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Revealing the Structural Intricacies of Biomembrane-Interfaced Emulsions with Small- and Ultra-Small-Angle Neutron Scattering

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posted on 2024-10-21, 21:42 authored by Mark VidallonMark Vidallon, Ashley P Williams, Mitchell J Moon, Haikun Liu, Sylvain Trepout, Alexis I Bishop, Boon Mian Teo, Rico F Tabor, Karlheinz PeterKarlheinz Peter, Liliana de Campo, Xiaowei WangXiaowei Wang
Utilizing cell membranes from diverse cell types for biointerfacing has demonstrated significant advantages in enhancing colloidal stability and incorporating biological properties, tailored specifically for various biomedical applications. However, the structures of these materials, particularly emulsions interfaced with red blood cell (RBC) or platelet (PLT) membranes, remain an underexplored area. This study systematically employs small- and ultra-small-angle neutron scattering (SANS and USANS) with contrast variation to investigate the structure of emulsions containing perfluorohexane within RBC (RBC/PFH) and PLT membranes (PLT/PFH). The findings reveal that the scattering length density of RBC and PLT membranes is 1.5 × 10−6 Å−2, similar to 30% (w/w) deuterium oxide. Using this solvent as a cell membrane-matching medium, estimated droplet diameters are 770 nm (RBC/PFH) and 1.5 µm (PLT/PFH), based on polydispersed sphere model fitting. Intriguingly, calculated patterns and invariant analysis reveal native droplet architectures featuring entirely liquid PFH cores, differing significantly from the observed bubble–droplet core system in electron microscopy. This highlights the advantage of SANS and USANS in differentiating genuine colloidal structures in complex dispersions. In summary, this work underscores the pivotal role of SANS and USANS in characterizing biointerfaced colloids and in uncovering novel colloidal structures with significant potential for biomedical applications and clinical translation.

Funding

The authors acknowledge the support of the Australian Nuclear Science and Technology Organisation (ANSTO), in providing the Bilby SANS and Kookaburra USANS instruments and facilities used in this work (P13738 and P14146). This work also benefited from the use of the SasView application, originally developed under NSF award (DMR-0520547). SasView contains code developed with funding from the European Union's Horizon 2020 research and innovation Program under the SINE2020 project, grant agreement no. (654000). The authors also acknowledge the use of the instruments and scientific and technical assistance at the Ramaciotti Centre for Cryo-Electron Microscopy, a Node of Microscopy Australia. M.L.P.V. was supported by National Heart Foundation of Australia Postdoctoral Fellowship. A.W. was supported by the Australian Government through a Research Training Program (RTP) scholarship; H.L. was supported by the University of Melbourne through a Baker Department of Cardiometabolic Health PhD Scholarship; A.W. and H.L. were supported by AINSE Ltd. through the Postgraduate Research Award (AINSE PGRA) program; K.P. was supported by an NHMRC L3 Investigator Fellowship; X.W. was supported by National Heart Foundation of Australia Future Leader and Baker Fellowships.

History

Publication Date

2024-10-18

Journal

Small Methods

Volume

8

Issue

10

Article Number

2400348

Pagination

13p.

Publisher

Wiley

ISSN

2366-9608

Rights Statement

© 2024 The Author(s). Small Methods published by Wiley-VCH GmbH. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.