4.6 Article

Lipid Hydroperoxide Compromises the Membrane Structure Organization and Softens Bending Rigidity

期刊

LANGMUIR
卷 37, 期 33, 页码 9952-9963

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.1c00830

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资金

  1. Sao Paulo Research Foundation (FAPESP) [2014/20107-7]
  2. Fundacao para a Ciencia e a Tecnologia, Portugal (FCT) [FAPESP/20107/2014, PTDC/BTM-SAL/31057/2017, UIDB/04565/2020, PTDC/BIA-BFS/30959/2017]
  3. CNPq
  4. FCT CEEC-Individual Call [CEECIND/00884/2017]
  5. Coordination for the Improvement of Higher Education Personnel (CAPES)
  6. Science without Borders Program
  7. [IST-ID/105/2018]
  8. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [14/20107-7] Funding Source: FAPESP
  9. Fundação para a Ciência e a Tecnologia [PTDC/BIA-BFS/30959/2017, FAPESP/20107/2014, PTDC/BTM-SAL/31057/2017] Funding Source: FCT

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The study investigated the structural and dynamic changes induced by hydroperoxidized lipids in fluid membranes. The results show that the hydroperoxide group decreases lipid bilayer bending rigidity and increases the swelling and hydration between stacked bilayers, indicating alterations in membrane organization.
Lipid hydroperoxides are key mediators of diseases and cell death. In this work, the structural and dynamic perturbations induced by the hydroperoxidized POPC lipid (POPC-OOH) in fluid POPC membranes, at both 23 and 37 degrees C, were addressed using advanced small-angle X-ray scattering (SAXS) and fluorescence methodologies. Notably, SAXS reveals that the hydroperoxide group decreases the lipid bilayer bending rigidity. This alteration disfavors the bilayer stacking and increases the swelling inbetween stacked bilayers. We further investigated the changes in the apolar/ polar interface of hydroperoxide-containing membranes through timeresolved fluorescence/anisotropy experiments of the probe TMA-DPH and time-dependent fluorescence shifts of Laurdan. A shorter mean fluorescence lifetime for TMA-DPH was obtained in enriched POPC-OOH membranes, revealing a higher degree of hydration near the membrane interface. Moreover, a higher microviscosity near TMA-DPH and lower order are predicted for these oxidized membranes, at variance with the usual trend of variation of these two parameters. Finally, the complex relaxation process of Laurdan in pure POPC-OOH membranes also indicates a higher membrane hydration and viscosity in the close vicinity of the -OOH moiety. Altogether, our combined approach reveals that the hydroperoxide group promotes alterations in the membrane structure organization, namely, at the level of membrane order, viscosity, and bending rigidity.

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