Nanoparticle induced fusion of lipid membranes
Source abstract
Abstract
Membrane fusion is crucial for infection of enveloped viruses, cellular transport, and drug delivery via liposomes. Nanoparticles can serve as fusogenic agents facilitating such membrane fusion for direct transmembrane transport. However, the underlying mechanisms of nanoparticle-induced fusion and the ideal properties of such nanoparticles remain largely unknown. Here, we used molecular dynamics simulations to investigate the efficacy of spheroidal nanoparticles with different size, prolateness, and ligand interaction strengths to enhance fusion between vesicles. By systematically varying nanoparticle properties, we identified how each parameter affects the fusion process and determined the optimal parameter range that promotes fusion. These findings provide valuable insights for the design and optimization of fusogenic nanoparticles with potential biotechnological and biomedical applications.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Lipid Membrane Structure and Behavior · Gold and Silver Nanoparticles Synthesis and Applications · Nanopore and Nanochannel Transport Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
CEITEC – Central European Institute of Technology, Kamenice 5, 625 00 Brno, Czech Republic
National Centre for Biomolecular Research, Faculty of Science, Masaryk University, Kamenice 5, 625 00 Brno, Czech Republic
Department of Condensed Matter Physics, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic
Funding
H2020 European Research Council · Ministerstvo Školství, Mládeže a Tělovýchovy
References (48)
Show source-provided references
1. Jahn · Cell · 2003 · 112 · 51910.1016/S0092-8674(03)00112-0 ↗
2. Stalder · Semin. Cell Dev. Biol. · 2020 · 107 · 11210.1016/j.semcdb.2020.04.001 ↗
3. Weissenhorn · FEBS Lett. · 2007 · 581 · 215010.1016/j.febslet.2007.01.093 ↗
4. Straubinger · Cell · 1983 · 32 · 106910.1016/0092-8674(83)90291-X ↗
5. Schneck · Proc. Natl. Acad. Sci. U. S. A. · 2012 · 109 · 1440510.1073/pnas.1205811109 ↗
6. Kawamoto · Soft Matter · 2014 · 10 · 304810.1039/c3sm52344f ↗
7. Chernomordik · Nat. Struct. Mol. Biol. · 2008 · 15 · 67510.1038/nsmb.1455 ↗
8. Azimi · Biomolecules · 2023 · 13 · 113010.3390/biom13071130 ↗
9. Tahir · Proc. Natl. Acad. Sci. U. S. A. · 2020 · 117 · 1847010.1073/pnas.1902597117 ↗
10. Canepa · Small · 2023 · 19 · 220712510.1002/smll.202207125 ↗
11. Perez · Langmuir · 2021 · 37 · 1391710.1021/acs.langmuir.1c02492 ↗
12. Rørvig-Lund · Nano Lett. · 2015 · 15 · 418310.1021/acs.nanolett.5b01366 ↗
13. Deserno · Macromol. Rapid Commun. · 2009 · 30 · 75210.1002/marc.200900090 ↗
14. Mirjanian · J. Phys. Chem. B · 2010 · 114 · 1106110.1021/jp1055182 ↗
15. Kabelka · Biophys. J. · 2022 · 121 · 85210.1016/j.bpj.2021.12.035 ↗
16. Kawamoto · J. Chem. Phys. · 2015 · 143 · 24311210.1063/1.4933087 ↗
17. Risselada · Curr. Opin. Struct. Biol. · 2012 · 22 · 18710.1016/j.sbi.2012.01.007 ↗
18. Poojari · Nat. Commun. · 2021 · 12 · 659410.1038/s41467-021-26924-2 ↗
19. Cooke · Phys. Rev. E: Stat., Nonlinear, Soft Matter Phys. · 2005 · 72 · 01150610.1103/PhysRevE.72.011506 ↗
20. Foley · J. Chem. Theory Comput. · 2020 · 16 · 719510.1021/acs.jctc.0c00862 ↗
21. Bruckner · Biophys. J. · 2009 · 97 · 311310.1016/j.bpj.2009.09.025 ↗
22. Wei · Biophys. J. · 2021 · 120 · 233010.1016/j.bpj.2021.04.012 ↗
23. Risselada · Proc. Natl. Acad. Sci. U. S. A. · 2014 · 111 · 1104310.1073/pnas.1323221111 ↗
24. Risselada · Eur. Biophys. J. · 2020 · 50 · 27910.1007/s00249-020-01484-3 ↗
25. Smirnova · J. Am. Chem. Soc. · 2010 · 132 · 671010.1021/ja910050x ↗
26. Marrink · J. Am. Chem. Soc. · 2003 · 125 · 1114410.1021/ja036138+ ↗
27. Shillcock · Nat. Mater. · 2005 · 4 · 22510.1038/nmat1333 ↗
28. Kasson · PLoS Comput. Biol. · 2010 · 6 · e100082910.1371/journal.pcbi.1000829 ↗
29. Chen · FEBS Lett. · 2007 · 581 · 218110.1016/j.febslet.2007.03.033 ↗
30. Yingchoncharoen · Pharmacol. Rev. · 2016 · 68 · 70110.1124/pr.115.012070 ↗
31. Fulton · Int. J. Mol. Sci. · 2023 · 24 · 661510.3390/ijms24076615 ↗
32. Kim · Drug Delivery Transl. Res. · 2021 · 11 · 140110.1007/s13346-021-00945-2 ↗
33. Herrmann · Nat. Nanotechnol. · 2021 · 16 · 74810.1038/s41565-021-00931-2 ↗
34. Piffoux · ACS Nano · 2018 · 12 · 683010.1021/acsnano.8b02053 ↗
35. Chernomordik · J. Cell Biol. · 2006 · 175 · 20110.1083/jcb.200607083 ↗
36. Brust · J. Chem. Soc., Chem. Commun. · 1994 · 80110.1039/C39940000801 ↗
37. Turkevich · Discuss. Faraday Soc. · 1951 · 11 · 5510.1039/df9511100055 ↗
38. Kundu · Inorg. Chem. · 2008 · 47 · 634410.1021/ic8004135 ↗
39. Jana · Adv. Mater. · 2001 · 13 · 138910.1002/1521-4095(200109)13:18<1389::AID-ADMA1389>3.0.CO;2-F ↗
40. Amina · Int. J. Nanomed. · 2020 · 15 · 982310.2147/IJN.S279094 ↗
41. Pengo · Eur. Biophys. J. · 2017 · 46 · 74910.1007/s00249-017-1250-6 ↗
42. Ferrando · Chem. Rev. · 2008 · 108 · 84510.1021/cr040090g ↗
43. Thompson · Comput. Phys. Commun. · 2022 · 271 · 10817110.1016/j.cpc.2021.108171 ↗
44. Dunweg · Int. J. Mod. Phys. C · 1991 · 02 · 81710.1142/S0129183191001037 ↗
45. Grønbech-Jensen · Comput. Phys. Commun. · 2014 · 185 · 52410.1016/j.cpc.2013.10.006 ↗
46. Weeks · J. Chem. Phys. · 1971 · 54 · 523710.1063/1.1674820 ↗
47. Sapay · Soft Matter · 2009 · 5 · 329510.1039/b902376c ↗
48. Bennett · Biophys. J. · 2014 · 106 · 21010.1016/j.bpj.2013.11.4486 ↗