Source abstract
Abstract
By reverting to spectroscopy, changes in the biological environment of a fluorescent probe can be monitored and the presence of various phases of the surrounding lipid bilayer membranes can be detected. However, it is currently not always clear in which phase the probe resides. The well-known orange 1,1′-dioctadecyl-3,3,3′,3′-tetramethylindodicarbo-cyanine perchlorate (DiI-C18(5)) fluorophore, for instance, and the new, blue BODIPY (4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) derivative were experimentally seen to target and highlight identical parts of giant unilamellar vesicles of various compositions, comprising mixtures of dipalmitoylphosphatidylcholine (DPPC), dioleoylphosphatidylcholine (DOPC), sphingomyelin (SM), and cholesterol (Chol). However, it was not clear which of the coexisting membrane phases were visualized (Bacalum et al., Langmuir. 2016, 32, 3495). The present study addresses this issue by utilizing large-scale molecular dynamics simulations and the z-constraint method, which allows evaluating Gibbs free-energy profiles. The current calculations give an indication why, at room temperature, both BODIPY and DiI-C18(5) probes prefer the gel (So) phase in DOPC/DPPC (2:3 molar ratio) and the liquid-ordered (Lo) phase in DOPC/SM/Chol (1:2:1 molar ratio) mixtures. This study highlights the important differences in orientation and location and therefore in efficiency between the probes when they are used in fluorescence microscopy to screen various lipid bilayer membrane phases. Dependent on the lipid composition, the angle between the transition-state dipole moments of both probes and the normal to the membrane is found to deviate clearly from 90°. It is seen that the DiI-C18(5) probe is located in the headgroup region of the SM/Chol mixture, in close contact with water molecules. A fluorescence anisotropy study also indicates that DiI-C18(5) gives rise to a distinctive behavior in the SM/Chol membrane compared to the other considered membranes. The latter behavior has not been seen for the studied BODIPY probe, which is located deeper in the membrane.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Department of Theoretical Chemistry and Biology, KTH Royal Institute of Technology, Roslagstullsbacken 15, S-106 91 Stockholm, Sweden
Biomedical Research Institute, Hasselt University, Agoralaan Building C, 3590 Diepenbeek, Belgium
LCSN-EA1069, Faculty of Pharmacy, Limoges University, 2 rue du Dr. Marcland, 87025 Limoges Cedex, France
Centre of New Technologies, University of Warsaw, Banacha 2C, 02-097 Warsaw, Poland
Faculty of Pharmacy, INSERM UMR 1248, Limoges University, 2 rue du Docteur Marcland, 87025 Limoges Cedex, France
Centre of Advanced Technologies and Materials, Faculty of Science, Palacký University, tř. 17 listopadu 12, 771 46 Olomouc, Czech Republic
Funding
Ministerstvo ?kolstv?, Ml?de?e a Telov?chovy · Narodowe Centrum Nauki · H2020 Marie Sklodowska-Curie Actions · Fonds De La Recherche Scientifique - FNRS · Nordic Institute for Theoretical Physics · Center for Quantum Materials · Czech Science Foundation