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Sphingomyelins and ent-Sphingomyelins Form Homophilic Nano-Subdomains within Liquid Ordered Domains.
Yano, Yo; Hanashima, Shinya; Tsuchikawa, Hiroshi; Yasuda, Tomokazu; Slotte, J Peter; London, Erwin; Murata, Michio.
Affiliation
  • Yano Y; Department of Chemistry, Graduate School of Science, Osaka University, Osaka, Japan; ERATO, Lipid Active Structure Project, Japan Science and Technology Agency, Graduate School of Science, Osaka University, Osaka, Japan.
  • Hanashima S; Department of Chemistry, Graduate School of Science, Osaka University, Osaka, Japan.
  • Tsuchikawa H; Department of Chemistry, Graduate School of Science, Osaka University, Osaka, Japan.
  • Yasuda T; Department of Chemistry, Graduate School of Science, Osaka University, Osaka, Japan.
  • Slotte JP; Biochemistry, Faculty of Science and Engineering, Åbo Akademi University, Turku, Finland.
  • London E; Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, New York. Electronic address: erwin.london@stonybrook.edu.
  • Murata M; Department of Chemistry, Graduate School of Science, Osaka University, Osaka, Japan; ERATO, Lipid Active Structure Project, Japan Science and Technology Agency, Graduate School of Science, Osaka University, Osaka, Japan. Electronic address: murata@chem.sci.osaka-u.ac.jp.
Biophys J ; 119(3): 539-552, 2020 08 04.
Article in En | MEDLINE | ID: mdl-32710823
ABSTRACT
Sphingomyelin (SM), a major component of small domains (or lipid rafts) in mammalian cell membranes, forms a liquid-ordered phase in the presence of cholesterol (Cho). However, the nature of molecular interactions within the ordered SM/Cho phase remains elusive. We previously revealed that stearoyl-SM (SSM) and its enantiomer (ent-SSM) separately form nano-subdomains within the liquid-ordered phase involving homophilic SSM-SSM and ent-SSM-ent-SSM interactions. In this study, the details of the subdomain formation by SSMs at the nanometer range were examined using Förster resonance energy transfer (FRET) measurements in lipid bilayers containing SSM and ent-SSM, dioleoyl-phosphatidylcholine and Cho. Although microscopy detected a stereochemical effect on partition coefficient favoring stereochemically homophilic interactions in the liquid-ordered state, it showed no significant difference in large-scale liquid-ordered domain formation by the two stereoisomers. In contrast to the uniform domains seen microscopy, FRET analysis using fluorescent donor- and acceptor-labeled SSM showed distinct differences in SM and ent-SM colocalization within nanoscale distances. Donor- and acceptor-labeled SSM showed significantly higher FRET efficiency than did donor-labeled SSM and acceptor-labeled ent-SSM in lipid vesicles composed of "racemic" (11) mixtures of SSM/ent-SSM with dioleoylphosphatidylcholine and Cho. The difference in FRET efficiency indicated that SSM and ent-SSM assemble to form separate nano-subdomains. The average size of the subdomains decreased as temperature increased, and at physiological temperatures, the subdomains were found to have a single-digit nanometer radius. These results suggest that (even in the absence of ent-SM) SM-SM interactions play a crucial role in forming nano-subdomains within liquid-ordered domains and may be a key feature of lipid microdomains (or rafts) in biological membranes.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phosphatidylcholines / Sphingomyelins Limits: Animals Language: En Journal: Biophys J Year: 2020 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phosphatidylcholines / Sphingomyelins Limits: Animals Language: En Journal: Biophys J Year: 2020 Document type: Article Affiliation country: Japan
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