technique to obtain specific size distribution of giant lipid vesicles using dual filtration." PLOS ONE 16, no. 7 (2021): e0254930. http://dx.doi.org/10.1371/journal.pone.0254930.

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A new purification technique is developed for obtaining distribution of giant unilamellar vesicles (GUVs) within a specific range of sizes using dual filtration. The GUVs were prepared using well known natural swelling method. For filtration, different combinations of polycarbonate membranes were implemented in filter holders. In our experiment, the combinations of membranes were selected with corresponding pore sizes–(i) 12 and 10 μm, (ii) 12 and 8 μm, and (iii) 10 and 8 μm. By these filtration arrangements, obtained GUVs size distribution were in the ranges of 6−26 μm, 5–38 μm and 5–30 μm, r

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8

Gaul, Vinnie, Sergio G. Lopez, Barry R. Lentz, Niamh Moran, Robert J. Forster та Tia E. Keyes. "The lateral diffusion and fibrinogen induced clustering of platelet integrin αIIbβ3 reconstituted into physiologically mimetic GUVs". Integrative Biology 7, № 4 (2015): 402–11. http://dx.doi.org/10.1039/c5ib00003c.

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A novel method for reconstitution of Integrin α<sub>IIb</sub>β<sub>3</sub> into GUVs with unrestricted lipid composition is described and the lateral diffusion and phase partitioning of the integrin on activation and ligand binding in biomimetic GUVs compositions is studied in GUVs with biomimetic formulations.

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9

Sarkar, Malay Kumar, Mohammad Abu Sayem Karal, Marzuk Ahmed, et al. "Effects of osmotic pressure on the irreversible electroporation in giant lipid vesicles." PLOS ONE 16, no. 5 (2021): e0251690. http://dx.doi.org/10.1371/journal.pone.0251690.

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Irreversible electroporation (IRE) is a nonthermal tumor/cell ablation technique in which a series of high-voltage short pulses are used. As a new approach, we aimed to investigate the rupture of giant unilamellar vesicles (GUVs) using the IRE technique under different osmotic pressures (Π), and estimated the membrane tension due to Π. Two categories of GUVs were used in this study. One was prepared with a mixture of dioleoylphosphatidylglycerol (DOPG), dioleoylphosphatidylcholine (DOPC) and cholesterol (chol) for obtaining more biological relevance while other with a mixture of DOPG and DOPC,

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10

Jennings, Christopher S., Jeremy S. Rossman, Braeden A. Hourihan, Ross J. Marshall, Ross S. Forgan, and Barry A. Blight. "Immobilising giant unilamellar vesicles with zirconium metal–organic framework anchors." Soft Matter 17, no. 8 (2021): 2024–27. http://dx.doi.org/10.1039/d0sm02188a.

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A straightforward procedure for immobilising giant unilamellar vesicles (GUVs) using zircomium metal-organic frameworks as the anchroing medium is presented. Using this method GUVs can be immoblised and visualised for hours.

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11

Yandrapalli, Naresh, Tina Seemann, and Tom Robinson. "On-Chip Inverted Emulsion Method for Fast Giant Vesicle Production, Handling, and Analysis." Micromachines 11, no. 3 (2020): 285. http://dx.doi.org/10.3390/mi11030285.

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Liposomes and giant unilamellar vesicles (GUVs) in particular are excellent compartments for constructing artificial cells. Traditionally, their use requires bench-top vesicle growth, followed by experimentation under a microscope. Such steps are time-consuming and can lead to loss of vesicles when they are transferred to an observation chamber. To overcome these issues, we present an integrated microfluidic chip which combines GUV formation, trapping, and multiple separate experiments in the same device. First, we optimized the buffer conditions to maximize both the yield and the subsequent t

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12

Mora, Nestor Lopez, Yue Gao, M. Gertrude Gutierrez, et al. "Evaluation of dextran(ethylene glycol) hydrogel films for giant unilamellar lipid vesicle production and their application for the encapsulation of polymersomes." Soft Matter 13, no. 33 (2017): 5580–88. http://dx.doi.org/10.1039/c7sm00551b.

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13

Wiemann, Jared T., Zhiqiang Shen, Huilin Ye, Ying Li, and Yan Yu. "Membrane poration, wrinkling, and compression: deformations of lipid vesicles induced by amphiphilic Janus nanoparticles." Nanoscale 12, no. 39 (2020): 20326–36. http://dx.doi.org/10.1039/d0nr05355d.

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14

Lefrançois, Pauline, Bertrand Goudeau, and Stéphane Arbault. "Electroformation of phospholipid giant unilamellar vesicles in physiological phosphate buffer." Integrative Biology 10, no. 7 (2018): 429–34. http://dx.doi.org/10.1039/c8ib00074c.

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15

Chakraborty, T., S. M. Bartelt, J. Steinkühler, R. Dimova, and S. V. Wegner. "Light controlled cell-to-cell adhesion and chemical communication in minimal synthetic cells." Chemical Communications 55, no. 64 (2019): 9448–51. http://dx.doi.org/10.1039/c9cc04768a.

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16

Bartelt, S. M., E. Chervyachkova, J. Steinkühler, et al. "Dynamic blue light-switchable protein patterns on giant unilamellar vesicles." Chemical Communications 54, no. 8 (2018): 948–51. http://dx.doi.org/10.1039/c7cc08758f.

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17

Sobrinos-Sanguino, Marta, Silvia Zorrilla, Christine D. Keating, Begoña Monterroso, and Germán Rivas. "Encapsulation of a compartmentalized cytoplasm mimic within a lipid membrane by microfluidics." Chemical Communications 53, no. 35 (2017): 4775–78. http://dx.doi.org/10.1039/c7cc01289f.

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18

Maktabi, Sepehr, Jeffrey W. Schertzer, and Paul R. Chiarot. "Dewetting-induced formation and mechanical properties of synthetic bacterial outer membrane models (GUVs) with controlled inner-leaflet lipid composition." Soft Matter 15, no. 19 (2019): 3938–48. http://dx.doi.org/10.1039/c9sm00223e.

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19

Oka, M., T. Tanaka, S. Furuike, and M. Yamazaki. "Physical Properties of GUVs containing PEG-lipids." Seibutsu Butsuri 39, supplement (1999): S97. http://dx.doi.org/10.2142/biophys.39.s97_1.

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20

Bąk, Krzysztof M., Bartjan van Kolck, Krystyna Maslowska-Jarzyna, Panagiota Papadopoulou, Alexander Kros, and Michał J. Chmielewski. "Oxyanion transport across lipid bilayers: direct measurements in large and giant unilamellar vesicles." Chemical Communications 56, no. 36 (2020): 4910–13. http://dx.doi.org/10.1039/c9cc09888g.

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21

Haller, Barbara, Kerstin Göpfrich, Martin Schröter, Jan-Willi Janiesch, Ilia Platzman, and Joachim P. Spatz. "Charge-controlled microfluidic formation of lipid-based single- and multicompartment systems." Lab on a Chip 18, no. 17 (2018): 2665–74. http://dx.doi.org/10.1039/c8lc00582f.

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22

Witt, Hannes, Marian Vache, Andrea Cordes, and Andreas Janshoff. "Detachment of giant liposomes – coupling of receptor mobility and membrane shape." Soft Matter 16, no. 27 (2020): 6424–33. http://dx.doi.org/10.1039/d0sm00863j.

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We combine detachment experiments of giant unilamellar vesicles (GUVs) and membrane coated glass beads with theoretical considerations to study the impact of receptor mobility of adhesive glycolipids.

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23

Faizi, Hammad A., Shelli L. Frey, Jan Steinkühler, Rumiana Dimova, and Petia M. Vlahovska. "Bending rigidity of charged lipid bilayer membranes." Soft Matter 15, no. 29 (2019): 6006–13. http://dx.doi.org/10.1039/c9sm00772e.

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24

Olety, Balaji, Sarah L. Veatch та Akira Ono. "Phosphatidylinositol-(4,5)-Bisphosphate Acyl Chains Differentiate Membrane Binding of HIV-1 Gag from That of the Phospholipase Cδ1 Pleckstrin Homology Domain". Journal of Virology 89, № 15 (2015): 7861–73. http://dx.doi.org/10.1128/jvi.00794-15.

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ABSTRACTHIV-1 Gag, which drives virion assembly, interacts with a plasma membrane (PM)-specific phosphoinositide, phosphatidylinositol-(4,5)-bisphosphate [PI(4,5)P2]. While cellular acidic phospholipid-binding proteins/domains, such as the PI(4,5)P2-specific pleckstrin homology domain of phospholipase Cδ1 (PHPLCδ1), mediate headgroup-specific interactions with corresponding phospholipids, the exact nature of the Gag-PI(4,5)P2interaction remains undetermined. In this study, we used giant unilamellar vesicles (GUVs) to examine how PI(4,5)P2with unsaturated or saturated acyl chains affect membran

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25

Mora, Nestor Lopez, Azadeh Bahreman, Hennie Valkenier, et al. "Targeted anion transporter delivery by coiled-coil driven membrane fusion." Chemical Science 7, no. 3 (2016): 1768–72. http://dx.doi.org/10.1039/c5sc04282h.

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26

Ikeda, Atsushi, Tomohiro Hida, Tatsuya Iizuka, Manami Tsukamoto, Jun-ichi Kikuchi, and Kazuma Yasuhara. "Dynamic behaviour of giant unilamellar vesicles induced by the uptake of [70]fullerene." Chem. Commun. 50, no. 11 (2014): 1288–91. http://dx.doi.org/10.1039/c3cc47711h.

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27

Bao, Peng, Daniel A. Paterson, Sally A. Peyman, et al. "Production of giant unilamellar vesicles and encapsulation of lyotropic nematic liquid crystals." Soft Matter 17, no. 8 (2021): 2234–41. http://dx.doi.org/10.1039/d0sm01684e.

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We describe a modified microfluidic method for making Giant Unilamellar Vesicles (GUVs) via water/octanol-lipid/water double emulsion droplets and encapsulation of nematic lyotropic liquid crystals (LNLCs).

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28

Wang, Xuejing, Liangfei Tian, Hang Du, et al. "Chemical communication in spatially organized protocell colonies and protocell/living cell micro-arrays." Chemical Science 10, no. 41 (2019): 9446–53. http://dx.doi.org/10.1039/c9sc04522h.

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Arrays of giant unilamellar vesicles (GUVs) with controllable geometries and occupancies are prepared by acoustic trapping and used to implement chemical signaling in protocell colonies and protocell/living cell consortia.

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29

Karamdad, K., R. V. Law, J. M. Seddon, N. J. Brooks, and O. Ces. "Studying the effects of asymmetry on the bending rigidity of lipid membranes formed by microfluidics." Chemical Communications 52, no. 30 (2016): 5277–80. http://dx.doi.org/10.1039/c5cc10307j.

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In this article we detail a robust high-throughput microfluidic platform capable of fabricating either symmetric or asymmetric giant unilamellar vesicles (GUVs) and characterise the mechanical properties of their membranes.

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30

Zartner, Luisa, Moritz S. Muthwill, Ionel Adrian Dinu, Cora-Ann Schoenenberger, and Cornelia G. Palivan. "The rise of bio-inspired polymer compartments responding to pathology-related signals." Journal of Materials Chemistry B 8, no. 29 (2020): 6252–70. http://dx.doi.org/10.1039/d0tb00475h.

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Self-organized nano- and microscale polymer compartments such as polymersomes, giant unilamellar vesicles (GUVs), polyion complex vesicles (PICsomes) and layer-by-layer (LbL) capsules have increasing potential in many sensing applications.

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31

Sarmento, M. J., S. N. Pinto, A. Coutinho, M. Prieto, and F. Fernandes. "Accurate quantification of inter-domain partition coefficients in GUVs exhibiting lipid phase coexistence." RSC Advances 6, no. 71 (2016): 66641–49. http://dx.doi.org/10.1039/c6ra13170k.

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Giant unilamellar vesicles (GUVs) with phase coexistence allow for the recovery of inter-domain partition coefficients (K<sub>p</sub>) of fluorescent molecules through comparison of fluorescence intensities in each phase.

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32

Sachdev, Shaurya, Aswin Muralidharan, Dipendra K. Choudhary, et al. "DNA translocation to giant unilamellar vesicles during electroporation is independent of DNA size." Soft Matter 15, no. 45 (2019): 9187–94. http://dx.doi.org/10.1039/c9sm01274e.

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DNA delivery into GUVs during electroporation is governed by bulk electrophoretic mobility implying a mechanism in which DNA molecules enter in their coiled conformation, as opposed to stochastic threading, through electro-pores.

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33

Vallejo, D., S. H. Lee, D. Lee, et al. "Cell-sized lipid vesicles for cell-cell synaptic therapies." TECHNOLOGY 05, no. 04 (2017): 201–13. http://dx.doi.org/10.1142/s233954781750011x.

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Cell-sized lipid vesicles (CLVs) have shown great promise for therapeutic and artificial cell applications, but their fragility and short shelf life has hindered widespread adoption and commercial viability. We present a method to circumvent the storage limitations of CLVs such as giant unilamellar vesicles (GUVs) and single-compartment multisomes (SCMs) by storing them in a double emulsion precursor form. The double emulsions can be stored for at least 8 months and readily converted into either GUVs or SCMs at any time. In this study, we investigate the interfacial parameters responsible for

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34

Tanaka, T., Y. Yamashita, M. Oka, and M. Yamazaki. "Physical Properties of GUVs containing PEG-lipids (3)." Seibutsu Butsuri 40, supplement (2000): S149. http://dx.doi.org/10.2142/biophys.40.s149_4.

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35

Balleza, Daniel, Andrea Mescola, Nathaly Marín–Medina, et al. "Complex Phase Behavior of GUVs Containing Different Sphingomyelins." Biophysical Journal 116, no. 3 (2019): 503–17. http://dx.doi.org/10.1016/j.bpj.2018.12.018.

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36

Lopez Mora, Nestor, Heather Findlay, and Paula Booth. "Evaluating Bilayer Mechanical Properties in Protein Reconstituted GUVs." Biophysical Journal 112, no. 3 (2017): 75a—76a. http://dx.doi.org/10.1016/j.bpj.2016.11.454.

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37

O' Connor, Darragh, Aisling Byrne, and Tia E. Keyes. "Linker length in fluorophore–cholesterol conjugates directs phase selectivity and cellular localisation in GUVs and live cells." RSC Advances 9, no. 40 (2019): 22805–16. http://dx.doi.org/10.1039/c9ra03905h.

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By inserting a hexyl linker between a BODIPY probe and cholesterol pendant, the localization of the probe at ternary phase separated GUVs switches from L<sub>d</sub> to L<sub>o</sub> domains with high specificity.

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38

Rideau, Emeline, Frederik R. Wurm, and Katharina Landfester. "Giant polymersomes from non-assisted film hydration of phosphate-based block copolymers." Polymer Chemistry 9, no. 44 (2018): 5385–94. http://dx.doi.org/10.1039/c8py00992a.

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Polybutadiene-block-poly(ethyl ethylene phosphate) can reproducibly self-assemble in large number into giant unilamellar vesicles (GUVs) by non-assisted film hydration, representing a stepping stone for better liposomes – substitutes towards the generation of artificial cells.

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39

Chang, Chunmei, Xiaoshan Shi, Liv E. Jensen, et al. "Reconstitution of cargo-induced LC3 lipidation in mammalian selective autophagy." Science Advances 7, no. 17 (2021): eabg4922. http://dx.doi.org/10.1126/sciadv.abg4922.

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Selective autophagy of damaged mitochondria, protein aggregates, and other cargoes is essential for health. Cargo initiates phagophore biogenesis, which entails the conjugation of LC3 to phosphatidylethanolamine. Current models suggest that clustered ubiquitin chains on a cargo trigger a cascade from autophagic cargo receptors through the core complexes ULK1 and class III phosphatidylinositol 3-kinase complex I, WIPI2, and the ATG7, ATG3, and ATG12ATG5-ATG16L1 machinery of LC3 lipidation. This was tested using giant unilamellar vesicles (GUVs), GST-Ub4 as a model cargo, the cargo receptors NDP

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40

Pennington, Edward Ross, E. Madison Sullivan, Amy Fix, et al. "Proteolipid domains form in biomimetic and cardiac mitochondrial vesicles and are regulated by cardiolipin concentration but not monolyso-cardiolipin." Journal of Biological Chemistry 293, no. 41 (2018): 15933–46. http://dx.doi.org/10.1074/jbc.ra118.004948.

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Cardiolipin (CL) is an anionic phospholipid mainly located in the inner mitochondrial membrane, where it helps regulate bioenergetics, membrane structure, and apoptosis. Localized, phase-segregated domains of CL are hypothesized to control mitochondrial inner membrane organization. However, the existence and underlying mechanisms regulating these mitochondrial domains are unclear. Here, we first isolated detergent-resistant cardiac mitochondrial membranes that have been reported to be CL-enriched domains. Experiments with different detergents yielded only nonspecific solubilization of mitochon

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41

Omidvar, Ramin, and Winfried Römer. "Glycan-decorated protocells: novel features for rebuilding cellular processes." Interface Focus 9, no. 2 (2019): 20180084. http://dx.doi.org/10.1098/rsfs.2018.0084.

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In synthetic biology approaches, lipid vesicles are widely used as protocell models. While many compounds have been encapsulated in vesicles (e.g. DNA, cytoskeleton and enzymes), the incorporation of glycocalyx components in the lipid bilayer has attracted much less attention so far. In recent years, glycoconjugates have been integrated in the membrane of giant unilamellar vesicles (GUVs). These minimal membrane systems have largely contributed to shed light on the molecular mechanisms of cellular processes. In this review, we first introduce several preparation and biophysical characterizatio

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42

Ebenhan, Jan, Stefan Werner, Matthias Schulz, Wolfgang Binder, and Kirsten Bacia. "Investigation of Hybrid Lipid-Polymer GUVs by Fluorescence Correlation Spectroscopy." Biophysical Journal 106, no. 2 (2014): 603a. http://dx.doi.org/10.1016/j.bpj.2013.11.3339.

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43

Yoshitain, Takuya, and Masahito Yamazaki. "2P275 Water permeability of lipid membranes of GUVs and its dependence on actin cytoskeletons inside the GUVs(Native and artificial biomembranes-dynamics,Poster Presentations)." Seibutsu Butsuri 47, supplement (2007): S181. http://dx.doi.org/10.2142/biophys.47.s181_4.

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44

Suarez, Ivan A. Rey, Guillaume Gay, Alexander Ladino, Andres Gonzalez Mancera, and Chad Leidy. "Dynamics of Sedimentation and Deformation of GUVs Under Different Tonicity Conditions." Biophysical Journal 98, no. 3 (2010): 491a. http://dx.doi.org/10.1016/j.bpj.2009.12.2675.

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45

Ghazaryan, Narine. "Behavior of Proteolipid GUVs formed in Macrovipera Lebetina Obtusa Venom Solution." Biophysical Journal 104, no. 2 (2013): 86a. http://dx.doi.org/10.1016/j.bpj.2012.11.519.

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46

Chiantia, Salvatore, Petra Schwille, Andrey S. Klymchenko та Erwin London. "Asymmetric GUVs Prepared by MβCD-Mediated Lipid Exchange: An FCS Study". Biophysical Journal 100, № 1 (2011): L1—L3. http://dx.doi.org/10.1016/j.bpj.2010.11.051.

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47

Faizi, Hammad A., Rumiana Dimova, and Petia M. Vlahovska. "Transient Electrodeformation of Giant Unilamellar Vesicles (GUVS) to Probe Membrane Viscosity." Biophysical Journal 118, no. 3 (2020): 322a. http://dx.doi.org/10.1016/j.bpj.2019.11.1808.

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48

Saga, Yuko, Yasuyuki Inaoka, and Masahito Yamazaki. "2P-230 Oleic Acid-Induced Growth and Shape Changes of Single DOPC-GUVs and DPPC/chol-GUVs(The 46th Annual Meeting of the Biophysical Society of Japan)." Seibutsu Butsuri 48, supplement (2008): S110. http://dx.doi.org/10.2142/biophys.48.s110_4.

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49

Esquembre, Rocío, Sandra N. Pinto, José Antonio Poveda, Manuel Prieto, and C. Reyes Mateo. "Immobilization and characterization of giant unilamellar vesicles (GUVs) within porous silica glasses." Soft Matter 8, no. 2 (2012): 408–17. http://dx.doi.org/10.1039/c1sm06264f.

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50

Mauroy, Chloé, Pauline Castagnos, Marie-Claire Blache, et al. "Interaction between GUVs and catanionic nanocontainers: new insight into spontaneous membrane fusion." Chemical Communications 48, no. 53 (2012): 6648. http://dx.doi.org/10.1039/c2cc32093b.

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