Literature DB >> 31428671

A Tunable Microfluidic Device Enables Cargo Encapsulation by Cell- or Organelle-Sized Lipid Vesicles Comprising Asymmetric Lipid Bilayers.

Valentin Romanov1, John McCullough2, Bruce K Gale1, Adam Frost3.   

Abstract

Cellular membranes play host to a wide variety of morphologically and chemically complex processes. Although model membranes, like liposomes, are already widely used to reconstitute and study these processes, better tools are needed for making model bilayers that faithfully mimic cellular membranes. Existing methods for fabricating cell-sized (μm) or organelle-sized (tens to hundreds of nanometers) lipid vesicles have distinctly different requirements. Of particular note for biology, it remains challenging for any technique to efficiently encapsulate fragile cargo molecules or to generate liposomes with stable, asymmetric lipid leaflets within the bilayer. Here a tunable microfluidic device and protocol for fabricating liposomes with desired diameters ranging from ≈10 μm to ≈100 nm are described. Lipid vesicle size is templated by the simple inclusion of a polycarbonate filter within the microfluidic system and tuned with flow rate. It is shown that the vesicles made with this device are stable, unilamellar, lipid asymmetric, and capable of supporting transmembrane protein assembly, peripheral membrane protein binding, as well as soluble cargo encapsulation (including designer nanocages for biotechnology applications). These fabricated vesicles provide a new platform for studying the biophysically rich processes found within lipid-lipid and lipid-protein systems typically associated with cellular membranes.

Entities:  

Keywords:  cross-flow emulsification; cryogenic electron microscopy (cryoEM); liposomes; microfluidics; phase transfer

Year:  2019        PMID: 31428671      PMCID: PMC6699779          DOI: 10.1002/adbi.201900010

Source DB:  PubMed          Journal:  Adv Biosyst        ISSN: 2366-7478


  39 in total

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Authors:  W Wang
Journal:  Int J Pharm       Date:  1999-08-20       Impact factor: 5.875

2.  Cloning, isolation and characterization of the Thermotoga maritima KDPG aldolase.

Authors:  Jennifer S Griffiths; Nathan J Wymer; Eugenia Njolito; S Niranjanakumari; Carol A Fierke; Eric J Toone
Journal:  Bioorg Med Chem       Date:  2002-03       Impact factor: 3.641

3.  Cryo-transmission electron microscopy of frozen-hydrated sections of Escherichia coli and Pseudomonas aeruginosa.

Authors:  Valério R F Matias; Ashraf Al-Amoudi; Jacques Dubochet; Terry J Beveridge
Journal:  J Bacteriol       Date:  2003-10       Impact factor: 3.490

4.  Controlled vesicle self-assembly in microfluidic channels with hydrodynamic focusing.

Authors:  Andreas Jahn; Wyatt N Vreeland; Michael Gaitan; Laurie E Locascio
Journal:  J Am Chem Soc       Date:  2004-03-10       Impact factor: 15.419

5.  The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B.

Authors:  Evan Reid; James Connell; Thomas L Edwards; Simon Duley; Stephanie E Brown; Christopher M Sanderson
Journal:  Hum Mol Genet       Date:  2004-11-10       Impact factor: 6.150

6.  A vesicle bioreactor as a step toward an artificial cell assembly.

Authors:  Vincent Noireaux; Albert Libchaber
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-10       Impact factor: 11.205

7.  Automated electron microscope tomography using robust prediction of specimen movements.

Authors:  David N Mastronarde
Journal:  J Struct Biol       Date:  2005-10       Impact factor: 2.867

8.  Adipophilin-enriched domains in the ER membrane are sites of lipid droplet biogenesis.

Authors:  Horst Robenek; Oliver Hofnagel; Insa Buers; Mirko J Robenek; David Troyer; Nicholas J Severs
Journal:  J Cell Sci       Date:  2006-09-19       Impact factor: 5.285

9.  Fluorescence assay for phospholipid membrane asymmetry.

Authors:  J C McIntyre; R G Sleight
Journal:  Biochemistry       Date:  1991-12-24       Impact factor: 3.162

10.  Pore formation by equinatoxin II, a eukaryotic protein toxin, occurs by induction of nonlamellar lipid structures.

Authors:  Gregor Anderluh; Mauro Dalla Serra; Gabriella Viero; Graziano Guella; Peter Macek; Gianfranco Menestrina
Journal:  J Biol Chem       Date:  2003-08-27       Impact factor: 5.157

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  1 in total

1.  Membrane constriction and thinning by sequential ESCRT-III polymerization.

Authors:  Henry C Nguyen; Nathaniel Talledge; John McCullough; Abhimanyu Sharma; Frank R Moss; Janet H Iwasa; Michael D Vershinin; Wesley I Sundquist; Adam Frost
Journal:  Nat Struct Mol Biol       Date:  2020-04-06       Impact factor: 15.369

  1 in total

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