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Osmotic Shock-Triggered Assembly of Highly Charged, Nanoparticle-Supported Membranes

  • Peter J. Chung
    Peter J. Chung
    James Franck Institute,  Department of Chemistry  and  Institute of Biophysical Dynamics, The University of Chicago, Chicago, Illinois 60637, United States
  • Hyeondo Luke Hwang
    Hyeondo Luke Hwang
    Department of Chemistry, The University of Chicago, Chicago, Illinois 60637, United States
  • Kinjal Dasbiswas
    Kinjal Dasbiswas
    James Franck Institute, The University of Chicago, Chicago, Illinois 60637, United States
  • Alessandra Leong
    Alessandra Leong
    Department of Chemistry, The University of Chicago, Chicago, Illinois 60637, United States
  • , and 
  • Ka Yee C. Lee*
    Ka Yee C. Lee
    James Franck Institute,  Department of Chemistry  and  Institute of Biophysical Dynamics, The University of Chicago, Chicago, Illinois 60637, United States
    *E-mail: [email protected]
Cite this: Langmuir 2018, 34, 43, 13000–13005
Publication Date (Web):October 10, 2018
https://doi.org/10.1021/acs.langmuir.8b03026
Copyright © 2018 American Chemical Society

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    Abstract

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    Spherical nanoparticle-supported lipid bilayers (SSLBs) combine precision nanoparticle engineering with biocompatible interfaces for various applications, ranging from drug delivery platforms to structural probes for membrane proteins. Although the bulk, spontaneous assembly of vesicles and larger silica nanoparticles (>100 nm) robustly yields SSLBs, it will only occur with low charge density vesicles for smaller nanoparticles (<100 nm), a fundamental barrier in increasing SSLB utility and efficacy. Here, through whole mount and cryogenic transmission electron microscopy, we demonstrate that mixing osmotically loaded vesicles with smaller nanoparticles robustly drives the formation of SSLBs with high membrane charge density (up to 60% anionic lipid or 50% cationic lipid). We show that the osmolyte load necessary for SSLB formation is primarily a function of absolute membrane charge density and is not lipid headgroup-dependent, providing a generalizable, tunable approach toward bulk production of highly curved and charged SSLBs with various membrane compositions.

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    Cited By

    This article is cited by 6 publications.

    1. Tian Zeng, Rajendra P. Gautam, Christopher J. Barile, Ying Li, Edmund C. M. Tse. Nitrile-Facilitated Proton Transfer for Enhanced Oxygen Reduction by Hybrid Electrocatalysts. ACS Catalysis 2020, 10 (21) , 13149-13155. https://doi.org/10.1021/acscatal.0c03506
    2. Haoyuan Jing, Yanbin Wang, Parth Rakesh Desai, Kumaran S. Ramamurthi, Siddhartha Das. Formation and Properties of a Self-Assembled Nanoparticle-Supported Lipid Bilayer Probed through Molecular Dynamics Simulations. Langmuir 2020, 36 (20) , 5524-5533. https://doi.org/10.1021/acs.langmuir.0c00593
    3. Peter J. Chung, Qingteng Zhang, Hyeondo Luke Hwang, Alessandra Leong, Piotr Maj, Robert Szczygiel, Eric M. Dufresne, Suresh Narayanan, Erin J. Adams, Ka Yee C. Lee. α-Synuclein Sterically Stabilizes Spherical Nanoparticle-Supported Lipid Bilayers. ACS Applied Bio Materials 2019, 2 (4) , 1413-1419. https://doi.org/10.1021/acsabm.8b00774
    4. Jacopo Cardellini, Andrea Ridolfi, Melissa Donati, Valentina Giampietro, Mirko Severi, Marco Brucale, Francesco Valle, Paolo Bergese, Costanza Montis, Lucrezia Caselli, Debora Berti. Probing the coverage of nanoparticles by biomimetic membranes through nanoplasmonics. Journal of Colloid and Interface Science 2023, 640 , 100-109. https://doi.org/10.1016/j.jcis.2023.02.073
    5. Tian Zeng, Rajendra P. Gautam, Danny H. Ko, Heng-Liang Wu, Ali Hosseini, Ying Li, Christopher J. Barile, Edmund C. M. Tse. Hybrid bilayer membranes as platforms for biomimicry and catalysis. Nature Reviews Chemistry 2022, 6 (12) , 862-880. https://doi.org/10.1038/s41570-022-00433-2
    6. Peter J. Chung, Hyeondo Luke Hwang, Benjamin R. Slaw, Alessandra Leong, Erin J. Adams, Ka Yee C. Lee. The C‐Terminal Domain of α‐Synuclein Confers Steric Stabilization on Synaptic Vesicle‐Like Surfaces. Advanced Materials Interfaces 2020, 7 (14) https://doi.org/10.1002/admi.201902151

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